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Association Between Gut Microbiota and Depressive Symptoms: A Cross-Sectional Population-Based Study in South Korea

Title
Association Between Gut Microbiota and Depressive Symptoms: A Cross-Sectional Population-Based Study in South Korea
Authors
Kim, Sun-YoungPark, EunkyoLim, Weon-JeongKim, Soo InJeon, Sang WonChang, YoosooRyu, SeunghoKim, Hyung-LaeKim, Han-Na
Ewha Authors
김형래임원정김수인김선영
SCOPUS Author ID
김형래scopusscopusscopus; 임원정scopus; 김수인scopus; 김선영scopus
Issue Date
2022
Journal Title
PSYCHOSOMATIC MEDICINE
ISSN
0033-3174JCR Link

1534-7796JCR Link
Citation
PSYCHOSOMATIC MEDICINE vol. 84, no. 7, pp. 757 - 765
Keywords
gut-brain axisgut microbiotadepressive symptomsASVs = amplicon sequence variantsBMI = body mass indexCES-D = Center for Epidemiologic Studies Rating Scale for DepressionFFQs = food frequency questionnairesMDD = major depressive disordersMaAsLin = multivariate association with linear modelsPICRUSt2=phylogenetic investigation of communities by reconstruction of unobserved states 2
Publisher
LIPPINCOTT WILLIAMS &

WILKINS
Indexed
SCIE; SSCI; SCOPUS WOS scopus
Document Type
Article
Abstract
Objective This study aimed to investigate the association between gut microbiota and depressive symptoms in a large population cohort of Korean adults. Methods Overall, 1238 participants were included in the study. Participants were categorized into depressed or non-depressed groups, based on the depressive symptoms reported on the Center for Epidemiologic Studies Rating Scale for Depression, with a cutoff score of 16, and their fecal microbiota was profiled using 16S ribosomal RNA gene sequencing. Several alpha and beta diversity measures were also estimated. The association between depressive symptoms and gut microbiota was analyzed using generalized linear models. The inferred function of the metagenomes was compared between the two groups. Results There were no consistent differences in alpha and beta diversity between the depressed and non-depressed groups. However, the continuous measure of depressive symptoms was inversely associated with one of four measures of alpha diversity (Shannon's diversity, p = .021). We also found a substantial difference between the depressed and non-depressed groups in the Bray-Curtis dissimilarity among the four beta diversity indices (p = .004). Participants whose depressive symptoms exceeded a clinical cutoff score had a lower relative abundance of the genus Faecalibacterium when compared with controls (coefficient = -0.025, q = 0.047). However, the depressed group had a significantly higher abundance of the genus Oscillospira than did the non-depressed group (coefficient = 0.002, q = 0.023). Conclusions Our findings contribute to the identification of potential relationships between the gut microbiota and depressive symptoms and provide useful insights for developing microbiota-based interventions for patients with depressive symptoms.
DOI
10.1097/PSY.0000000000001111
Appears in Collections:
의과대학 > 의학과 > Journal papers
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