Gut microbiota: A bridge between depression and cardiovascular disease-A narrative review

Xingdou Mu , Lele Feng , Hong Li , Yang Sun
{"title":"Gut microbiota: A bridge between depression and cardiovascular disease-A narrative review","authors":"Xingdou Mu ,&nbsp;Lele Feng ,&nbsp;Hong Li ,&nbsp;Yang Sun","doi":"10.1016/j.microb.2025.100292","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Depression and cardiovascular disease (CVD) exhibit a bidirectional relationship, with individuals suffering from either condition facing elevated risks of comorbidity and mortality. Emerging evidence highlights the gut microbiota (GM) as a critical mediator in this interaction.</div></div><div><h3>Methods</h3><div>This narrative review synthesizes current research on the role of GM and its metabolites in linking depression and CVD.</div></div><div><h3>Results</h3><div>Dysbiosis of GM is consistently observed in both conditions, characterized by reduced microbial diversity, decreased abundance of beneficial bacteria (e.g., Faecalibacterium, Roseburia), and increased pro-inflammatory species (e.g., Enterobacteriaceae). Key microbial metabolites, including short-chain fatty acids (SCFAs), trimethylamine N-oxide (TMAO), and indole-3-propionic acid (IPA), influence neuroendocrine, immune, and metabolic pathways. For instance, SCFAs modulate neuroinflammation and endothelial function, while TMAO exacerbates atherosclerosis. Depression-associated GM alterations disrupt the gut-brain axis via the hypothalamic-pituitary-adrenal (HPA) axis and vagus nerve, whereas CVD-related dysbiosis promotes systemic inflammation and endothelial dysfunction. Shared mechanisms, such as NLRP3 inflammasome activation and bile acid metabolism dysregulation, further connect these diseases. Therapeutic strategies targeting GM probiotics, dietary interventions, fecal microbiota transplantation (FMT), and metabolite modulation may alleviate both conditions. However, challenges remain in addressing heterogeneity across studies, establishing causal relationships, and optimizing personalized interventions. Future research should integrate multi-omics approaches and longitudinal studies to unravel the gut-brain-heart axis, paving the way for precision therapies.</div></div><div><h3>Conclusions</h3><div>This review underscores GM’s pivotal role in depression and CVD comorbidity, offering novel insights for clinical management and interdisciplinary treatment strategies.</div></div>","PeriodicalId":101246,"journal":{"name":"The Microbe","volume":"7 ","pages":"Article 100292"},"PeriodicalIF":0.0000,"publicationDate":"2025-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Microbe","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2950194625000603","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Depression and cardiovascular disease (CVD) exhibit a bidirectional relationship, with individuals suffering from either condition facing elevated risks of comorbidity and mortality. Emerging evidence highlights the gut microbiota (GM) as a critical mediator in this interaction.

Methods

This narrative review synthesizes current research on the role of GM and its metabolites in linking depression and CVD.

Results

Dysbiosis of GM is consistently observed in both conditions, characterized by reduced microbial diversity, decreased abundance of beneficial bacteria (e.g., Faecalibacterium, Roseburia), and increased pro-inflammatory species (e.g., Enterobacteriaceae). Key microbial metabolites, including short-chain fatty acids (SCFAs), trimethylamine N-oxide (TMAO), and indole-3-propionic acid (IPA), influence neuroendocrine, immune, and metabolic pathways. For instance, SCFAs modulate neuroinflammation and endothelial function, while TMAO exacerbates atherosclerosis. Depression-associated GM alterations disrupt the gut-brain axis via the hypothalamic-pituitary-adrenal (HPA) axis and vagus nerve, whereas CVD-related dysbiosis promotes systemic inflammation and endothelial dysfunction. Shared mechanisms, such as NLRP3 inflammasome activation and bile acid metabolism dysregulation, further connect these diseases. Therapeutic strategies targeting GM probiotics, dietary interventions, fecal microbiota transplantation (FMT), and metabolite modulation may alleviate both conditions. However, challenges remain in addressing heterogeneity across studies, establishing causal relationships, and optimizing personalized interventions. Future research should integrate multi-omics approaches and longitudinal studies to unravel the gut-brain-heart axis, paving the way for precision therapies.

Conclusions

This review underscores GM’s pivotal role in depression and CVD comorbidity, offering novel insights for clinical management and interdisciplinary treatment strategies.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
The antibacterial and antioxidant activities of plumbagin-rich methanolic root extracts from Plumbago zeylanica L. In vitro antibacterial spectra and analysis of antimicrobal bioactive compound of Bacillus subtilis ASPL1 isolated from the soil of Ajodhya hill forest Effect of dietary supplementation of Fructobacillus fructosus MCC 3996 on body weight, serum lipid and liver histopathology of high‑fat diet-fed swiss albino mice Lichenomics: Exploring bioactive compounds with anti-tumor potential in colon cancer cell lines Gut microbiota: A bridge between depression and cardiovascular disease-A narrative review
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1