TY - JOUR
T1 - Association Between Gut Microbiota and Depressive Symptoms
T2 - A Cross-Sectional Population-Based Study in South Korea
AU - Kim, Sun Young
AU - Park, Eunkyo
AU - Lim, Weon Jeong
AU - In Kim, Soo
AU - Jeon, Sang Won
AU - Chang, Yoosoo
AU - Ryu, Seungho
AU - Kim, Hyung Lae
AU - Kim, Han Na
N1 - Funding Information:
Source of Funding and Conflicts of Interest: This research was funded by the Basic Science Research Program through the National Research Foundation of Korea funded by the Ministry of Education (NRF-2021R1I1A1A01051484, Sun-Young Kim, 50% and NRF-2020R1A2C1012931, Han-Na Kim, 50%). The funding source had no further role in the study design, preparation, writing of the report, or the decision to submit this article for publication. The authors declare that they have no conflict of interest.
Publisher Copyright:
© Lippincott Williams & Wilkins.
PY - 2022/9
Y1 - 2022/9
N2 - 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.
AB - 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.
KW - ASVs = amplicon sequence variants
KW - BMI = body mass index
KW - CES-D = Center for Epidemiologic Studies Rating Scale for Depression
KW - FFQs = food frequency questionnaires
KW - MDD = major depressive disorders
KW - MaAsLin = multivariate association with linear models
KW - PICRUSt2 = phylogenetic investigation of communities by reconstruction of unobserved states 2
KW - depressive symptoms
KW - gut microbiota
KW - gut-brain axis
UR - http://www.scopus.com/inward/record.url?scp=85137136975&partnerID=8YFLogxK
U2 - 10.1097/PSY.0000000000001111
DO - 10.1097/PSY.0000000000001111
M3 - Article
C2 - 35980774
AN - SCOPUS:85137136975
SN - 0033-3174
VL - 84
SP - 757
EP - 765
JO - Psychosomatic Medicine
JF - Psychosomatic Medicine
IS - 7
ER -