Cho A-Ra, Heo Seok-Jae, Han Taehwa, Kwon Yu-Jin
Department of Family Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Department of Family Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.
J Clin Hypertens (Greenwich). 2025 Mar;27(3):e70035. doi: 10.1111/jch.70035.
Cardiovascular mortality is a leading cause of global deaths, with aging, dyslipidemia, and inflammation recognized as key risk factors. This study aimed to identify distinct cardiovascular risk profiles using cluster analysis based on lipid profiles and inflammatory markers in a large cohort of middle-aged Korean adults. Our analysis included 8115 participants without cardiovascular disease (CVD) at baseline from the Korean Genome and Epidemiology Study. We applied the K-means clustering algorithm to conduct a cluster analysis of six normalized variables: age, total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), non-HDL-C, and CRP. Multivariable Cox proportional-hazard regression analysis was performed to assess the hazard ratio with 95% confidence interval for CVD incidence, CVD mortality, major adverse cardiac event (MACE) mortality, and all-cause mortality. Four clusters were identified based on age, lipids (TC, TG, HDL-C, non-HDL-C), and CRP. Cluster 1 (older age, high CRP) and cluster 2 (high TC, non-HDL-C, insulin resistance) had the highest risks for new-onset CVD, while cluster 1 had the highest risks for all-cause and cardiovascular mortality. Cluster 3 (high HDL-C) showed a lower CVD risk, while cluster 4 (younger age, favorable lipid profile) had the lowest risk across all outcomes. This study highlighted the combined impact of aging, dyslipidemia, and inflammation on CVD risk. The clusters with older age and high inflammation or dyslipidemia had the highest cardiovascular risks, emphasizing the importance of managing these factors in high-risk populations.
心血管疾病死亡率是全球死亡的主要原因,衰老、血脂异常和炎症被认为是关键风险因素。本研究旨在基于脂质谱和炎症标志物,通过聚类分析在一大群中年韩国成年人中识别不同的心血管风险特征。我们的分析纳入了韩国基因组与流行病学研究中8115名基线时无心血管疾病(CVD)的参与者。我们应用K均值聚类算法对六个标准化变量进行聚类分析:年龄、总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、非HDL-C和CRP。进行多变量Cox比例风险回归分析,以评估CVD发病率、CVD死亡率、主要不良心脏事件(MACE)死亡率和全因死亡率的风险比及95%置信区间。根据年龄、脂质(TC、TG、HDL-C、非HDL-C)和CRP识别出四个聚类。聚类1(年龄较大、CRP较高)和聚类2(TC、非HDL-C较高、胰岛素抵抗)新发CVD风险最高,而聚类1全因死亡率和心血管疾病死亡率风险最高。聚类3(HDL-C较高)显示CVD风险较低,而聚类4(年龄较小、脂质谱良好)在所有结局中风险最低。本研究强调了衰老、血脂异常和炎症对CVD风险的综合影响。年龄较大且炎症或血脂异常较高的聚类心血管风险最高,强调了在高危人群中管理这些因素的重要性。