肠道菌群
肠道微生物群
微生物群
粪便细菌疗法
生物
疾病
人体研究
肠道细菌
生物信息学
人体微生物群
肠-脑轴
益生菌
失调
临床试验
移植
免疫学
医学
动物研究
肠道菌群
评论文章
基因组
计算生物学
电流(流体)
胆汁酸
人类微生物组计划
重症监护医学
作者
S.X. Zhang,Jing‐Feng Li,Liping Li,Xingxing Yuan
标识
DOI:10.3389/fmicb.2025.1690411
摘要
The gut microbiome has emerged as a critical modulator of cardiovascular disease (CVD) risk, offering a novel frontier for therapeutic intervention. This mini-review synthesizes current evidence on how probiotic-like bacteria and their metabolites mediate protective physiological mechanisms against CVD. Drawing from both animal models and human clinical trials, we elucidate the biological pathways, including trimethylamine-N-oxide (TMAO), short-chain fatty acids (SCFAs), and bile acid metabolism, through which the gut microbiota influences hypertension, atherosclerosis, and heart failure. Furthermore, we examine microbiota-based strategies such as dietary modification, fecal microbiota transplantation (FMT), and pharmacological agents aimed at restoring microbial homeostasis. Despite promising mechanistic insights, human trials have yet to consistently demonstrate significant clinical benefits in reversing CVD outcomes via gut microbiota modulation. This review underscores the necessity of moving from correlation to causation, highlighting current limitations and future prospects for leveraging gut microbiome research in the development of personalized, effective therapeutic strategies for cardiovascular diseases.
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