Long-term Metformin Alters Gut Microbiota and Serum Metabolome in Coronary Artery Disease Patients After Percutaneous Coronary Intervention to Improve 5-year Prognoses: A Multi-omics Analysis.

IF 1.9 4区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS
Reviews in cardiovascular medicine Pub Date : 2025-05-27 eCollection Date: 2025-05-01 DOI:10.31083/RCM26835
Ruilin Zhou, Qingyang Wu, Hao Qian, Liang Wang, Guangcheng Liu, Bin Zhang, Wei Wu, Shuyang Zhang
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引用次数: 0

Abstract

Background: About 20% of patients with coronary artery disease (CAD) experience adverse events within five years of undergoing percutaneous coronary intervention (PCI) for acute myocardial infarction. In these patients, the impact of metformin on long-term prognosis remains uncertain.

Methods: This study enrolled 22 metformin (Met)-CAD patients with diabetes mellitus (DM) who had been administered metformin for at least six months before PCI, 14 non-Met CAD-DM patients with DM who had never taken metformin or had stopped taking metformin for a year before PCI, and 22 matched healthy controls. A 5-year follow-up was conducted to collect clinical prognosis data. Fecal 16S rRNA sequencing and serum untargeted metabolomics analyses were performed. BugBase was utilized to analyze the possible functional changes in the gut microbiome. Multi-omics analysis was conducted using Spearman's correlation to explore the interactions between metformin, gut microbiome, serum metabolites, and clinical prognosis.

Results: Metformin significantly lowered the 5-year major adverse cardiac events (MACEs) in Met CAD-DM patients. We found a higher abundance of Bacteroides coprocola, Bacteroides massiliensis, Phascolarctobacterium succinatutens, and Eubacterium coprostanoligenes in the Met CAD-DM patients, as well as an increase in hydroxy-alpha-sanshool (HAS) and decenoylcarnitine and a decrease in tridec-10-enoic acid, Z-vad-fmk (benzyloxycarbonyl-Val-Ala-Asp (OMe)-fluoromethylketone), 3,9-dimethyluric acid in blood serum. Multi-omics analysis revealed that alterations in the gut microbiome and serum metabolites are significantly associated with the 5-year prognosis of CAD-DM.

Conclusions: Metformin significantly improved the 5-year prognosis of CAD patients following PCI. Metformin tended to have more positive effects on the commensal flora and metabolic profiles, which may explain its beneficial effects on cardiovascular health. This study revealed the potential associations between metformin and the gut microbiome, an associated alteration in serum metabolome, and the impact on the host immune system and metabolic pathways.

长期二甲双胍改变经皮冠状动脉介入治疗后冠心病患者的肠道微生物群和血清代谢组改善5年预后:一项多组学分析
背景:大约20%的冠状动脉疾病(CAD)患者在接受急性心肌梗死经皮冠状动脉介入治疗(PCI)后5年内出现不良事件。在这些患者中,二甲双胍对长期预后的影响仍不确定。方法:本研究纳入了22例在PCI前已接受二甲双胍治疗至少6个月的二甲双胍-CAD合并糖尿病(DM)患者,14例在PCI前从未服用过二甲双胍或停止服用二甲双胍一年的非Met CAD-DM合并DM患者,以及22例匹配的健康对照。随访5年,收集临床预后资料。进行粪便16S rRNA测序和血清非靶向代谢组学分析。利用BugBase分析肠道微生物组可能的功能变化。采用Spearman’s correlation进行多组学分析,探讨二甲双胍与肠道微生物组、血清代谢物和临床预后之间的相互作用。结果:二甲双胍显著降低Met CAD-DM患者5年主要不良心脏事件(mace)。我们发现Met CAD-DM患者中coprocola拟杆菌、masiliensis拟杆菌、succinatutens Phascolarctobacterium和coprostanoligene真杆菌的丰度较高,血清中羟基- α -三酚(HAS)和十二烷基肉碱含量增加,血清中三烯-10-烯酸、Z-vad-fmk (benzyloxycarbonyl- vala - asp (OMe)-氟甲基酮)、3,9-二甲基尿酸含量减少。多组学分析显示,肠道微生物组和血清代谢物的改变与CAD-DM的5年预后显著相关。结论:二甲双胍可显著改善冠心病患者PCI术后5年预后。二甲双胍往往对共生菌群和代谢谱有更积极的影响,这可以解释其对心血管健康的有益作用。这项研究揭示了二甲双胍与肠道微生物组、血清代谢组的相关改变以及对宿主免疫系统和代谢途径的影响之间的潜在关联。
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来源期刊
Reviews in cardiovascular medicine
Reviews in cardiovascular medicine 医学-心血管系统
CiteScore
2.70
自引率
3.70%
发文量
377
审稿时长
1 months
期刊介绍: RCM is an international, peer-reviewed, open access journal. RCM publishes research articles, review papers and short communications on cardiovascular medicine as well as research on cardiovascular disease. We aim to provide a forum for publishing papers which explore the pathogenesis and promote the progression of cardiac and vascular diseases. We also seek to establish an interdisciplinary platform, focusing on translational issues, to facilitate the advancement of research, clinical treatment and diagnostic procedures. Heart surgery, cardiovascular imaging, risk factors and various clinical cardiac & vascular research will be considered.
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