a Department of Health Behavior and Health Education, Institute of Clinical Epidemiology, Key Laboratory of Public Health Safety, Ministry of Education, School of Public Health , Fudan University , Shanghai , China.
b Department of Community Health and Behavioral Medicine, School of Public Health , Shanghai Jiao Tong University , Shanghai , China.
Clin Exp Hypertens. 2019;41(3):244-254. doi: 10.1080/10641963.2018.1469640. Epub 2018 May 21.
This study aimed to compare the real-world effectiveness of valsartan and non renin-angiotensin system (non-RAS) agent monotherapy on the incidence of new on-set diabetes (NOD) in Chinese hypertensive patients. It was based on an electronic Health Recording System database from Minhang District of Shanghai. Hypertensive patients aged ≥18 years continuously taking either valsartan or non-RAS agent monotherapy for >12 months were included. Hazard ratios (HR) of NOD events were estimated using propensity score matching method and multivariate regression. Of 29295 patients, there were 2107 in valsartan group, 21397 in CCB group, 4094 in β-blockers group and 1697 in diuretics group. Two-year follow-up revealed NOD rates of 11.09 and 14.22 per 100 persons per year in valsartan and non-RAS inhibitor groups (HR = 0.77, 95% confidence interval 0.65-0.93, P = 0.006), respectively. Among non-RAS agents, CCB group had the highest incidence of NOD (21.72 per 100 persons per year). Comparisons between CCB sub-groups revealed the highest NOD incidence for nifedipine, followed by amlodipine and felodipine. NOD incidences in β-blockers and diuretics groups (11.70 and 10.50 per 100 persons per year, respectively) were not significantly different from valsartan group. Compared with non-RAS inhibitors, particularly CCBs, valsartan could significantly reduce the incidence of NOD.
本研究旨在比较缬沙坦和非肾素-血管紧张素系统(非 RAS)单药治疗在新发糖尿病(NOD)发生率方面的真实世界疗效,其数据来源于上海市闵行区电子健康记录系统数据库。纳入的高血压患者需满足年龄≥18 岁、连续服用缬沙坦或非 RAS 单药治疗≥12 个月的条件。使用倾向评分匹配法和多变量回归来估计 NOD 事件的风险比(HR)。在 29295 名患者中,缬沙坦组有 2107 人,CCB 组有 21397 人,β受体阻滞剂组有 4094 人,利尿剂组有 1697 人。在为期 2 年的随访中,缬沙坦组和非 RAS 抑制剂组的 NOD 发生率分别为 11.09 和 14.22/100 人年(HR=0.77,95%置信区间 0.65-0.93,P=0.006)。在非 RAS 药物中,CCB 组的 NOD 发生率最高(21.72/100 人年)。CCB 亚组之间的比较显示,硝苯地平的 NOD 发生率最高,其次是氨氯地平和非洛地平。β受体阻滞剂组和利尿剂组的 NOD 发生率(分别为 11.70 和 10.50/100 人年)与缬沙坦组无显著差异。与非 RAS 抑制剂,特别是 CCB 相比,缬沙坦可显著降低 NOD 的发生率。