Evidence map›Paper›PMID 39794490›Full record

ArticleMolecular psychiatry2025

Medication use is associated with distinct microbial features in anxiety and depression.

Amanda Hazel Dilmore, Rayus Kuplicki, Daniel McDonald, Megha Kumar, Mehrbod Estaki, Nicholas Youngblut, Alexander Tyakht, Gail Ackermann, Colette Blach, Siamak MahmoudianDehkordi and 9 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors.

Amanda Hazel DilmoreDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.ORCID http://orcid.org/0000-0001-6493-7116
Rayus KuplickiLaureate Institute for Brain Research, Tulsa, OK, USA.ORCID http://orcid.org/0000-0003-2954-6421
Daniel McDonaldDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Megha KumarDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Mehrbod EstakiDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Nicholas YoungblutDepartment of Microbiome Science, Max Planck Institute for Biology, Tübingen, Germany.
Alexander TyakhtDepartment of Microbiome Science, Max Planck Institute for Biology, Tübingen, Germany.
Gail AckermannDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA.
Colette BlachDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, USA.
Siamak MahmoudianDehkordiDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, USA.
Boadie W DunlopDepartment of Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.ORCID http://orcid.org/0000-0002-4653-0483
Sudeepa BhattacharyyaDepartment of Biological Sciences, Arkansas Biosciences Institute, Arkansas State University, Jonesboro, AR, USA.
Salvador GuinjoanLaureate Institute for Brain Research, Tulsa, OK, USA.ORCID http://orcid.org/0000-0002-1958-4259
Pooja MandaviyaDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands.ORCID http://orcid.org/0000-0002-7730-4462
Ruth E LeyDepartment of Microbiome Science, Max Planck Institute for Biology, Tübingen, Germany.
Rima Kaddaruh-DauokDepartment of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, USA.ORCID http://orcid.org/0000-0003-1858-5732
Martin P PaulusLaureate Institute for Brain Research, Tulsa, OK, USA.ORCID http://orcid.org/0000-0002-0825-3606
Rob KnightDepartment of Pediatrics, University of California San Diego, La Jolla, CA, USA. rknight@health.ucsd.edu.
Alzheimer Gut Microbiome Project Consortium

Funding

Project 4 - Mechanistic studies on the role of the gut microbiome in models for Alzheimer's diseaseU19AG063744 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI Rima F Kaddurah-Daouk · 2019 to 2026
$54.1M
Metabolomic Signatures for Disease Sub-classification and Target Prioritization in AMP-ADU01AG061359 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, KASTENMULLER, GABI · 2018 to 2022
$10.0M
Metabolic Signatures Underlying Vascular Risk Factors for Alzheimer-type DementiasRF1AG051550 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, KLING, MITCHEL ALLAN · 2015 to 2016
$6.3M
Metabolic Networks and Pathways Predictive of Sex Differences in AD Risk and Responsiveness to TreatmentRF1AG059093 · NIA · DUKE UNIVERSITY · PI BRINTON, ROBERTA EILEEN, CHANG, RUI · 2018 to 2018
$5.9M
Metabolic Networks and Pathways in Alzheimer's DiseaseR01AG046171 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F · 2014 to 2017
$4.4M
Metabolic Network Analysis of Biochemical Trajectories in Alzheimer's DiseaseRF1AG057452 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, KASTENMULLER, GABI · 2017 to 2017
$3.5M
Gut Liver Brain Biochemical Axis in Alzheimer's DiseaseRF1AG058942 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, VAN DUIJN, CORNELIA MARJA · 2018 to 2018
$3.4M
NIA NIH HHS R01 AG046171NIA NIH HHS RF1 AG051550NIA NIH HHS RF1 AG057452NIA NIH HHS RF1 AG058942NIA NIH HHS RF1 AG059093NIA NIH HHS U01 AG061359NIA NIH HHS U19 AG063744U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) 5U19AG063744U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) U19AG063744
6 · The paper itself

Abstract

This study investigated the relationship between gut microbiota and neuropsychiatric disorders (NPDs), specifically anxiety disorder (ANXD) and/or major depressive disorder (MDD), as defined by Diagnostic and Statistical Manual of Mental Disorders (DSM)-IV or V criteria. The study also examined the influence of medication use, particularly antidepressants and/or anxiolytics, classified through the Anatomical Therapeutic Chemical (ATC) Classification System, on the gut microbiota. Both 16S rRNA gene amplicon sequencing (16S) and shallow shotgun sequencing (WGS) were performed on DNA extracted from 666 fecal samples from the Tulsa-1000 and Neurocomputational Mechanisms of Affiliation and Personality Study Center for Biomedical Research Excellence (NeuroMAP CoBRE) cohorts. The results highlight the significant influence of medication use; antidepressant use is associated with significant differences in gut microbiota beta diversity and has a larger effect size than NPD diagnosis. Next, specific microbes were associated with ANXD and MDD, highlighting their potential for non-pharmacological intervention. Finally, the study demonstrated the capability of Random Forest classifiers to predict diagnoses of NPD and medication use from microbial profiles, suggesting a promising direction for the use of gut microbiota as biomarkers for NPD. Though the effect sizes were larger in females than males, similar trends emerged for both sexes. These findings encourage future research on the gut microbiota's role in NPD and its interactions with pharmacological treatments.

Indexed as

AnxietyAnxiety DisordersGastrointestinal MicrobiomeAdultAnti-Anxiety AgentsAntidepressive AgentsDepressionFecesFemaleHumansMajor Depressive DisorderMaleMiddle AgedRNA, Ribosomal, 16SAnti-Anxiety AgentsAntidepressive AgentsRNA, Ribosomal, 16S

Identifiers

PMID39794490
PMCPMC12092254

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.