Fecal metaproteomics reveals alterations in gut microbiota and intestinal proteins in adolescents with bipolar depression

This study aims to compare the gut microbiota and the profiles of human and microbial proteins in adolescents with bipolar depression (BD) and healthy controls (HCs), as well as to investigate the potential of gut-derived proteins as biomarkers for BD diagnosis. Fecal samples were collected from 15 adolescents with depressive episodes of BD and 58 healthy individuals, and fecal metaproteomics was used to assess changes in the gut environment. The results revealed an increased abundance of gut bacteria associated with lactate production and metabolism, such as Bifidobacteriaceae and Megasphaera, in BD patients. Additionally, there was a higher abundance of Alistipes, a bacterium linked to stress. Notably, the host proteins CELA2A, DEFA3, and KLK1 achieved high ROC-AUC values (0.905, 0.897, and 0.897) and PR-AUC values (0.978, 0.975, and 0.975),indicating their potential as diagnostic biomarkers for BD. In conclusion, we observed an increased abundance of Bifidobacteriaceae, Megasphaera, and Alistipes in adolescents with BD. We propose that CELA2A, DEFA3, and KLK1 could be potential biomarkers for BD, although further validation is required.

Authors

Institutions

Publication Details

Journal
Translational Psychiatry
Published
2026-02-14
DOI
https://doi.org/10.1038/s41398-026-03899-6
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Fecal metaproteomics reveals alterations in gut microbiota and intestinal proteins in adolescents with bipolar depression

Yifan Tan, Xueying Li, Zixuan Zhao, Fangfang Zheng et al.
Translational Psychiatry
Gut microbiota and health
article

Fecal metaproteomics reveals alterations in gut microbiota and intestinal proteins in adolescents with bipolar depression

Yifan Tan, Xueying Li, Zixuan Zhao, Fangfang Zheng, Qixiao Lin, Jihui Yue, Xiaoqing Yin, Yong Lin, Fan Yang
article en

Abstract

This study aims to compare the gut microbiota and the profiles of human and microbial proteins in adolescents with bipolar depression (BD) and healthy controls (HCs), as well as to investigate the potential of gut-derived proteins as biomarkers for BD diagnosis. Fecal samples were collected from 15 adolescents with depressive episodes of BD and 58 healthy individuals, and fecal metaproteomics was used to assess changes in the gut environment. The results revealed an increased abundance of gut bacteria associated with lactate production and metabolism, such as Bifidobacteriaceae and Megasphaera, in BD patients. Additionally, there was a higher abundance of Alistipes, a bacterium linked to stress. Notably, the host proteins CELA2A, DEFA3, and KLK1 achieved high ROC-AUC values (0.905, 0.897, and 0.897) and PR-AUC values (0.978, 0.975, and 0.975),indicating their potential as diagnostic biomarkers for BD. In conclusion, we observed an increased abundance of Bifidobacteriaceae, Megasphaera, and Alistipes in adolescents with BD. We propose that CELA2A, DEFA3, and KLK1 could be potential biomarkers for BD, although further validation is required.

Translational PsychiatryVol. 16(1)
Sun Yat-sen University (CN), Fifth Affiliated Hospital of Sun Yat-sen University (CN)
Openalex Percentile: Top 56%
Gut microbiota and health
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Fecal metaproteomics reveals alterations in gut microbiota and intestinal proteins in adolescents with bipolar depression — Yifan Tan, Xueying Li, et al. · Translational Psychiatry (2026) | TGRS Research Map | TGRS