Xia Siliang, Liu Yun, Wang Mengzhu, Liu Dandan, Zhang Xiaobing, Lin Ling, Wen Ming, Ji Shushen, Li Jiaying, Zhang Xiangming, Jiang Huihui
Department of Cardiology, Nanjing Jiangbei Hospital, Nanjing, Jiangsu, China.
Zhangjiang Center for Translational Medicine, Shanghai Biotecan Pharmaceuticals Co., Ltd., Shanghai, China.
Front Immunol. 2025 Aug 13;16:1610001. doi: 10.3389/fimmu.2025.1610001. eCollection 2025.
Gut dysbiosis and the distribution of low-density lipoprotein cholesterol (LDL-C) subfractions have been implicated in cardiovascular risk among patients with ST-segment elevation myocardial infarction (STEMI). However, the prognostic significance of LDL-C subfractions in relation to gut microbiota composition remains largely unexplored. This study aimed to assess differences in gut microbiota profiles and LDL-C subfraction distribution between patients with STEMI with and without major adverse cardiovascular events (MACEs) and to elucidate their potential interplay.
We enrolled 32 male population without coronary heart disease and 66 male patients with STEMI. Fecal samples were analyzed via 16S rDNA gene sequencing to assess gut microbiota diversity and composition. Plasma LDL-C subfractions were quantified using the Quantimetrix Lipoprint LDL System.
Among these 66 STEMI patients, 18 experienced MACEs during a median follow-up of 13 months (MACEs group), while 18 age-matched event-free patients were selected as controls (Non-MACEs group). Significant differences in gut microbiota composition, but not diversity, were observed between the two groups, with the Non-MACEs group exhibiting a greater number of marker genera. Although no significant differences were found in LDL-C subfractions between groups, multiple significant negative correlations were identified between gut microbiota and LDL-C subfractions in the MACEs group, including between and LDLC-4 (ρ=-0.5488, P<0.05), between and LDLC-5 (ρ=-0.6418, P<0.01), between and LDLC-6 (ρ=-0.4988, P<0.05), between and LDLC-4 (ρ=-0.4948, P<0.05), and between and LDLC-4 (ρ=-0.5032, P<0.05). Furthermore, gut microbiota markers demonstrated superior predictive performance for MACEs compared to LDL-C subfractions, with , , and achieving AUC values >0.75.
Gut microbiota, particularly , , and , exhibit greater prognostic potential for MACEs than LDL-C subfractions. These findings highlight the role of gut microbiota in post-STEMI risk stratification, underscoring its potential as a target for future cardiovascular interventions.
肠道菌群失调和低密度脂蛋白胆固醇(LDL-C)亚组分的分布与ST段抬高型心肌梗死(STEMI)患者的心血管风险有关。然而,LDL-C亚组分与肠道微生物群组成的预后意义在很大程度上仍未得到探索。本研究旨在评估发生和未发生主要不良心血管事件(MACE)的STEMI患者之间肠道微生物群谱和LDL-C亚组分分布的差异,并阐明它们之间的潜在相互作用。
我们纳入了32名无冠心病的男性人群和66名男性STEMI患者。通过16S rDNA基因测序分析粪便样本,以评估肠道微生物群的多样性和组成。使用Quantimetrix Lipoprint LDL系统对血浆LDL-C亚组分进行定量。
在这66名STEMI患者中,18名在中位随访13个月期间发生了MACE(MACE组),而选择18名年龄匹配的无事件患者作为对照(非MACE组)。两组之间在肠道微生物群组成而非多样性方面存在显著差异,非MACE组表现出更多的标志性属。虽然两组之间在LDL-C亚组分方面未发现显著差异,但在MACE组中,肠道微生物群与LDL-C亚组分之间发现了多个显著的负相关,包括与LDLC-4之间(ρ=-0.5488,P<0.05)、与LDLC-5之间(ρ=-0.6418,P<0.01)、与LDLC-6之间(ρ=-0.4988,P<0.05)、与LDLC-4之间(ρ=-0.4948,P<0.05)以及与LDLC-4之间(ρ=-0.5032,P<0.05)。此外,与LDL-C亚组分相比,肠道微生物群标志物对MACE具有更好的预测性能,其中、和的AUC值>0.75。
肠道微生物群,特别是、和,对MACE的预后潜力比LDL-C亚组分更大。这些发现突出了肠道微生物群在STEMI后风险分层中的作用,强调了其作为未来心血管干预靶点的潜力。