Pharmacomicrobiomics of Antidepressants in Depression: A Systematic Review

Author:

Brown Lisa C.1ORCID,Bobo William V.2,Gall Cory A.3,Müller Daniel J.456,Bousman Chad A.789ORCID

Affiliation:

1. Great Scott! Consulting LLC, New York, NY 11222, USA

2. Department of Psychiatry & Psychology, Mayo Clinic, Jacksonville, FL 32224, USA

3. Department of Veterinary Tropical Diseases, University of Pretoria, Onderstepoort 0028, South Africa

4. Pharmacogenetics Research Clinic, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, ON M6J 1H4, Canada

5. Department of Psychiatry, University of Toronto, Toronto, ON M6J 1H4, Canada

6. Department of Psychiatry, Psychosomatics and Psychotherapy, Center of Mental Health, University Hospital of Würzburg, 97080 Würzburg, Germany

7. The Mathison Centre for Mental Health Research and Education, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 4N1, Canada

8. Departments of Medical Genetics, Psychiatry, Physiology and Pharmacology, and Community Health Sciences, University of Calgary, Calgary, AB T2N 4N1, Canada

9. Alberta Children’s Hospital Research Institute, University of Calgary, Calgary, AB T2N 4N1, Canada

Abstract

This systematic review evaluated the animal and human evidence for pharmacomicrobiomics (PMx) interactions of antidepressant medications. Studies of gut microbiota effects on functional and behavioral effects of antidepressants in human and animal models were identified from PubMed up to December 2022. Risk of bias was assessed, and results are presented as a systematic review following PRISMA guidelines. A total of 28 (21 animal, 7 human) studies were included in the review. The reviewed papers converged on three themes: (1) Antidepressants can alter the composition and metabolites of gut microbiota, (2) gut microbiota can alter the bioavailability of certain antidepressants, and (3) gut microbiota may modulate the clinical or modeled mood modifying effects of antidepressants. The majority (n = 22) of studies had at least moderate levels of bias present. While strong evidence is still lacking to understand the clinical role of antidepressant PMx in human health, there is evidence for interactions among antidepressants, microbiota changes, microbiota metabolite changes, and behavior. Well-controlled studies of the mediating and moderating effects of baseline and treatment-emergent changes in microbiota on therapeutic and adverse responses to antidepressants are needed to better establish a potential role of PMx in personalizing antidepressant treatment selection and response prediction.

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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