State Key Laboratory of Pathogenesis, Prevention and Treatment of High Incidence Diseases in Central Asia, Urumqi, China.
Department of Cardiology, First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
BMC Cardiovasc Disord. 2023 Jun 3;23(1):284. doi: 10.1186/s12872-023-03223-w.
To investigate the possible association between AT1R gene polymorphisms and major adverse cardiovascular and cerebrovascular events (MACCEs) in hypertension patients combined with or without coronary artery disease (CAD) in Xinjiang.
374 CAD patients and 341 non-CAD individuals were enrolled as study participants and all of them have a hypertension diagnosis. AT1R gene polymorphisms were genotyped by SNPscan™ typing assays. During the follow-up in the clinic or by telephone interview, MACCEs were recorded. Kaplan-Meier curves and Cox survival analyses were used to explore the association between AT1R gene polymorphisms and the occurrence of MACCEs.
AT1R gene rs389566 was associated with MACCEs. The TT genotype of the AT1R gene rs389566 had a significantly higher probability of MACCEs than the AA + AT genotype (75.2% vs. 24.8%, P = 0.033). Older age (OR = 1.028, 95% CI: 1.009-1.0047, P = 0.003) and TT genotype of rs389566 (OR = 1.770, 95% CI: 1.148-2.729, P = 0.01) were risk factors of MACCEs. AT1R gene rs389566 TT genotype may be a predisposing factor for the occurrence of MACCEs in hypertensive patients.
We should also pay more attention to the prevent of MACCEs in hypertension patients combined with CAD. Especially those elderly hypertensive patients carrying AT1R rs389566 TT genotype requires avoidance of unhealthy lifestyle, better management of blood pressure control and reduce the occurrence of MACCEs.
探讨血管紧张素Ⅱ受体 1(AT1R)基因多态性与新疆地区高血压合并或不合并冠状动脉疾病(CAD)患者主要不良心脑血管事件(MACCEs)的相关性。
选取 374 例 CAD 患者和 341 例非 CAD 个体作为研究对象,所有患者均被诊断为高血压。采用 SNPscan™ 基因分型试剂盒检测 AT1R 基因多态性。在临床随访或电话随访中记录 MACCEs 的发生情况。采用 Kaplan-Meier 曲线和 Cox 生存分析探讨 AT1R 基因多态性与 MACCEs 发生的相关性。
AT1R 基因 rs389566 与 MACCEs 相关。与 AA+AT 基因型相比,AT1R 基因 rs389566 的 TT 基因型发生 MACCEs 的概率明显更高(75.2% vs. 24.8%,P=0.033)。年龄较大(OR=1.028,95%CI:1.009-1.0047,P=0.003)和 rs389566 的 TT 基因型(OR=1.770,95%CI:1.148-2.729,P=0.01)是 MACCEs 的危险因素。AT1R 基因 rs389566 的 TT 基因型可能是高血压患者发生 MACCEs 的易患因素。
对于合并 CAD 的高血压患者,我们还应更加关注 MACCEs 的预防。特别是那些携带 AT1R rs389566 TT 基因型的老年高血压患者,需要避免不健康的生活方式,更好地控制血压,减少 MACCEs 的发生。