The DOI matches its Crossref record; 49 of the 49 references it cites were found in a registry or an index.
Current Perspectives on Gut Microbiome Dysbiosis and Depression
Open accessAbstract
The human gut microbiome partakes in a bidirectional communication pathway with the central nervous system (CNS), named the microbiota-gut-brain axis. The microbiota-gut-brain axis is believed to modulate various central processes through the vagus nerve as well as production of microbial metabolites and immune mediators which trigger changes in neurotransmission, neuroinflammation, and behavior. Little is understood about the utilization of microbiome manipulation to treat disease. Though studies exploring the role of the microbiome in various disease processes have shown promise, mechanisms remain unclear and evidence-based treatments for most illnesses have not yet been developed. The animal studies reviewed here offer an excellent array of basic science research that continues to clarify mechanisms by which the microbiome may affect mental health. More evidence is needed, particularly as it relates to translating this work to human subjects. The studies presented in this paper largely demonstrate encouraging results in the treatment of depression. Limitations include small sample sizes and heterogeneous methodology. The exact mechanism by which the gut microbiota causes or alters neuropsychiatric disease states is not fully understood. In this review, we focus on recent studies investigating the relationship between gut microbiome dysbiosis and the pathogenesis of depression. This article is based on previously conducted studies and does not contain any studies with human participants or animals performed by any of the authors.
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“The participation of gut microbiome in bidirectional communication pathway with the central nervous system (CNS) was named the microbiota-gut-brain axis, which is believed to regulate various central processes through microbial metabolites [98].”
From Circular RNAs in depression: Biogenesis, function, expression, and therapeutic potential (2021) · cites this paper as [98]
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Citations
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“…and X-17,325 are all unidentified compounds and do not have relevant chemical identifiers (HMDB, KEGG ID, PubChem) abundances of Bifidobacterium, Ruminococcus, and Esch - erichia/Shigella in patients with severe depression (Cheung et al. 2019; Capuco et al. 2020), aligning with our finding.”
Fatigue, depressive symptoms, and stress relate to diet quality and food Choices
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Metadata
- Authors
- Capuco, A., Urits, I., Hasoon, J., Chun, R., Gerald, B., Wang, J. K., Kassem, H., Ngo, A. L., Abd-Elsayed, A., Simopoulos, T., Kaye, A. D., & Viswanath, O.
- Affiliations
- Georgetown University (US)
- Beth Israel Deaconess Medical Center (US)
- University of Arizona College of Medicine- Phoenix (US)
- Harvard University (US)
- Mount Sinai Medical Center (US)
- University of Wisconsin–Madison (US)
- Louisiana State University Health Sciences Center Shreveport (US)
- Creighton University (US)
- Corresponding author
- Urits, Ivan
- ORCID
- Venue
- Advances in Therapy
- Published
- 2020-03-04
- Volume
- 37
- Issue
- 4
- Pages
- 1328-1346
- ISSN
- 0741-238X (ISSN-L)
- 1865-8652
- PMC
- PMC7140737
- OpenAlex
- W3010636850
- Cited by
- 216
- References
- 49
- Citations by year
- 2026: 18 · 2025: 29 · 2024: 33 · 2023: 59 · 2022: 41 · 2021: 27 · 2020: 7
- FWCI
- 3.21
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Advances in Therapy (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Keywords
- gut dysbiosis, depression, microbiota-gut-brain axis, vagus nerve, microbial metabolites, neuroinflammation, neurotransmission, neuropsychiatric disorders, animal models of depression, microbiota-based therapy
- MeSH terms
- Gastrointestinal Microbiome, Animals, Brain, Central Nervous System, Depression, Humans, Dysbiosis
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