
Specialty Topics · Emerging research topic
Microbiome Research and Mental Health
Microbiome research and mental health (gut microbes, probiotics, prebiotics, diet, fecal transplants and stool tests studied for depression and anxiety) · also called Gut-brain axis research, psychobiotics, microbiome and depression, microbiome and anxiety, eje intestino-cerebro, microbioma y salud mental
Researchers ask whether the microbes in the gut influence mood and whether changing them could help depression and anxiety. Studies find differences in gut microbes between groups, but not that microbes cause these conditions. Probiotics show small to large symptom drops in some reviews with low certainty, prebiotics and fermented foods are unproven, fecal transplant is a medical procedure with one early depression trial, and consumer stool tests cannot diagnose anything. None of this is a replacement for mental health care.
General information, not medical advice. Last substantive update · Not medically reviewed. A named clinician has not signed off on this page. How this page is made
About Microbiome Research and Mental Health
Microbiome Research and Mental Health is a research topic, not a treatment. Studies of gut microbes find group differences in depression and anxiety, but not cause. Probiotics have small to large effects on symptom scores in some reviews with low certainty, prebiotics and fermented foods are unproven, fecal transplant is a medical procedure with one early depression trial, and consumer microbiome tests cannot diagnose these conditions. It is not a replacement for care.
What microbiome research and mental health means
Your gut is home to trillions of microbes. A 2019 review says they may communicate with the brain through the immune system, tryptophan metabolism, the vagus nerve and the nervous system of the gut, using chemicals such as short-chain fatty acids. Much of the work that built this idea was done in animals, and human studies are still catching up.
This page covers what studies of gut microbes, probiotics, "psychobiotics" and fecal transplants show about depression and anxiety, what they do not show, and why the research is not a replacement for care. It is about a research idea, not a treatment. It does not cover prescription medicines.
"Psychobiotic" was introduced in 2013 for a live organism that, taken in adequate amounts, gives a health benefit in people with psychiatric illness. In 2016 the term was widened to include prebiotics, and the authors noted that knowledge of how the microbiome responds to outside influence is still limited.
Gut microbe differences in depression and anxiety: association, not cause
A 2021 review and meta-analysis of 59 case-control studies found a shared pattern across depression, bipolar disorder, schizophrenia and anxiety: fewer butyrate-producing bacteria (Faecalibacterium and Coprococcus) and more Eggerthella, with little sign that the pattern is specific to one condition. A large Flemish study of 1,054 people found Coprococcus and Dialister depleted in depression even after correcting for antidepressants.
The weak point is confounding. Reviews of anxiety and depression ask for better handling of diet and psychiatric medicines, which also change gut microbes. A 2025 review found conflicting results on which bacteria were more or less common, and 20 of its 24 studies were in China. Diversity findings were inconsistent.
A group difference also cannot tell you the direction. Microbes might affect mood, mood and its effects on sleep, diet and medicines might change microbes, or both. A systematic review of rodent studies that transferred microbes from ill people found 95% (36 of 38) reported disease features transferring, which the authors called implausibly high.
Probiotics and "psychobiotics" for depression and anxiety: what trials show
A 2019 meta-analysis of 34 controlled trials found small effects of probiotics on depression (d = -0.24) and anxiety (d = -0.10), with larger effects in clinical samples. A 2025 meta-analysis of 23 trials in 1,401 diagnosed patients reported larger drops (depression SMD -0.96, anxiety SMD -0.59) with high heterogeneity. A 2023 review of seven trials in major depression found only modest effects and no consistent change in gut microbe diversity. A 2025 analysis of six trials in unmedicated adults found a small effect (SMD -0.38) that was no longer significant when industry-funded trials were excluded.
The reviews differ because they include different trials, products and people. Trials are short, mostly up to eight weeks, and strains, amounts and products vary. NCCIH says that in most instances we still do not know which probiotics are helpful and which are not. The result is low-certainty evidence that some products may modestly lower symptom scores in some people, not a recommendation.
Prebiotics, Mediterranean-style diet and fermented foods
Prebiotics did not differ from placebo for depression or anxiety in the 2019 meta-analysis, and the 2025 analysis found no significant effect on depression.
In the SMILES trial, 67 adults with moderate to severe depression had either seven dietitian sessions or social support for 12 weeks. Depression scores fell more with diet support and remission was 32.3% versus 8.0%. A 2025 meta-analysis of five Mediterranean diet trials also found lower scores, but rated the evidence low certainty with very high heterogeneity.
A four-week diet high in fermented and prebiotic foods lowered perceived stress by 32% versus 17% in healthy adults, but the groups did not differ significantly. A survey of 710 young adults linked fermented food intake with less social anxiety in people high in neuroticism, which cannot show cause.
Fecal microbiota transplant for depression: early research only
Fecal microbiota transplant (FMT) moves microbes from a healthy donor into a patient. Its established use is for recurrent Clostridioides difficile infection. The FDA page for VOWST lists the indication as preventing recurrence of that infection in adults, not depression.
In a 2026 randomized, double-blind trial in major depression, two weeks of FMT capsules or placebo were added to a standard antidepressant. Remission at week 8 did not differ significantly, although depression scores fell more with FMT at weeks 2 and 8. A 2025 pooled analysis of 12 trials in 681 people, many with irritable bowel syndrome, reported benefit that faded by 6 months. The evidence is small. Serious risks exist (see Safety), and FMT should never be a do-it-yourself project.
Direct-to-consumer microbiome tests: what they cannot tell you
No validated stool test for diagnosing or screening for depression or anxiety was found. A commercial-test dataset from Japan found no significant composition differences among groups based on depression screening scores. A research model in 62 patients with bipolar depression and 60 healthy people reached an area under the curve of 0.733, but it was one study and no independent clinical validation was read.
An international expert panel says commercial microbiome diagnostic tests are offered without consensus on regulation or any proven value in clinical practice. When seven consumer services were tested with the same standard stool material they gave major discrepancies, as large as differences between donors. A test result cannot diagnose depression, anxiety or "gut-caused" mood problems.
Safety first: not a replacement for care
Persistent low mood, anxiety, thoughts of self-harm or changes in sleep and appetite need assessment by a health professional. NIMH says treatment usually includes therapy, medication or both. NCCIH says not to use probiotics as a reason to postpone seeing your health care provider. Do not stop or change prescribed medicine for a probiotic, diet or test result without the prescriber.
Probiotics have a long record of apparently safe use in healthy people, but NCCIH says the risk of harm is greater in severe illness or weakened immunity, and bloodstream infections with probiotic organisms have been reported, mostly in children with central venous catheters. FMT carries risks too: two patients developed drug-resistant bloodstream infection from one donor and one died.
If you are thinking about harming yourself, contact local emergency services or a crisis line in your country, or go to the nearest emergency department. NIMH lists 911 and, in the US, 988 (call or text).
At a glance
Traditional uses history, not proof
Studied for research
- Probiotic supplements for depression, low certainty
- Probiotic supplements for anxiety, very low certainty
- Prebiotic fibres, insufficient
- Mediterranean-style diet for depression, low certainty
- Fermented foods and psychobiotic diets, insufficient
- Fecal microbiota transplant, insufficient
- Stool tests to diagnose depression, evidence against
Main compounds
- Probiotics
- Prebiotics
- Diet pattern
- Fermented foods
- Fecal microbiota transplant
- Stool microbiome tests
Common forms
- Capsules and sachets of live organisms
- Dietary programmes
- Fermented foods
- Clinic-delivered capsules, enemas or endoscopy (FMT)
Research links: Meta-analysis of prebiotic and probiotic trials for depression and anxiety (34 trials) · Meta-analysis of gut microbiota perturbations in psychiatric disorders (59 studies) · SMILES dietary improvement trial in major depression · Adjunctive FMT trial in major depression, 2026 · International consensus on microbiome testing in clinical practice · Research Library · Genes & Biomarkers Library
What it is and its history
- Accepted scientific name
- Microbiome research and mental health (a research topic, not a condition or a treatment)
- Common names
- Gut-brain axis research (English); Psychobiotics (English); Microbiota-gut-brain axis (English); Eje intestino-cerebro (Spanish); Microbioma y salud mental (Spanish)
- Look-alikes and adulterants
- Name: Probiotic supplements; Note: The products most often tested; see the probiotic supplements guide on this site.; Name: Depression and anxiety disorders; Note: The conditions studied; they have their own condition pages and established care described by NIMH and others.; Name: Irritable bowel syndrome; Note: A gut condition in which psychobiotics were first studied and which mixes into several FMT trials.
What is inside, and how it may work
What it contains and how those compounds act in cells and animals. Laboratory and animal mechanisms are not proven effects in people.
Main compounds
| Compound | Family | Where it is concentrated | Activity studied | Level of evidence |
|---|---|---|---|---|
| Probiotic supplements | live microorganisms | Studied as capsules or sachets, usually Lactobacillus and Bifidobacterium. Results vary widely by review. 14 1 17 11 7 | Human data | |
| Prebiotic fibres | food for gut microbes | Did not differ from placebo for depression or anxiety in the meta-analyses read. 14 1 | Human data | |
| Diet pattern (Mediterranean-style) and fermented foods | diet | A dietitian-led programme in the SMILES trial and a meta-analysis of five Mediterranean diet trials found lower depression scores; low certainty. A fermented-food diet did not beat control for stress in healthy adults. 10 3 2 | Human data | |
| Fecal microbiota transplantation | microbial transfer (medical procedure) | One randomized trial in depression plus a mixed meta-analysis; approved by FDA only for preventing recurrent C. difficile infection (VOWST page). 13 26 31 | Human data | |
| Direct-to-consumer stool tests | testing | Not validated for diagnosing depression or anxiety. 19 22 15 | Human data |
Mechanisms, receptors and pathways
| Target or pathway | Gene or receptor | What was found | Level |
|---|---|---|---|
| Communication routes between gut and brain | The 2019 review lists the immune system, tryptophan metabolism, the vagus nerve and the enteric nervous system, and microbial products such as short-chain fatty acids, branched chain amino acids and peptidoglycans. This is a description of proposed routes, largely from animal work. 29 | Animal and review | |
| Loss of butyrate-producing, anti-inflammatory bacteria | The 2021 meta-analysis suggests these disorders show a reduction of anti-inflammatory butyrate-producing bacteria and enrichment of pro-inflammatory ones. This is a pattern in groups, not a shown cause. 18 24 | Observational | |
| Psychobiotic action on the brain-gut axis | The 2013 paper proposes that some bacteria produce neuroactive substances such as GABA and serotonin and may act through the vagus nerve, spinal cord or neuroendocrine systems. At that time evidence came from rodents. 27 28 | Rodent (background) | |
| Bile acids and inflammation (FMT trial) | In the 2026 trial the authors report a bile-acid-linked suppression of inflammatory pathways in a mediation analysis; this is a statistical link in one trial. 13 | Human (mediation analysis) | |
| Caution about causal claims from rodent transfer studies | A systematic review found 95% of human microbiota-associated rodent studies (36 of 38) reported transfer of disease features and called this implausibly high, saying it overstates the role of the microbiome in human disease. 30 | Systematic review of animal studies |
Isolated compounds versus whole extracts
Probiotic supplements, prebiotic fibres, fermented foods and whole-diet changes are different interventions. NCCIH says different types of probiotics may have different effects, and what helps for one kind of Lactobacillus does not necessarily apply to another. Food-based changes act on many things at once, so a diet trial cannot tell which part worked.
2 low certainty1 very low certainty3 not enough evidence1 evidence against
What was looked at
The 7 benefits and uses checked for Microbiome Research and Mental Health, each with how strong the evidence is. Tap one to open it.
- Probiotic supplements for depression symptomsLow certainty
- Probiotic supplements for anxiety symptomsVery low certainty
- Prebiotic fibres for depression and anxietyNot enough evidence
- Dietary improvement (Mediterranean-style) for depressionLow certainty
- Fermented foods and "psychobiotic" diets for stress, anxiety and moodNot enough evidence
- Fecal microbiota transplant (FMT) for depressionNot enough evidence
- Stool microbiome tests to diagnose or predict depressionEvidence against
Lab markers tracked in the studies
Gut microbe composition (stool microbiome)Depression symptom scoresAnxiety symptom scoresPerceived stress scoreRemission and HAMD-17 depression scoreAccuracy of microbiome-based classifiers (AUC)
What is Microbiome Research and Mental Health good for?
The main ways gut microbes have been studied for depression and anxiety, and how strong the human evidence is for each. These describe what studies found in the groups they studied. They are not advice to use any approach, they are not a replacement for mental health care, and each result applies to the product or programme tested.
Benefits, one by one
Each card is a research question, not a promise. Tap a goal to filter. Open a card to see the studies, doses and limits.
Probiotic supplements for depression symptoms
Low certaintySeveral reviews of trials found small to large drops in depression scores with probiotics compared with placebo, but the reviews disagree on size, the trials were short and varied, and one analysis lost its effect once industry-funded trials were removed. Probiotics are not an established treatment for depression.
6 studiesThe trials used many different products, mostly Lactobacillus and Bif…
Studies, doses and limits
What the trials found
Reviews of controlled trials: 34 trials (2019 meta-analysis), 23 trials in 1,401 diagnosed patients (2025), 7 trials in major depressive disorder (2023), 13 trials in 437 adults (2026) and 6 trials in 341 unmedicated adults (2025).
Results
The 2019 meta-analysis found a small effect (d = -0.24), larger in clinical samples. The 2025 analysis of diagnosed patients found a large pooled drop (SMD -0.96) with high heterogeneity. The 2023 review found only modest effects. The 2026 review found most trials improved, mostly in mild to moderate outpatients with multi-strain products. In unmedicated adults the effect was small (SMD -0.38) and not significant once industry-funded trials were excluded.
Effect sizes as reported
d -0.24 (2019); SMD -0.96, CI -1.31 to -0.61 (2025); SMD -0.38, CI -0.57 to -0.18 (2025, unmedicated); SMD -0.21, CI -0.65 to 0.23 after excluding industry-funded trials.
Why this rating
Compiler's rating: low. The effect direction agrees across reviews, but size varies a lot, trials are short (mostly up to 8 weeks), strains and products differ, diet was rarely controlled, adverse events were poorly reported and part of the evidence is industry-funded.
Form and dose studied
The trials used many different products, mostly Lactobacillus and Bifidobacterium, often multi-strain, for about 4 to 8 weeks. This describes what was studied, not what anyone should take. NCCIH says that in most instances we still do not know which probiotics are helpful and which are not.
Who was studied
Adults with depression, from mild symptoms to major depressive disorder, mostly outpatients; some trials were in people also taking antidepressants.
Limits
Short trials, many strains, different countries, high heterogeneity, small samples, possible industry bias, no good long-term data.
Why researchers looked
The gut microbe differences seen in depression led researchers to test whether live bacteria in supplements could change mood.
Proposed mechanism Hypothesis
Proposed only: probiotics might act through the immune system, gut chemicals or the vagus nerve. The trials read measured symptoms, and one review found no consistent change in gut microbe diversity or composition after 4 to 8 weeks.
A proposed mechanism does not show that the effect happens in people.
Probiotics can cause serious infections in a few very ill people (see the Safety tab). They are not a reason to delay care or to change prescribed medicines.
Probiotic supplements for anxiety symptoms
Very low certaintyReviews found small to moderate drops in anxiety scores with probiotics, but fewer trials looked at anxiety than at depression, and for diagnosed anxiety disorders there is almost nothing. Probiotics are not an established treatment for anxiety.
3 studiesMany different products and strains, usually for several weeks; not a…
Studies, doses and limits
What the trials found
The 2019 meta-analysis of 34 trials and the 2025 meta-analysis of 23 trials in diagnosed patients (9 trials of probiotics for anxiety). A 2024 review of 42 studies in psychiatric diagnoses found only one study in generalized anxiety disorder.
Results
Probiotics had a very small effect on anxiety in the 2019 meta-analysis (d = -0.10, p = .03) and a moderate effect in the 2025 analysis (SMD -0.59) with high heterogeneity. The 2024 review said that, except in major depression, evidence does not clarify the role of probiotics in mental illness.
Effect sizes as reported
d -0.10 (2019); SMD -0.59, CI -0.98 to -0.19 (2025)
Why this rating
Compiler's rating: very low. The two meta-analyses differ about six-fold in size, anxiety trials are few and short, and diagnosed anxiety disorders were barely studied.
Form and dose studied
Many different products and strains, usually for several weeks; not advice on what to take.
Who was studied
Mixed groups: people with depression and anxiety symptoms, medical and community samples. Almost no data in diagnosed generalized anxiety disorder.
Limits
Few trials, wide size differences, short follow-up, high heterogeneity.
Why researchers looked
Anxiety often goes with depression, and animal work suggested gut bacteria influence stress responses, so trials added anxiety as an outcome.
Proposed mechanism Hypothesis
Proposed only, as for depression.
A proposed mechanism does not show that the effect happens in people.
Same cautions as for depression. Established care for anxiety disorders is on the anxiety page.
Prebiotic fibres for depression and anxiety
Not enough evidencePrebiotics (food for gut bacteria) did not beat placebo on depression or anxiety in the two meta-analyses that tested them. Evidence is too thin to say they help.
2 studiesNot described in the abstracts in plain units. The review called preb…
Studies, doses and limits
What the trials found
2019 meta-analysis of 34 trials (prebiotic arms) and a 2025 meta-analysis with 3 prebiotic trials in depression.
Results
Prebiotics did not differ from placebo for depression (d = -0.08, p = .51) or anxiety (d = 0.12, p = .11) in 2019. In 2025, depression SMD was -0.28 with a confidence interval that included no effect.
Effect sizes as reported
d -0.08 and 0.12 (2019); SMD -0.28, CI -0.61 to 0.04 (2025)
Why this rating
Compiler's rating: insufficient. Neither review found a significant effect, and only 3 prebiotic trials in depression were pooled in 2025.
Form and dose studied
Not described in the abstracts in plain units. The review called prebiotics food components that feed gut microbes.
Who was studied
Adults with depression or anxiety symptoms.
Limits
Very few trials; the 2025 authors still call for more research.
Why researchers looked
Prebiotics were tested as a way to feed the gut bacteria seen to be low in depression.
Proposed mechanism Hypothesis
Proposed only: feeding butyrate-producing bacteria. Not tested in these trials.
A proposed mechanism does not show that the effect happens in people.
Fibre-rich foods are a normal part of diet; added prebiotic powders can cause gas or bloating in some people (general knowledge, not from a source read).
Dietary improvement (Mediterranean-style) for depression
Low certaintyOne small 12-week trial (SMILES) found that dietitian-led dietary support lowered depression scores more than social support, and a review of five trials found lower scores too, but the review rated the evidence low certainty and the trials differ a lot.
2 studiesSMILES used seven sessions with a clinical dietitian over 12 weeks, a…
Studies, doses and limits
What the trials found
SMILES: 67 adults with moderate to severe depression for 12 weeks (diet 33, control 34). Meta-analysis: 5 randomized trials, 1,507 adults.
Results
In SMILES the MADRS fell more with diet support (Cohen's d -1.16), and remission was 32.3% versus 8.0%. The 2025 meta-analysis found lower depressive symptoms with Mediterranean diet interventions (SMD -0.53) but very high heterogeneity (87.1%) and a prediction interval that includes no effect.
Effect sizes as reported
SMILES d -1.16, remission 10 of 31 vs 2 of 25; meta-analysis SMD -0.53, CI -0.90 to -0.16.
Why this rating
Compiler's rating: low, matching the review authors' own GRADE rating. One small single-blind trial and a heterogeneous set of five trials; most participants in SMILES also had other treatment.
Form and dose studied
SMILES used seven sessions with a clinical dietitian over 12 weeks, as an add-on to other care. Its protocol paper is titled as a modified Mediterranean dietary intervention (title only read). This describes the trial, not a prescription.
Who was studied
Adults with moderate to severe depression (SMILES); adults aged about 22 to 53 with depression in the meta-analysis.
Limits
Small samples, single blind, very high heterogeneity, only one trial with remission data read, no long-term follow-up read.
Why researchers looked
Diet affects gut microbes and general health, and people with depression often eat poorly, so researchers tested diet change as a supportive step.
Proposed mechanism Hypothesis
Proposed only: diet might act through gut microbes, inflammation or general health. The trials read did not test these routes.
A proposed mechanism does not show that the effect happens in people.
Diet change is a supportive step, not a replacement for therapy or medicines. People with food allergies, eating disorders or medical diets should plan changes with a clinician.
Fermented foods and "psychobiotic" diets for stress, anxiety and mood
Not enough evidenceA four-week diet high in fermented and prebiotic foods lowered perceived stress in healthy adults, but not more than the control diet. A survey linked fermented food intake with less social anxiety in people high in neuroticism. This is not enough to say fermented foods help mood.
4 studiesThe trial diet was high in prebiotic and fermented foods for 4 weeks;…
Studies, doses and limits
What the trials found
One randomized trial in 45 healthy adults (4 weeks), one survey of 710 young adults, and a 2024 review of 42 clinical studies that included fermented foods in its search.
Results
In the trial perceived stress fell by 32% versus 17%, but the groups did not differ significantly; higher adherence went with bigger drops. In the survey, fermented food intake linked to fewer social anxiety symptoms only for people high in neuroticism. The 2024 review could not clarify a role outside depression.
Effect sizes as reported
Trial: 32% vs 17% reduction, not significant between groups. Survey: interaction effect, no number in the abstract.
Why this rating
Compiler's rating: insufficient. One small trial in healthy people that missed its between-group comparison, plus one survey that cannot show cause.
Form and dose studied
The trial diet was high in prebiotic and fermented foods for 4 weeks; the survey measured how often people ate fermented foods. These describe what was studied.
Who was studied
Healthy adults (trial); young adults (survey).
Limits
Small, short, healthy participants, self-report, cannot show cause.
Why researchers looked
Fermented foods and fibre feed or add gut microbes, so researchers asked whether eating them could be a food-based form of a probiotic.
Proposed mechanism Hypothesis
Proposed only: more diverse microbes and their by-products. In the trial, microbial composition changed only subtly.
A proposed mechanism does not show that the effect happens in people.
Fermented foods are ordinary foods for most people, but some (such as very salty or aged products) do not suit everyone; people with weakened immune systems should ask their clinician (general guidance; see Safety).
Fecal microbiota transplant (FMT) for depression
Not enough evidenceA 2026 trial of FMT capsules added to an antidepressant found no difference in remission at 8 weeks, although depression scores fell more in the transplant group, and a 2025 pooled analysis found benefit that faded by 6 months. FMT is not an approved treatment for depression and is a medical procedure.
5 studiesThe trial used FMT capsules for 2 weeks. Meta-analysed trials used ca…
Studies, doses and limits
What the trials found
One randomized, double-blind trial in major depression; a 2025 meta-analysis of 12 randomized trials (681 participants, many with irritable bowel syndrome); a 2020 systematic review that mostly covers animal work.
Results
In the 2026 trial remission at week 8 did not differ, but HAMD-17 scores fell more at weeks 2 and 8. The 2025 meta-analysis found a large pooled reduction (SMD -1.21) that fell to -0.56 in a sensitivity analysis and diminished by 6 months; the effect was smaller in people with neurological or psychiatric conditions (SMD -0.67).
Effect sizes as reported
SMD -1.21, CI -1.87 to -0.55; sensitivity SMD -0.56, CI -0.86 to -0.26; trial remission not significant.
Why this rating
Compiler's rating: insufficient. Only one randomized depression trial was read and its main outcome was null; the pooled analysis mixes in gut disease and shows fading effects. Evidence is small.
Form and dose studied
The trial used FMT capsules for 2 weeks. Meta-analysed trials used capsules, endoscopy or enemas. FMT is given by clinicians in controlled settings only; this is not advice.
Who was studied
Adults with major depression already taking a standard antidepressant (2026 trial); mixed gut and neuropsychiatric patients (2025).
Limits
One main trial; mixed populations; short follow-up; effects fading by 6 months.
Why researchers looked
Because FMT works for a specific bowel infection, researchers asked whether moving microbes from a healthy donor could also ease mood symptoms.
Proposed mechanism Hypothesis
Proposed: changes in bile acids and inflammation (the trial authors' mediation analysis). This is a statistical link in one trial, not proof.
A proposed mechanism does not show that the effect happens in people.
FMT carries real infection risks and is not available for depression outside trials (see Safety). Do not attempt do-it-yourself transplants.
Stool microbiome tests to diagnose or predict depression
Evidence againstNo validated stool test for depression was found. A commercial-test dataset found no significant composition differences by depression screening score, and research models in bipolar depression have not been shown to work in independent groups.
4 studiesStool samples sequenced in the lab; in research, random forest models…
Studies, doses and limits
What the trials found
Commercial-test dataset analysis in Japan; a case-control study with machine learning in 62 patients and 60 controls; an international expert consensus on microbiome testing (2025).
Results
No significant differences in composition by depression screening score in the commercial dataset. The research model reached an AUC of 0.733 for patients versus controls in a single study. The expert consensus says evidence supporting clinical usefulness of microbiome diagnostics is scarce and that commercial tests lack proven value in clinical practice.
Effect sizes as reported
AUC 0.733 and 0.800 in one research study; no significant differences in the commercial dataset.
Why this rating
Compiler's rating: against. The only independent-looking data found showed no difference, the accurate-looking model was a single-site research study, and an international expert panel says clinical value is unproven.
Form and dose studied
Stool samples sequenced in the lab; in research, random forest models were built from bacterial species.
Who was studied
Adults in Japan using commercial tests; patients with bipolar depression in China (research).
Limits
Small samples, no independent validation read, no clinical diagnoses in the commercial dataset.
Why researchers looked
If microbes differ in depression, perhaps a stool test could flag it or predict who will respond to treatment.
Proposed mechanism Hypothesis
A diagnostic idea rather than a treatment, so no mechanism is proposed.
A proposed mechanism does not show that the effect happens in people.
A test result cannot tell you whether you have depression. See a clinician for assessment.
Connections to the rest of health
How Microbiome Research and Mental Health connects to the rest of our health knowledge graph. Every link says what kind of connection it is. A safety link (for example to the liver) is a warning, not a benefit. A study that merely mentions a topic never creates a benefit link.
Explore every connection: goals, body systems, organs, symptoms, genes
A. Wellness goals
| Connected to | Kind of connection | Evidence status | Context | Studies |
|---|---|---|---|---|
| Mood Balance | Low certainty | Probiotic supplements for depression symptoms: Several reviews of trials found small to large drops in depression scores with probiotics compared with placebo, but the reviews disagree on size, the trials were short and varied, and one analysis lost its effect once industry-funded trials were removed. Probiotics are not an established treatment for depression. | 14 1 17 11 7 32 | |
| Anxiety Support | Very low certainty | Probiotic supplements for anxiety symptoms: Reviews found small to moderate drops in anxiety scores with probiotics, but fewer trials looked at anxiety than at depression, and for diagnosed anxiety disorders there is almost nothing. Probiotics are not an established treatment for anxiety. | 14 1 21 | |
| Mood Balance | Not enough evidence | Prebiotic fibres for depression and anxiety: Prebiotics (food for gut bacteria) did not beat placebo on depression or anxiety in the two meta-analyses that tested them. Evidence is too thin to say they help. Fermented foods and "psychobiotic" diets for stress, anxiety and mood: A four-week diet high in fermented and prebiotic foods lowered perceived stress in healthy adults, but not more than the control diet. A survey linked fermented food intake with less social anxiety in people high in neuroticism. This is not enough to say fermented foods help mood. | 14 1 2 9 21 32 15 12 19 22 | |
| Mood Balance | Low certainty | Dietary improvement (Mediterranean-style) for depression: One small 12-week trial (SMILES) found that dietitian-led dietary support lowered depression scores more than social support, and a review of five trials found lower scores too, but the review rated the evidence low certainty and the trials differ a lot. Fecal microbiota transplant (FMT) for depression: A 2026 trial of FMT capsules added to an antidepressant found no difference in remission at 8 weeks, although depression scores fell more in the transplant group, and a 2025 pooled analysis found benefit that faded by 6 months. FMT is not an approved treatment for depression and is a medical procedure. | 10 3 13 26 5 6 31 | |
| Brain Health | Low certainty | Dietary improvement (Mediterranean-style) for depression: One small 12-week trial (SMILES) found that dietitian-led dietary support lowered depression scores more than social support, and a review of five trials found lower scores too, but the review rated the evidence low certainty and the trials differ a lot. | 10 3 | |
| Gut Health | Not enough evidence | Fermented foods and "psychobiotic" diets for stress, anxiety and mood: A four-week diet high in fermented and prebiotic foods lowered perceived stress in healthy adults, but not more than the control diet. A survey linked fermented food intake with less social anxiety in people high in neuroticism. This is not enough to say fermented foods help mood. | 2 9 21 32 |
B. Body systems
| Connected to | Kind of connection | Evidence status | Context | Studies |
|---|---|---|---|---|
| Nervous System | Biological association | Low certainty | Studied for: Probiotic supplements for depression symptoms Studied for: Probiotic supplements for anxiety symptoms | 14 1 17 11 7 32 21 10 3 13 26 5 6 31 |
| Stress Mood | Biological association | Low certainty | Studied for: Probiotic supplements for depression symptoms Studied for: Probiotic supplements for anxiety symptoms | 14 1 17 11 7 32 21 2 9 |
| Digestive System | Biological association | Not enough evidence | Studied for: Prebiotic fibres for depression and anxiety Studied for: Fermented foods and "psychobiotic" diets for stress, anxiety and mood | 14 1 2 9 21 32 13 26 5 6 31 15 12 19 22 |
| Whole Body | Biological association | Low certainty | Studied for: Dietary improvement (Mediterranean-style) for depression | 10 3 |
E. Health conditions
| Connected to | Kind of connection | Evidence status | Context | Studies |
|---|---|---|---|---|
| Depression | Systematic reviews and trials, low certainty | Small to large symptom drops in some reviews; not established treatments. Preparation or compound: Probiotics, diet, fecal microbiota transplant |
14 1 | |
| Anxiety disorders | Systematic reviews, very low certainty | Very small to moderate effects on anxiety scores; almost no data in diagnosed disorders. Preparation or compound: Probiotics |
14 1 21 | |
| Recurrent C. difficile infection | Randomized trials and regulator approval | The setting where FMT has evidence and approval; not depression. Preparation or compound: Fecal microbiota-based products |
16 31 |
I. Biomarkers
| Connected to | Kind of connection | Evidence status | Context | Studies |
|---|---|---|---|---|
| Gut microbe composition (stool microbiome) | Biological association | Mixed findings | Measured in trials: Group differences, not consistent: often fewer butyrate-producing bacteria (Faecalibacterium, Coprococcus) and more of some pro-inflammatory groups (such as Eggerthella); diversity results conflicted.. A lab change is not the same as a health benefit. | 18 24 23 4 |
| Depression symptom scores | Biological association | Low certainty | Measured in trials: Lower scores with probiotics and diet support in several trials, with large differences between reviews.. A lab change is not the same as a health benefit. | 14 1 7 10 |
| Anxiety symptom scores | Biological association | Very low certainty | Measured in trials: Small to moderate reductions with probiotics in two meta-analyses.. A lab change is not the same as a health benefit. | 14 1 |
| Perceived stress score | Biological association | Not enough evidence | Measured in trials: Fell in both diet groups; the psychobiotic diet did not differ significantly from control.. A lab change is not the same as a health benefit. | 2 |
| Remission and HAMD-17 depression score | Biological association | Not enough evidence | Measured in trials: No significant remission difference at week 8; greater HAMD-17 reduction at weeks 2 and 8 with FMT.. A lab change is not the same as a health benefit. | 13 |
| Accuracy of microbiome-based classifiers (AUC) | Biological association | Very low certainty | Measured in trials: Moderate accuracy in one research study; not tested in independent groups in the sources read.. A lab change is not the same as a health benefit. | 12 |
L. Active compounds
| Connected to | Kind of connection | Evidence status | Context | Studies |
|---|---|---|---|---|
| Probiotic supplements | Biological association | Human | Studied as capsules or sachets, usually Lactobacillus and Bifidobacterium. Results vary widely by review. | 14 1 17 11 7 |
| Prebiotic fibres | Biological association | Human | Did not differ from placebo for depression or anxiety in the meta-analyses read. | 14 1 |
| Diet pattern (Mediterranean-style) and fermented foods | Biological association | Human | A dietitian-led programme in the SMILES trial and a meta-analysis of five Mediterranean diet trials found lower depression scores; low certainty. A fermented-food diet did not beat control for stress in healthy adults. | 10 3 2 |
| Fecal microbiota transplantation | Biological association | Human | One randomized trial in depression plus a mixed meta-analysis; approved by FDA only for preventing recurrent C. difficile infection (VOWST page). | 13 26 31 |
| Direct-to-consumer stool tests | Biological association | Human | Not validated for diagnosing depression or anxiety. | 19 22 15 |
Each connection is stored with the ingredient, the connected record, the kind of connection, the evidence status, the supporting studies, the preparation or compound involved, and a review date (last reviewed October 31, 2026).
Evidence at a glance: what the research found for 7 outcomes
Each outcome below is one thing researchers measured. Certainty is how far the evidence can be trusted, not how well it works. The full studies are on the next tab.
The evidence
The research centre for Microbiome Research and Mental Health. Every record here was checked against PubMed or the publisher's page; we never list a study we have not verified.
Evidence by outcome
Bars show how many studies we found for each outcome, not how well it works. People are added up across trials only (reviews are not added, to avoid double counting).
How we rate evidence
High certainty
Several well-run trials or reviews agree; further research is unlikely to change the picture much.
Moderate certainty
Good trials point the same way, but some doubt remains.
Low certainty
Small, short or inconsistent trials. The finding could change with better research.
Very low certainty
Very little or very weak human data. Treat as a possibility only.
Mixed findings
Trials or reviews disagree with each other.
Not enough evidence
Not enough human research to say either way.
Evidence against
Good research found no benefit, or found harm.
We take the reviewers' own risk-of-bias and GRADE statements where they exist, and otherwise judge from study size, design, consistency, directness and whether a product matches what is sold. Many publications do not make evidence high. Method note: We searched PubMed, read the abstract of every review, trial and study cited, and read the NCCIH, FDA and NIMH pages as downloaded text. Full texts were not read. Certainty ratings are the compiler's own reading unless a review gives its own grade (stated in the text). Funding is not stated in most abstracts, and this is noted where relevant.
Study library: every study we checked 34
| Study | Design | People | Product, dose, length | Result |
|---|---|---|---|---|
| Asad 2025 Effects of Prebiotics and Probiotics on Symptoms of Depression and Anxiety in Clinically Diagnosed Samples: Systematic Review and Meta-analysis of Randomized Controlled Trials. Nutr Rev · PMID 39731509 · DOI |
Systematic review and meta analysis of randomized trials |
23 randomized trials, 1,401 patients with clinically diagnosed depression or anxiety symptoms (20 trials in the meta-analysis) | Probiotics, prebiotics or synbiotics Mostly up to 8 weeks · vs Placebo |
Probiotics lowered depression symptoms (18 trials) and anxiety symptoms (9 trials) more than placebo. Prebiotics (3 trials in depression) did not show a significant effect. Heterogeneity between studies was high; study length and formulation contributed to the differences. Probiotics: depression SMD -0.96, anxiety SMD -0.59. Prebiotics: depression SMD -0.28. (Depression -1.31 to -0.61; anxiety -0.98 to -0.19; prebiotics -0.61 to 0.04) Methods, limits and fundingOutcomes: Depression and anxiety symptom scores Limitations: High heterogeneity; short trials; many different products. Pooled effects this large are unusual for this field and should be read with caution. Funding and conflicts: Funding is not stated in the abstract. Registration: PROSPERO CRD42023424136 Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Berding 2023 Feed your microbes to deal with stress: a psychobiotic diet impacts microbial stability and perceived stress in a healthy adult population. Mol Psychiatry · PMID 36289300 · DOI |
Randomized controlled trial (diet) |
45 45 healthy adults (24 psychobiotic diet, 21 control diet) |
Psychobiotic diet (high in prebiotic and fermented foods) 4 weeks · vs Control diet |
Perceived stress fell 32% on the psychobiotic diet and 17% on the control diet, but the difference between groups was not significant. Stress biomarkers were not affected. Microbial composition changed only subtly. Higher adherence to the diet went with bigger drops in perceived stress. Perceived stress 32% vs 17% reduction; between-group difference not significant (Not given in the abstract) Methods, limits and fundingOutcomes: Perceived stress; stool microbiome; metabolites Limitations: Small, short trial in healthy adults, so it says little about people with depression or anxiety. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Bizzozero-Peroni 2025 The impact of the Mediterranean diet on alleviating depressive symptoms in adults: a systematic review and meta-analysis of randomized controlled trials. Nutr Rev · PMID 38219230 · DOI |
Systematic review and meta analysis of randomized trials |
1507 5 randomized trials, 1,507 young and middle-aged adults with major depression or mild to moderate depressive symptoms |
Mediterranean diet interventions Varied · vs Control conditions |
Mediterranean diet interventions reduced depressive symptoms compared with control conditions. Overall risk of bias ranged from some concerns to high and the certainty of evidence was low. SMD -0.53; I2 87.1%; prediction interval -1.86 to 0.81 (-0.90 to -0.16) Methods, limits and fundingOutcomes: Depressive symptom severity Limitations: Very high heterogeneity, only 5 trials, low certainty by the authors' own GRADE rating. The prediction interval includes no effect. Funding and conflicts: Funding is not stated in the abstract. Registration: PROSPERO CRD42022341895 Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Cao 2025 Gut microbiota variations in depression and anxiety: a systematic review. BMC Psychiatry · PMID 40312666 · DOI |
Systematic review of case control studies |
24 articles; 20 of them conducted in China | Gut microbiota comparisons Cross-sectional · vs People without depression or anxiety |
Diversity findings were inconsistent for both depression and anxiety. Both were characterised by more pro-inflammatory bacteria and fewer anti-inflammatory short-chain fatty acid producers, but reports conflicted because of confounders such as diet and psychotropic medicines. Not given (Not given) Methods, limits and fundingOutcomes: Alpha and beta diversity; taxa abundance Limitations: Mostly one country; conflicting reports; qualitative synthesis only. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Chinna Meyyappan 2020 Effect of fecal microbiota transplant on symptoms of psychiatric disorders: a systematic review. BMC Psychiatry · PMID 32539741 · DOI |
Systematic review human and animal |
21 studies of fecal microbiota transplantation in relation to psychiatric symptoms; the abstract describes clinical, human-donor preclinical and entirely preclinical studies | Fecal microbiota transplantation Varied · vs Varied |
The abstract says all studies found a decrease in depressive and anxiety-like symptoms after transplantation of healthy microbiota, and that depressive and anxiety-like behaviours were transmitted from ill donors to healthy recipients. It concludes the evidence is strong but calls for larger, better-designed studies to establish efficacy and safety. Not pooled (Not pooled) Methods, limits and fundingOutcomes: Mood and behaviour measures Limitations: Most of the evidence is from animals; the counts in the abstract (8 clinical, 9 preclinical with human donors, 11 preclinical) do not add up to 21, so only the existence of a small clinical group is relied on here. The claim of "strong evidence" is not supported by the controlled human data. Funding and conflicts: Funding is not stated in the abstract. Registration: PROSPERO CRD42019126795 Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| DeFilipp 2019 Drug-Resistant E. coli Bacteremia Transmitted by Fecal Microbiota Transplant. N Engl J Med · PMID 31665575 · DOI |
Case report (two patients in two trials) |
2 Two patients who developed ESBL-producing E. coli bloodstream infection after fecal microbiota transplantation in two independent clinical trials |
Fecal microbiota transplantation No comparison group · vs No comparator |
Both infections were linked to the same stool donor by genomic sequencing. One of the patients died. The authors call for enhanced donor screening and continued vigilance about benefits and risks in different patient groups. No effect size reported (Not given) Methods, limits and fundingOutcomes: Infection linked to donor stool Limitations: Two cases; shows that serious harm can occur, not how often. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Haiyan 2025 Efficacy of probiotic intervention in unmedicated depression: a systematic review and meta-analysis. Front Psychiatry · PMID 41573044 · DOI |
Systematic review and meta analysis of randomized trials |
341 6 randomized trials of probiotic treatment in adults with depression who were not taking psychotropic medicines (169 probiotic, 172 placebo) |
Probiotic supplements Not given in the abstract · vs Placebo |
Probiotics were linked to a small reduction in depressive symptoms. When industry-funded trials or trials with add-on agents were excluded, the result was no longer significant. Only minor adverse events were reported, with no difference between groups and no serious events. SMD -0.38; after excluding industry-funded trials or add-on agents SMD -0.21 (-0.57 to -0.18; sensitivity analysis -0.65 to 0.23) Methods, limits and fundingOutcomes: Change in validated depression scales; safety Limitations: Small trial set; possible industry bias; heterogeneity (I2 51%). Funding and conflicts: The abstract reports a sensitivity analysis by funding source, which shows part of the trials were industry-funded. Registration: PROSPERO CRD420251015474 Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Hefter 2023 An 11-Year Review of Lactobacillus Bacteremia at a Pediatric Tertiary Care Center. Hosp Pediatr · PMID 37203378 · DOI |
Retrospective case review |
127845 Lactobacillus bacteremia over 11 years at a pediatric hospital (127,845 admissions) |
Hospital probiotic use 11 years · vs No comparison group |
Eight cases were found. All had signs of infection. Most had impaired intestinal function and a central venous catheter. Three had a history of probiotic use. The authors call it uncommon but say certain populations may be at higher risk. 8 cases per 127,845 admissions (Not given) Methods, limits and fundingOutcomes: Cases of Lactobacillus bloodstream infection and their risk factors Limitations: Single hospital; children; small number of cases. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Hilimire 2015 Fermented foods, neuroticism, and social anxiety: An interaction model. Psychiatry Res · PMID 25998000 · DOI |
Cross sectional survey |
710 710 young adults (445 female) who completed questionnaires |
Self-reported frequency of eating fermented foods One time point (survey) · vs Lower frequency of fermented food intake |
Fermented food intake, neuroticism and exercise each predicted social anxiety. For people high in neuroticism, more frequent fermented food intake went with fewer social anxiety symptoms. The authors say the direction of cause is unknown. Interaction between fermented food intake and neuroticism (Not given in the abstract) Methods, limits and fundingOutcomes: Social anxiety symptoms Limitations: Self-report survey at one time; cannot show that fermented foods reduced anxiety; other habits may differ between people. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Jacka 2017 A randomised controlled trial of dietary improvement for adults with major depression (the 'SMILES' trial). BMC Med · PMID 28137247 · DOI |
Randomised controlled trial (single blind) |
67 67 adults with moderate to severe depression (33 diet, 34 control); 55 were using some form of therapy; 56 had complete 12-week data |
Seven individual nutritional counselling sessions with a clinical dietitian (dietary improvement programme) 12 weeks · vs Social support sessions on the same schedule |
The diet group improved more on the MADRS than the social support group. Remission (MADRS below 10) was reached by 32.3% (10 people) of the diet group and 8.0% (2 people) of the control group. Cohen's d -1.16; number needed to treat 4.1 (NNT 95% CI 2.3 to 27.8) Methods, limits and fundingOutcomes: Montgomery-Asberg Depression Rating Scale (MADRS) at 12 weeks; remission Limitations: Small, single-site, single-blind trial; participants knew which sessions they attended; the very wide NNT interval shows the uncertainty. A large effect from a small trial needs repeating. Funding and conflicts: Funding is not stated in the abstract. Registration: ACTRN12612000251820 Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Johnson 2026 The therapeutic readiness of probiotics in major depressive disorder: A systematic review of randomised controlled trials. J Psychopharmacol · PMID 41453849 · DOI |
Systematic review of randomised trials |
13 double-blind, placebo-controlled randomised trials, 437 adults aged 18 to 75 with major depressive disorder | Probiotics (many were multi-strain Lactobacillus and Bifidobacterium products) Mostly 4 to 8 weeks · vs Placebo |
Most trials reported improvements in depressive symptoms, particularly in outpatients with mild to moderate depression using multi-strain products. Benefit was most consistent in Iranian outpatients, more modest in European inpatients and variable in East Asian outpatients. The authors describe probiotics as appearing safe and well tolerated, with modest adjunctive benefit. Not pooled (Not pooled) Methods, limits and fundingOutcomes: Depressive symptoms and secondary outcomes Limitations: Attrition, selective reporting and method differences remained sources of bias; results varied by country. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Lai 2022 Metagenomic analysis reveals gut bacterial signatures for diagnosis and treatment outcome prediction in bipolar depression. Psychiatry Res · PMID 34896845 · DOI |
Case control study with machine learning |
122 62 patients in a depressive episode of bipolar disorder and 60 healthy people |
Stool metagenomic sequencing; random forest models Patients were treated for one month with a prescription medicine · vs Healthy individuals; responders vs non-responders |
Patients showed specific alterations in gut microbial diversity and composition. Models using bacterial species separated patients from controls with an area under the curve of 0.733 and responders from non-responders with 0.800. AUC 0.733 (patients vs controls); 0.800 (responders vs non-responders) (Not given in the abstract) Methods, limits and fundingOutcomes: Microbial differences; model accuracy Limitations: Single-site, small, bipolar depression only; the abstract does not describe testing in an independent group; treatment itself changed the microbiome. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Li 2026 Adjunctive fecal microbiota transplantation for major depressive disorder: A randomized, double-blind, placebo-controlled trial. Cell Host Microbe · PMID 42309058 · DOI |
Randomized, double blind, placebo controlled trial |
Patients with major depressive disorder (number not given in the abstract) who were also receiving a standard antidepressant | Fecal microbiota transplantation capsules 2-week course; outcomes at weeks 2 and 8 · vs Placebo capsules |
Remission at week 8 did not differ significantly between groups. HAMD-17 scores fell more in the transplant group at weeks 2 and 8. Safety was comparable to placebo. The authors report donor microbes persisting and a link with bile acid changes. Remission no significant difference; HAMD-17 greater reduction at weeks 2 and 8 (Not given in the abstract) Methods, limits and fundingOutcomes: Remission rate at week 8; HAMD-17 scores; safety; microbial engraftment Limitations: One trial, in one country, with an add-on design (all took an antidepressant); sample size and funding are not in the abstract; the main outcome (remission) did not differ. Funding and conflicts: Funding is not stated in the abstract. Registration: ChiCTR2300071421 Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Liu 2019 Prebiotics and probiotics for depression and anxiety: A systematic review and meta-analysis of controlled clinical trials. Neurosci Biobehav Rev · PMID 31004628 · DOI |
Systematic review and meta analysis of controlled trials |
34 controlled clinical trials of prebiotics or probiotics for depression or anxiety, in community, medical and psychiatric samples | Probiotics or prebiotics (many products and strains) Varied by trial · vs Placebo |
Probiotics gave small effects on depression and anxiety; prebiotics did not differ from placebo. The depression effect was larger in clinical or medical samples and, in a preliminary analysis of psychiatric samples only, medium to large. The authors say there were few trials in clinical samples. Probiotics: depression d = -0.24, anxiety d = -0.10. Prebiotics: depression d = -0.08, anxiety d = 0.12. Clinical or medical samples: d = -0.45. Psychiatric samples (preliminary): d = -0.73. (Not given; p < .01 (probiotics, depression), p = .03 (probiotics, anxiety), p = .51 and p = .11 (prebiotics)) Methods, limits and fundingOutcomes: Depression and anxiety scores Limitations: Few trials in people with a diagnosis; the psychiatric-sample result was preliminary. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Masamura 2024 Differences in the human gut microbiota with varying depressive symptom severity scores. Biosci Microbiota Food Health · PMID 39364125 · DOI |
Cross sectional analysis of commercial test data |
People in Japan who used commercial gut microbiota testing services and completed a depression-tendency questionnaire (number not given in the abstract) | Commercial stool microbiome test data One time point · vs Groups by depression screening score |
No significant differences in gut microbiome composition were found among the groups. A few bacterial families (Bifidobacteriaceae, Streptococcaceae, Veillonellaceae) were candidates for differences. The authors note that participants' diagnoses were not clear. No significant composition differences (Not given in the abstract) Methods, limits and fundingOutcomes: Gut microbiome composition by depression screening score Limitations: No clinical diagnoses; screening questionnaire only; sample size not in the abstract. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Minkoff 2023 Fecal microbiota transplantation for the treatment of recurrent Clostridioides difficile (Clostridium difficile). Cochrane Database Syst Rev · PMID 37096495 · DOI |
Cochrane systematic review of randomized trials |
320 6 randomized trials of FMT for recurrent C. difficile infection in immunocompetent adults, 320 participants |
Donor-based FMT (nasoduodenal tube, enema or colonoscopy) Varied · vs Placebo, autologous FMT, no intervention or antibiotics |
FMT likely led to a large increase in resolution of the infection (moderate certainty). The review found no conclusive evidence on safety because serious events were few, and could draw no conclusions for immunocompromised people. Resolution RR 1.92; serious adverse events RR 0.73 (Resolution 1.36 to 2.71; serious adverse events 0.38 to 1.41) Methods, limits and fundingOutcomes: Resolution of infection; serious adverse events Limitations: Only 6 trials; people with severely weakened immunity were mostly excluded. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Ng 2023 Effect of Probiotic Supplementation on Gut Microbiota in Patients with Major Depressive Disorders: A Systematic Review. Nutrients · PMID 36986088 · DOI |
Systematic review (no meta analysis) |
7 clinical trials in people with major depressive disorder | Probiotic supplements Mostly 4 to 8 weeks · vs Placebo (one trial was open-label) |
Probiotics gave only modest effects on depressive symptoms. There were no consistent effects on gut microbiota diversity and, in most cases, no significant change in composition after four to eight weeks. Adverse events were not reported systematically and there were no good longer-term data. Not pooled (Not pooled) Methods, limits and fundingOutcomes: Depressive symptoms; gut microbiota diversity and composition Limitations: Small and varied set of trials; most did not control for the effect of diet on gut microbes. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Nikolova 2021 Perturbations in Gut Microbiota Composition in Psychiatric Disorders: A Review and Meta-analysis. JAMA Psychiatry · PMID 34524405 · DOI |
Systematic review and meta analysis of case control studies |
59 case-control studies of adults with depression, bipolar disorder, psychosis and schizophrenia, anorexia nervosa, anxiety, obsessive compulsive disorder, PTSD or ADHD; 34 studies (1,519 patients, 1,429 controls) in the diversity meta-analyses | Stool microbiome measures (diversity and relative abundance of gut microbes) Cross-sectional comparison · vs People without a psychiatric diagnosis |
Richness was lower in patients overall (observed species SMD -0.26; Chao1 SMD -0.5) but consistently lower only in bipolar disorder. Depleted Faecalibacterium and Coprococcus and enriched Eggerthella were shared across depression, bipolar disorder, schizophrenia and anxiety, with little specificity to one disorder. Observed species SMD -0.26; Chao1 SMD -0.5; phylogenetic diversity SMD -0.24 (Observed species -0.47 to -0.06; Chao1 -0.79 to -0.21; phylogenetic diversity -0.47 to -0.001) Methods, limits and fundingOutcomes: Alpha and beta diversity; relative abundance of gut microbes Limitations: Case-control design cannot show cause. The abstract says the confounding roles of region and medication were evaluated but does not give the result. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Porcari 2025 International consensus statement on microbiome testing in clinical practice. Lancet Gastroenterol Hepatol · PMID 39647502 · DOI |
International expert consensus statement |
International multidisciplinary expert panel | Microbiome testing in clinical practice No comparison group · vs No comparison group |
The statement says evidence supporting the clinical usefulness of microbiome diagnostics is scarce, and that commercial providers offer direct-to-consumer diagnostic tests without a consensus on regulation or any proven value in clinical practice. It sets out a framework for best practice. No effect size reported (No interval reported) Methods, limits and fundingOutcomes: Recommendations for testing; evidence for clinical usefulness Limitations: Expert consensus, not a trial; the abstract does not give the number of experts. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Rapoport 2022 Adverse events in fecal microbiota transplantation: a systematic review and meta-analysis. Ann Gastroenterol · PMID 35479587 · DOI |
Systematic review and meta analysis |
5099 61 studies of FMT for recurrent Clostridioides difficile infection, 5,099 patients |
Fecal microbiota transplantation Varied · vs Not pooled against a control |
Serious adverse events related to FMT occurred in less than 1% of patients; serious events not related to FMT were 2.9%. Minor adverse events were infrequent, self-limited gut and body discomfort. SAEs related to FMT below 1%; unrelated 2.9% (Not given in the abstract) Methods, limits and fundingOutcomes: Serious adverse events Limitations: Includes mostly uncontrolled studies in a specific infection; says little about use for depression. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Ribera 2024 Probiotic, prebiotic, synbiotic and fermented food supplementation in psychiatric disorders: A systematic review of clinical trials. Neurosci Biobehav Rev · PMID 38280441 · DOI |
Systematic review of clinical trials |
47 articles from 42 studies in people with a psychiatric diagnosis (major depression 19 studies, schizophrenia 11, bipolar disorder 5, generalized anxiety disorder 1 and others) | Probiotics, prebiotics, synbiotics or fermented foods Varied · vs Placebo or usual care (varied) |
Except in major depression, current evidence does not clarify the role of probiotics and prebiotics in treating mental illness. Several studies pointed to improvement in markers such as CRP and IL-6. Not pooled (Not pooled) Methods, limits and fundingOutcomes: Psychiatric symptoms and inflammatory markers Limitations: Only one study in generalized anxiety disorder; lifestyle and diet were possible confounders. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Servetas 2026 Evaluating the analytical performance of direct-to-consumer gut microbiome testing services. Commun Biol · PMID 41748906 · DOI |
Laboratory evaluation (method comparison) |
7 Seven direct-to-consumer gut microbiome testing services tested with a standardized NIST-developed human fecal material |
Direct-to-consumer stool test services Single evaluation · vs The standard material and between-provider comparison |
The tests showed major discrepancies within and across providers. Variability between providers was on the same scale as biological variability between donors. The authors attribute this to methodological variability and lack of quality control. Between-provider variability similar in size to between-donor variability (Not given) Methods, limits and fundingOutcomes: Analytical performance (do tests agree?) Limitations: Tested standard material, not people; only seven services. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Simpson 2021 The gut microbiota in anxiety and depression - A systematic review. Clin Psychol Rev · PMID 33271426 · DOI |
Systematic review |
26 studies: 2 case-control comparisons in generalised anxiety disorder, 18 in depression, 1 in both, 5 symptom-only | Gut microbiota comparisons Cross-sectional · vs People without the condition |
Alpha and beta diversity findings were inconsistent. Differences in taxa pointed to more pro-inflammatory species (for example Enterobacteriaceae and Desulfovibrio) and fewer short-chain fatty acid producers (for example Faecalibacterium). The authors say future research should assess confounders, particularly diet and psychotropic medicines. Not given (Not given) Methods, limits and fundingOutcomes: Diversity and bacterial taxa in anxiety and depression Limitations: Only 2 case-control studies in generalised anxiety disorder; diet and medicines not well controlled. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Valles-Colomer 2019 The neuroactive potential of the human gut microbiota in quality of life and depression. Nat Microbiol · PMID 30718848 · DOI |
Population cohort with validation cohorts |
1054 Flemish Gut Flora Project (1,054 people) with validation in independent data sets (1,070 in total) |
Stool metagenomes and questionnaires on quality of life and depression Cross-sectional · vs Comparison across people |
Butyrate-producing Faecalibacterium and Coprococcus were associated with higher quality of life. Coprococcus and Dialister were also depleted in depression, even after correcting for antidepressants. Not given as one number in the abstract (Not given in the abstract) Methods, limits and fundingOutcomes: Gut microbial features linked with quality of life and depression Limitations: A link, not proof of cause. The authors themselves stress the importance of confounders. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Wang 2026 Case Series of Bacteremia Associated with Probiotic Use in Children after Cardiac Surgery, China. Emerg Infect Dis · PMID 41612523 · DOI |
Case series within a hospital cohort |
16436 16,436 children who had cardiac surgery in China (2019 to 2024); 5,034 received probiotics |
Perioperative probiotics No comparison group · vs No comparison group |
Six children developed bloodstream infection with probiotic strains (Bacillus subtilis, Bacillus licheniformis, Lacticaseibacillus rhamnosus). Three of them had not received probiotics directly, suggesting cross-contamination or catheter-related spread. All six had complex congenital heart disease and central venous catheters. Antibiotics cleared the blood cultures in all; one child died of the underlying heart disease. 6 cases among 5,034 children given probiotics (probiotic-strain bacteremia) (Not given) Methods, limits and fundingOutcomes: Bacteremia with probiotic strains Limitations: Observational, a very specific group of severely ill children; the authors say the infection is rare. Funding and conflicts: Funding is not stated in the abstract. Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| Zhang 2025 Clinical efficacy of fecal microbiota transplantation in alleviating depressive symptoms: a meta-analysis of randomized trials. Front Psychiatry · PMID 41122746 · DOI |
Systematic review and meta analysis of randomized trials |
681 12 randomized trials with 681 participants, including people with irritable bowel syndrome and people with neurological or psychiatric conditions |
Fecal microbiota transplantation (capsule, endoscopic or enema routes) Effects short to mid term; diminished by 6 months · vs Control conditions |
FMT reduced depressive symptoms overall. Direct delivery into the gut looked stronger than capsules. Benefits were most notable in the short to mid term and diminished by 6 months. The effect was stronger in people with irritable bowel syndrome (SMD -1.06) than in people with neurological or psychiatric conditions (SMD -0.67). SMD -1.21; sensitivity analysis SMD -0.56; IBS -1.06; neurological or psychiatric -0.67; I2 47% (-1.87 to -0.55; sensitivity -0.86 to -0.26) Methods, limits and fundingOutcomes: Depressive symptoms Limitations: Mixed populations (many with gut disease, not depression); different procedures; effects faded by 6 months; small trials. Funding and conflicts: Funding is not stated in the abstract. Registration: PROSPERO CRD42025638185 Read: Abstract read through PubMed (esummary and efetch) on 2026-10-31; full text not read. |
| p23759244 Psychobiotics: a novel class of psychotropic. (Biol Psychiatry 2013) · Source |
Narrative review human and animal |
Methods, limits and fundingRead: abstract | ||
| p27793434 Psychobiotics and the Manipulation of Bacteria-Gut-Brain Signals. (Trends Neurosci 2016) · Source |
Narrative review human and animal |
Methods, limits and fundingRead: abstract | ||
| p31460832 The Microbiota-Gut-Brain Axis. (Physiol Rev 2019) · Source |
Narrative review human and animal |
Methods, limits and fundingRead: abstract | ||
| p31978342 Establishing or Exaggerating Causality for the Gut Microbiome: Lessons from Human Microbiota-Associated Rodents. (Cell 2020) · Source |
Systematic review of animal studies animal studies reviewed |
Methods, limits and fundingRead: abstract | ||
| s-fda-vowst FDA: VOWST (content current as of 05/18/2023) · Source |
Regulator n/a |
Methods, limits and fundingRead: full-text | ||
| s-nccih-probiotics NCCIH: Probiotics: Usefulness and Safety (Last Updated August 2019) · Source |
Health agency n/a |
Methods, limits and fundingRead: full-text | ||
| s-nimh-depression NIMH: Depression · Source |
Health agency n/a |
Methods, limits and fundingRead: full-text | ||
| s-nimh-help NIMH: Help for Mental Illnesses · Source |
Health agency n/a |
Methods, limits and fundingRead: full-text |
What we do not know yet
- No trial read tested one named probiotic strain against placebo in a large, independent, long-term study in people with a diagnosed anxiety disorder.
- No review read compared probiotic trials by strain with enough trials per strain to say which strains work.
- Trials are short (mostly up to 8 weeks); no long-term follow-up was read.
- Only one randomized FMT trial in major depression was read, and its main outcome (remission) did not differ.
- No validated stool test for depression or anxiety was found.
- Safety data for probiotics in pregnancy and breastfeeding were not read.
How new research is added
New studies are found by a saved PubMed search and placed in a review queue before the page changes.
Lab markers
What changed in blood or saliva tests during trials. A changed number is not the same as feeling or being healthier, and we give no "normal ranges".
Other 6
Gut microbe composition (stool microbiome)
Group differences, not consistent: often fewer butyrate-producing bacteria (Faecalibacterium, Coprococcus) and more of some pro-inflammatory groups (such as Eggerthella); diversity results conflicted. in trials
The mix and variety of microbes found in a stool sample, usually measured by gene sequencing.
Mixed findingsResults and what it means
Why it was measured
To see whether people with depression or anxiety have different gut microbes from people without.
Statistical vs. clinical meaning
These are group averages seen at one moment. They do not show that microbes cause low mood, and they cannot be used to diagnose an individual.
| Study | Result | People | Product |
|---|---|---|---|
| 18 | Depleted Faecalibacterium and Coprococcus and enriched Eggerthella shared across diagnoses; richness lower overall but consistent only in bipolar disorder | 59 case-control studies; 1,519 patients and 1,429 controls in diversity analyses | Stool microbiome comparison |
| 24 | Coprococcus and Dialister depleted in depression, also after correcting for antidepressants | 1,054 people with validation in independent data sets | Stool metagenomes |
| 23 | Diversity inconsistent; more pro-inflammatory and fewer short-chain fatty acid producing bacteria | 26 studies, mostly depression | Stool microbiome comparison |
| 4 | Diversity inconsistent; conflicting taxa results because of diet and medicine confounders | 24 articles, 20 from China | Stool microbiome comparison |
Depression symptom scores
Lower scores with probiotics and diet support in several trials, with large differences between reviews. in trials
Rating scales (for example MADRS) that score how severe depressive symptoms are.
Low certaintyResults and what it means
Why it was measured
The main outcome in trials of probiotics and diet.
Statistical vs. clinical meaning
Scale scores matter to patients but self-reported scales can be affected by knowing which treatment you receive, and the trials were short.
| Study | Result | People | Product |
|---|---|---|---|
| 14 | Probiotics d -0.24 vs placebo; prebiotics no difference | 34 controlled trials | Probiotics or prebiotics |
| 1 | Probiotics SMD -0.96 | 23 trials, 1,401 patients | Probiotics |
| 7 | Probiotic monotherapy SMD -0.38; not significant after excluding industry-funded trials | 6 trials, 341 adults | Probiotics |
| 10 | MADRS fell more with dietary support (d -1.16) | 67 adults | Dietitian-led diet support |
Anxiety symptom scores
Small to moderate reductions with probiotics in two meta-analyses. in trials
Rating scales that score how severe anxiety symptoms are.
Very low certaintyResults and what it means
Why it was measured
A secondary outcome in many trials of probiotics.
Statistical vs. clinical meaning
Anxiety was a side outcome in trials built around depression.
Perceived stress score
Fell in both diet groups; the psychobiotic diet did not differ significantly from control. in trials
A questionnaire score of how stressed a person feels.
Not enough evidenceResults and what it means
Remission and HAMD-17 depression score
No significant remission difference at week 8; greater HAMD-17 reduction at weeks 2 and 8 with FMT. in trials
Remission is a score below a set cut-off; HAMD-17 is a clinician-rated depression scale.
Not enough evidenceResults and what it means
Why it was measured
Clinical outcomes in the FMT trial.
Statistical vs. clinical meaning
One trial, add-on design, null main outcome.
| Study | Result | People | Product |
|---|---|---|---|
| 13 | Remission not significantly different; HAMD-17 fell more with FMT | Patients with major depressive disorder taking an antidepressant | FMT capsules vs placebo |
Accuracy of microbiome-based classifiers (AUC)
Moderate accuracy in one research study; not tested in independent groups in the sources read. in trials
AUC measures how well a model separates two groups; 0.5 is a coin flip and 1.0 is perfect.
Very low certaintyResults and what it means
Why it was measured
To judge whether a stool test could diagnose or predict treatment response.
Statistical vs. clinical meaning
A modest AUC in one study does not make a usable clinical test.
| Study | Result | People | Product |
|---|---|---|---|
| 12 | AUC 0.733 patients vs controls; 0.800 responders vs non-responders | 62 patients with bipolar depression, 60 controls | Random forest on stool metagenomes |
Safety
What studies and official sources say about side effects, medicines and who should check first. Each point shows what kind of evidence it comes from.
Main points to know 5
- This is not a replacement for mental health care. Persistent low mood, anxiety, thoughts of self-harm, or big changes in sleep or appetite need assessment by a health professional. NIMH describes depression as an illness with severe symptoms that affect how you feel, think and handle daily activities, and says treatment usually includes therapy, medication, or both. NCCIH says not to use probiotics as a reason to postpone seeing your health care provider about any health problem and to consult one first if you have health problems. Do not stop, reduce or replace prescribed medicines for a probiotic, diet or test result without talking to the prescriber. (The advice not to change medicines without the prescriber is general safety guidance, not a quoted source.) Health agency guidance 33 34 32
- If you are thinking about harming yourself, get help now. If you are thinking about ending your life, or you cannot keep yourself safe, contact your local emergency services or a crisis line in your country right away, or go to the nearest emergency department, and tell someone you trust. Microbiome products and tests are not a treatment for a mental health crisis. NIMH says that in the United States, in life-threatening situations you call 911, and that anyone struggling or having thoughts of suicide can call or text 988 (Suicide & Crisis Lifeline). Elsewhere, use your local emergency number or national crisis service. Health agency guidance 34 33
- Probiotics can cause serious infections in people who are very ill or have weakened immunity. NCCIH says probiotics have an extensive history of apparently safe use, particularly in healthy people, but the risk of harmful effects is greater in people with severe illnesses or compromised immune systems. Cases of severe or fatal infections have been reported in premature infants, and the FDA has warned health care providers about this. In a Chinese cohort of 16,436 children after heart surgery, six developed bloodstream infection with probiotic strains, and all six had central venous catheters; in an 11-year review at one children's hospital there were 8 Lactobacillus bloodstream infections among 127,845 admissions, most in patients with impaired gut function and a central line. People with weakened immune systems, a central line, a serious illness or a premature baby should only use probiotics if their clinician decides it is right. Health agency guidance and case series 32 25 8
- Fecal microbiota transplant is a medical procedure with real risks. FMT is used by clinicians for recurrent Clostridioides difficile infection. In a Cochrane review of 6 trials (320 adults) it likely led to a large increase in resolution of that infection, but the review found no conclusive evidence on safety. In two clinical trials, two patients developed drug-resistant E. coli bloodstream infection linked to the same stool donor, and one of them died. A pooled analysis in C. difficile patients found serious events related to FMT in less than 1%. The FDA page for VOWST lists its indication as preventing recurrence of C. difficile infection in adults after antibacterial treatment, not depression. Do-it-yourself transplants are not safe and have no place here. Systematic reviews, case report and regulator page 16 6 20 31
- Consumer microbiome tests cannot diagnose depression or anxiety. An international expert panel says commercial microbiome diagnostic tests are offered without consensus on regulation or any proven value in clinical practice. A test of seven services using the same standard stool material found major discrepancies within and across providers, as large as the biological differences between donors. A result may also lead to unneeded supplements, diets or worry, or to false reassurance and delay in seeking care. Expert consensus and laboratory comparison 19 22 15
Side effects 7
| Effect | How often | Severity and recovery | Evidence |
|---|---|---|---|
| Bloodstream infection with probiotic bacteria or yeast Risk groups named: central venous catheter, impaired gut function, premature infants, weakened immunity (NCCIH). | 6 cases among 5,034 children given probiotics after heart surgery; 8 Lactobacillus cases in 127,845 pediatric admissions over 11 years | Serious (fever, systemic infection); treated with antibiotics in the series read Cleared with antibiotics in all six children in the heart-surgery series; one child died from the underlying heart disease | Case series 25 8 |
| Severe or fatal infection in premature infants given probiotics NCCIH says the FDA warned health care providers about this risk. | Frequency not given on the page | Severe, potentially fatal Not stated | Health agency guidance 32 |
| Other possible harms of probiotics: harmful substances produced by the organisms and transfer of antibiotic resistance genes NCCIH says few studies have looked at the safety of probiotics in detail, so the frequency and severity of side effects is not well known. | Not stated | Not stated Not stated | Health agency guidance 32 |
| Minor side effects in probiotic trials A 2023 review found adverse events were not reported systematically in the depression trials. | No difference from placebo in a 6-trial analysis | Minor Not stated | Systematic review of randomized trials 7 17 |
| Bloodstream infection from a drug-resistant bacterium carried in donor stool (FMT) The authors call for stronger donor screening. | Two cases reported linked to one donor | Serious; one death Not stated | Case report 6 |
| Minor gut and body discomfort after FMT Serious events related to FMT in this infection were below 1%; this does not apply automatically to people using FMT for depression. | Infrequent in a pooled analysis of 5,099 patients with C. difficile infection | Minor, self-limited Self-limited | Systematic review and meta analysis 20 |
| Product contents not matching the label NCCIH says some probiotic products have been reported to contain microorganisms other than those listed on the label. | Not stated | Some contaminants may pose serious health risks Not stated | Health agency guidance 32 |
Medicines and supplements 3
| With | Why it matters | Importance | Evidence | What to do |
|---|---|---|---|---|
| Psychiatric medicines and antidepressants prescription | No interaction study with probiotics, prebiotics or diets was read. The 2026 FMT trial gave FMT capsules alongside a standard antidepressant and reported tolerability comparable to placebo. | No interaction between probiotics and psychiatric medicines was found in the sources read. Absence of a study is not proof of safety. | Absence of evidence Not enough evidence 13 | Tell your prescriber about any probiotic, supplement or diet change, and do not change a prescribed medicine on your own. |
| Medicines that weaken the immune system, chemotherapy and other immune suppression prescription | NCCIH says the risk of harmful effects from probiotics is greater in people with severe illnesses or compromised immune systems. | Live bacteria or yeast in a probiotic may cause infection when immunity is weak. | Health agency guidance Moderate certainty 32 | Ask the clinician who treats you before taking any probiotic if your immune system is weakened. |
| Antibiotics prescription | NCCIH lists transfer of antibiotic resistance genes from probiotic organisms to other gut microbes as a possible harm; the part read gives no rule on timing with antibiotics. | No source read gives guidance on combining probiotics with antibiotics for mood. | Absence of evidence Not enough evidence 32 | Ask a doctor or pharmacist. |
Who should check first 5
| Situation | Advice | Evidence |
|---|---|---|
| Weakened immune system, serious illness, a central venous catheter or recent major surgery | Ask the treating clinician before using any probiotic. NCCIH says the risk of harm is greater in these groups. | Health agency guidance and case series 32 25 8 |
| Premature infants | Not for self-treatment. NCCIH says severe or fatal infections have been reported and the FDA has warned health care providers. | Health agency guidance 32 |
| Thoughts of self-harm, severe depression or a mental health crisis | Seek urgent professional help. A microbiome product or test is not a treatment for a crisis. | Health agency guidance 34 |
| Fecal transplant outside a clinical setting | Do not try it yourself. In two trials donor stool carried a drug-resistant bacterium and one patient died. | Case report 6 |
| Planning to stop or replace a prescribed treatment because of a probiotic, diet or test result | Talk to the prescriber first (general safety guidance). | General safety guidance |
Overdose, product quality and regulators
| Body | Action | Date |
|---|---|---|
| National Center for Complementary and Integrative Health (NCCIH, US) (United States) | Probiotics page: in most instances we still do not know which probiotics are helpful and which are not; risk of harm is greater in people with severe illness or weakened immunity; severe or fatal infections reported in premature infants and the FDA warned providers; do not use probiotics as a reason to postpone seeing a provider; probiotic supplements do not need FDA approval before they are marketed. source | 2019-08 |
| US Food and Drug Administration (United States) | VOWST (fecal microbiota spores, live-brpk) is indicated to prevent recurrence of Clostridioides difficile infection in adults after antibacterial treatment for recurrent infection. It is not listed for depression or any mental health condition. source | 2023-05-18 |
| National Institute of Mental Health (NIMH, US) (United States) | Help page: in life-threatening situations call 911; if suicidal or in emotional distress consider the 988 Suicide & Crisis Lifeline by call, text or chat; a primary care provider can do an initial mental health screening and refer. source | Not dated on the page |
When to get medical help
- Thoughts of harming yourself or ending your life, or feeling you cannot keep yourself safe: contact local emergency services or a crisis line in your country right away, or go to the nearest emergency department, and tell someone you trust. In the US, NIMH lists 911 for emergencies and 988 (call or text) for crisis support.
- Fever, chills, a fast heartbeat, confusion or feeling very unwell after starting a probiotic or after a fecal transplant, especially with a weakened immune system, a central line or a serious illness: seek urgent medical help. Fever was common in the case series read; the rest of this wording is general guidance.
- Low mood, anxiety, loss of interest or changes in sleep or appetite that last more than a couple of weeks or get in the way of daily life: see a doctor or mental health professional (general guidance, consistent with NIMH).
- Severe or bloody diarrhea, severe abdominal pain or persistent vomiting after a probiotic or FMT: contact a clinician promptly (general safety guidance, not a quoted source).
Stop using the product and contact a clinician or emergency service. In the US, Poison Control is 1-800-222-1222.
General information only, not medical advice. Ask a clinician or pharmacist before use, especially with medicines, in pregnancy or with a health condition. See the Natural Remedy Safety guide.
Frequently asked questions
Does gut bacteria cause depression?
What is the gut-brain axis?
A 2019 review describes two-way communication between gut microbes and the brain through the immune system, tryptophan metabolism, the vagus nerve and the gut nervous system. Much of the detail comes from animals.
Do probiotics help depression?
Do probiotics help anxiety?
What are psychobiotics?
Do prebiotics or fibre help mood?
Does a Mediterranean-style diet help depression?
Do fermented foods help anxiety or stress?
Is a fecal transplant a treatment for depression?
Can a gut microbiome test tell me if I am depressed or anxious?
Who should avoid probiotics or ask a doctor first?
Explore by health goal
Editorial transparency
- Written by
- AlternativeMed editorial team. Research compiled with AI assistance, then checked against PubMed records.
- Medical review
- None. This page has not been reviewed by a physician or pharmacist.
- First published
- 2026-10-31
- Last substantive update
- 2026-10-31
- How we research
- We searched PubMed, read the abstract of every review, trial and study cited, and read the NCCIH, FDA and NIMH pages as downloaded text. Full texts were not read. Certainty ratings are the compiler's own reading unless a review gives its own grade (stated in the text). Funding is not stated in most abstracts, and this is noted where relevant.
- How we rate evidence
- See "How we rate evidence" in the Evidence tab.
- Independence
- No product is promoted on this page. No affiliate links are shown.
Sources 34
Each source was opened and checked. Where we read only the abstract, it says so. The small numbers in the text point here.
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- . Psychobiotics: a novel class of psychotropic. (Biol Psychiatry 2013). . . (abstract)
- . Psychobiotics and the Manipulation of Bacteria-Gut-Brain Signals. (Trends Neurosci 2016). . . (abstract)
- . The Microbiota-Gut-Brain Axis. (Physiol Rev 2019). . . (abstract)
- . Establishing or Exaggerating Causality for the Gut Microbiome: Lessons from Human Microbiota-Associated Rodents. (Cell 2020). . . (abstract)
- . FDA: VOWST (content current as of 05/18/2023). . . (full-text)
- . NCCIH: Probiotics: Usefulness and Safety (Last Updated August 2019). . . (full-text)
- . NIMH: Depression. . . (full-text)
- . NIMH: Help for Mental Illnesses. . . (full-text)