Lai Hongmei, Zhu Jinhang, Tao Jing, Guo Zitong, Yu Xiaolin, Shen Xin, Wang Ting, Wang Ying, Cai Huan, Cai Xiao, Wei Zhenbang, Yang Yining
The Cardiac and Panvascular Medicine Diagnosis and Treatment Center, People's Hospital of Xinjiang Uyghur Autonomous Region, Xinjiang, China.
Xinjiang Key Laboratory of Cardiovascular Homeostasis and Regeneration Research, Xinjiang, China.
Front Pharmacol. 2025 Aug 15;16:1588658. doi: 10.3389/fphar.2025.1588658. eCollection 2025.
Acute coronary syndrome (ACS) is a critical cardiovascular condition with diverse clinical presentations, necessitating personalized therapeutic approaches. This study explores the genetic variation associated with ACS subtypes in the Han and Uyghur Chinese populations to support the development of precision medicine approaches tailored to ethnic-specific genetic backgrounds.
A total of 985 ACS patients (668 Han and 317 Uyghur Chinese) representing different ACS subtypes were enrolled. Clinical characteristics and 66 genetic polymorphisms were analyzed. Statistical analyses were conducted to identify differences in genetic variants and clinical features across ACS subtypes and ethnic groups.
Significant clinical and genetic differences were observed between ACS subtypes and between ethnic groups. In the Han population, polymorphisms in and were significantly associated with ACS subtypes ( ≤ 0.05). In the Uyghur population, six genes-, , , , , and -showed significant associations ( ≤ 0.05). These findings indicate distinct genetic landscapes across the two ethnic groups. Furthermore, population-specific associations between genetic variants and artery narrowing were identified. Predictive models integrating clinical and genetic features achieved an area under the curve (AUC) of 0.832 [95% confidence intervals (CI): 0.774-0.889] in Uyghur patients and 0.674 (95% CI: 0.626-0.722) in Han patients, indicating a higher internal AUC of these genetic markers in the Uyghur population.
This study highlights ethnic differences in the genetic architecture of ACS. The result also underscores the need for population-specific strategies in risk stratification and treatment. The identified genetic markers and predictive models may guide future research on ethnicity-specific risk stratification.
急性冠状动脉综合征(ACS)是一种严重的心血管疾病,临床表现多样,需要个性化的治疗方法。本研究探讨了汉族和维吾尔族人群中与ACS亚型相关的基因变异,以支持针对特定种族基因背景的精准医学方法的发展。
共纳入985例代表不同ACS亚型的患者(汉族668例,维吾尔族317例)。分析了临床特征和66个基因多态性。进行统计分析以确定ACS亚型和种族之间基因变异和临床特征的差异。
在ACS亚型之间以及种族之间观察到显著的临床和基因差异。在汉族人群中,[具体基因名称1]和[具体基因名称2]的多态性与ACS亚型显著相关(P≤0.05)。在维吾尔族人群中,六个基因——[具体基因名称3]、[具体基因名称4]、[具体基因名称5]、[具体基因名称6]、[具体基因名称7]和[具体基因名称8]——显示出显著关联(P≤0.05)。这些发现表明两个种族之间存在不同的基因格局。此外,还确定了基因变异与动脉狭窄之间的种族特异性关联。整合临床和基因特征的预测模型在维吾尔族患者中的曲线下面积(AUC)为0.832 [95%置信区间(CI):0.774 - 0.889],在汉族患者中为0.674(95% CI:0.626 - 0.722),表明这些基因标记在维吾尔族人群中的内部AUC更高。
本研究突出了ACS基因结构中的种族差异。结果还强调了在风险分层和治疗中采用针对特定人群策略的必要性。所确定的基因标记和预测模型可能会指导未来关于特定种族风险分层的研究。