4.5 Article

Effects of Psychotropics on the Microbiome in Patients With Depression and Anxiety: Considerations in a Naturalistic Clinical Setting

Journal

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/ijnp/pyaa070

Keywords

anxiety; depression; microbial diversity; microbiome; psychotropics

Funding

  1. Japan Society for the promotion of science KAKENHI [18H04805]
  2. Japan Science and Technology Agency Precursory Research for Embryonic Science and Technology [JPMJPR1537]
  3. Japan Agency for Medical Research and Development Core Research for Evolutional Science and Technology [JP19gm1010009]
  4. Japan Science and Technology Agency Exploratory Research for Advanced Technology [JPMJER1902]
  5. Takeda Science Foundation
  6. Food Science Institute Foundation
  7. Program for the Advancement of Research in Core Projects under Keio University's Longevity Initiative
  8. Japan Dairy Association J-milk

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This longitudinal study investigated the relationship between prescribed medications and gut bacterial diversity in patients with major depressive disorders and anxiety disorders. The results showed that antipsychotics may decrease the alpha diversity of the gut microbiome among patients with depression and anxiety, with a relationship to medication dosage. Further research is needed to elucidate the mechanisms of gut-brain interactions in psychiatric disorders.
Background: The antibacterial effects of psychotropics may be part of their pharmacological effects when treating depression. However, limited studies have focused on gut microbiota in relation to prescribed medication. Method: We longitudinally investigated the relationship between patients' prescribed medications and intestinal bacterial diversity in a naturalistic treatment course for patients with major depressive disorders and anxiety disorders. Patients were recruited and their stool was collected at 3 time points during their usual psychiatric treatments. Gut microbiota were analyzed using 16S rRNA gene sequencing. We examined the impact of psychotropics (i.e., antidepressants, anxiolytics, antipsychotics) on their gut microbial diversity and functions. Results: We collected 246 stool samples from 40 patients. Despite no differences in microbial diversity between medication groups at the baseline, over the course of treatment, phylogenic diversity whole-tree diversity decreased in patients on antipsychotics compared with patients without (P=.027), and beta diversity followed this trend. Based on a fixed-effect model, antipsychotics predicted microbial diversity; the higher doses correlated with less diversity based on the Shannon index and phylogenic diversity whole tree (estimate = -0.00254, SE= 0.000595, P< .0001; estimate = -0.02644, SE =0.00833, P = .002, respectively). Conclusion: Antipsychotics may play a role in decreasing the alpha diversity of the gut microbiome among patients with depression and anxiety, and our results indicate a relationship with medication dosage. Future studies are warranted and should consider patients' types and doses of antipsychotics in order to further elucidate the mechanisms of gut-brain interactions in psychiatric disorders.

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