Zhou Xinyu, Liu Ying, Guo Ying, Wang Ning, Wang Siyuan, Song Jiawei, Dong Zhaojie, Yang Xiaoyan, Chen Yufei, Li Jing, Zhao Lin, Dong Ying, Zhong Jiuchang
Heart Center and Beijing Key Laboratory of Hypertension, Beijing Chaoyang Hospital, Capital Medical University, 8th Gongtinanlu Rd, Chaoyang District, Beijing, 100020, China.
Department of Cardiology, Beijing Chaoyang Hospital, Capital Medical University, Beijing, 100020, China.
Intern Emerg Med. 2025 Aug 30. doi: 10.1007/s11739-025-04092-1.
The exact role of SIRT7 in hypertensive patients with coronary artery disease (CAD) remains elusive. This study aimed to explore plasma SIRT7 levels and their clinical significance in this population. From July 2022 to June 2024, 222 hypertensive patients (106 with isolated hypertension and 116 with hypertension plus CAD) were enrolled. Plasma SIRT7 was measured by ELISA, and participants were followed for rehospitalization (median 804 days). ROC curves, LASSO regression, and Cox proportional hazards models were used for statistical analysis. Hypertensive CAD patients had significantly higher SIRT7 levels than those without CAD (P < 0.001). Plasma SIRT7 levels were positively correlated with CK (R = 0.36, P < 0.001) and CK-MB (R = 0.50, P < 0.001), and negatively with HDL-C (R = -0.23, P < 0.001). The optimal cutoff of SIRT7 for diagnosing CAD demonstrated 94.0% sensitivity and 75.5% specificity, exhibiting an AUC of 0.917, superior to CK, CK-MB, and HDL-C. Multivariate analysis identified SIRT7 as an independent CAD risk factor (adjusted OR = 1.97, 95% CI 1.48-2.63). Restricted cubic spline (RCS) analysis revealed a linear correlation between SIRT7 and rehospitalization (P for overall = 0.038), but no non-linear relationship (P for non-linear = 0.164). Elevated SIRT7 predicted rehospitalization risk (HR = 1.15, 95% CI 1.02-1.29) and improved risk prediction, with an integrated discrimination index (IDI) of 21.8% and net reclassification improvement (NRI) of 51.0%. Plasma SIRT7 acts as both a diagnostic marker for CAD and a predictor of rehospitalization in hypertensive patients, indicating its dual role in pathogenesis and clinical monitoring. Targeting SIRT7 signaling may offer a new therapeutic strategy for hypertension-associated CAD.
SIRT7在高血压合并冠状动脉疾病(CAD)患者中的具体作用仍不明确。本研究旨在探讨该人群血浆SIRT7水平及其临床意义。2022年7月至2024年6月,纳入222例高血压患者(106例单纯高血压患者和116例高血压合并CAD患者)。采用酶联免疫吸附测定法(ELISA)检测血浆SIRT7水平,并对参与者进行再住院随访(中位时间804天)。采用ROC曲线、LASSO回归和Cox比例风险模型进行统计分析。高血压合并CAD患者的SIRT7水平显著高于无CAD患者(P<0.001)。血浆SIRT7水平与肌酸激酶(CK)(R = 0.36,P<0.001)和肌酸激酶同工酶(CK-MB)(R = 0.50,P<0.001)呈正相关,与高密度脂蛋白胆固醇(HDL-C)呈负相关(R = -0.23,P<0.001)。SIRT7诊断CAD的最佳截断值显示敏感性为94.0%,特异性为75.5%,曲线下面积(AUC)为0.917,优于CK、CK-MB和HDL-C。多因素分析确定SIRT7为CAD的独立危险因素(调整后比值比[OR]=1.97,95%置信区间[CI] 1.48-2.63)。受限立方样条(RCS)分析显示SIRT7与再住院之间存在线性相关性(总体P = 0.038),但不存在非线性关系(非线性P = 0.164)。SIRT7升高可预测再住院风险(风险比[HR]=1.15,95%CI 1.02-1.29),并改善风险预测,综合判别指数(IDI)为21.8%,净重新分类改善(NRI)为51.0%。血浆SIRT7既是CAD的诊断标志物,也是高血压患者再住院的预测指标,表明其在发病机制和临床监测中的双重作用。靶向SIRT7信号通路可能为高血压相关CAD提供一种新的治疗策略。