Integrative analysis of the gut microbiota, bile acid pathways, and immune dysregulation in dyslipidemia models

Emerging evidence suggests a link between gut microbiota, bile acid metabolism, and immune dysregulation in dyslipidemia. Through a case-control study involving 140 participants and an animal experiment, we identified significantly elevated counts of peripheral blood CD3<sup>+</sup> T cells, CD4<sup>+</sup> T cells, CD8<sup>+</sup> T cells, and CD19<sup>+</sup> B cells in patients with dyslipidemia, alongside increased specific bile acids in fecal samples and distinct alterations in gut microbiota composition. The animal model confirmed changes in gut microbiota, bile acid metabolism, and percentage of specific lymphocyte subsets. Also, we identified downregulated hepatic expressions of bile acid metabolism-related proteins in hyperlipidemic rats. Integrated analysis suggested potential associations among gut microbiota, bile acid pathways, and immune dysregulation. Overall, these data highlight the critical role of the potential gut microbiota-bile acid metabolism-immune axis in dyslipidemia, providing potential therapeutic targets for diseases associated with lipid metabolism disorders.

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Journal
iScience
Published
2025-11-11
DOI
https://doi.org/10.1016/j.isci.2025.114001
Primary Topic
Gut microbiota and health
Type
article
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article

Integrative analysis of the gut microbiota, bile acid pathways, and immune dysregulation in dyslipidemia models

J.P. Wang, Guiju Sun, Ze Zhang, Zhiyuan Feng et al.
iScience
Gut microbiota and health
article

Integrative analysis of the gut microbiota, bile acid pathways, and immune dysregulation in dyslipidemia models

J.P. Wang, Guiju Sun, Ze Zhang, Zhiyuan Feng, Shiyu Yin, Yu Shao, Jiayue Xia, Bin Li, Yuanyuan Wang, Zhi He, Junhui Yu, Tianyu Wu
article en

Abstract

Emerging evidence suggests a link between gut microbiota, bile acid metabolism, and immune dysregulation in dyslipidemia. Through a case-control study involving 140 participants and an animal experiment, we identified significantly elevated counts of peripheral blood CD3<sup>+</sup> T cells, CD4<sup>+</sup> T cells, CD8<sup>+</sup> T cells, and CD19<sup>+</sup> B cells in patients with dyslipidemia, alongside increased specific bile acids in fecal samples and distinct alterations in gut microbiota composition. The animal model confirmed changes in gut microbiota, bile acid metabolism, and percentage of specific lymphocyte subsets. Also, we identified downregulated hepatic expressions of bile acid metabolism-related proteins in hyperlipidemic rats. Integrated analysis suggested potential associations among gut microbiota, bile acid pathways, and immune dysregulation. Overall, these data highlight the critical role of the potential gut microbiota-bile acid metabolism-immune axis in dyslipidemia, providing potential therapeutic targets for diseases associated with lipid metabolism disorders.

iScienceVol. 28(12)
Zhongda Hospital Southeast University (CN), Southeast University (CN)
Openalex Percentile: Top 70%
Gut microbiota and health
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