Tseng Chin-Hsiao
Department of Internal Medicine, National Taiwan University College of Medicine, Taipei, Taiwan.
Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.
Oncotarget. 2016 Sep 20;7(38):62687-62696. doi: 10.18632/oncotarget.10507.
This study evaluated the risk of heart failure hospitalization in a 1:1 matched pair sample of sitagliptin ever and never users derived from the Taiwan's National Health Insurance. A total of 85,859 ever users and 85,859 never users matched on 8 digits of propensity score were followed for the first event of heart failure hospitalization until December 31, 2011. The treatment effect (for ever versus never users, and for tertiles of cumulative duration of therapy) was estimated by Cox regression incorporated with the inverse probability of treatment weighting using propensity score. Additionally, adjusted hazard ratios for heart failure were estimated for the baseline characteristics in sitagliptin ever users. Results showed that the incidence of heart failure hospitalization was 1,020.16 and 832.54 per 100,000 person-years, respectively, for ever and never users, with an overall hazard ratio (95% confidence intervals) of 1.262 (1.167-1.364). While compared to never users, the respective hazard ratio for the first, second, and third tertile of cumulative duration < 3.7, 3.7-10.3 and >10.3 months was 2.721 (2.449-3.023), 1.472 (1.318-1.645) and 0.515 (0.447-0.594). Older age, longer diabetes duration, male sex, and use of insulin, sulfonylurea, calcium channel blockers, aspirin, ticlopidine, clopidogrel and dipyridamole were significantly associated with a higher risk in sitagliptin users, but dyslipidemia and use of metformin and statin were protective. In conclusion, sitagliptin increases the risk of heart failure hospitalization within one year of its use, but reduces the risk thereafter. Some factors predisposing to sitagliptin-related heart failure are worthy of attention in clinical practice.
本研究在源自台湾全民健康保险的1:1匹配对样本中,评估了曾使用和从未使用西他列汀的患者发生心力衰竭住院的风险。对85859名曾使用者和85859名从未使用者进行了倾向评分的8位数字匹配,随访至2011年12月31日首次发生心力衰竭住院事件。采用Cox回归结合倾向评分的逆概率治疗权重法,估计治疗效果(曾使用者与从未使用者相比,以及治疗累积持续时间的三分位数)。此外,还对曾使用西他列汀患者的基线特征估计了心力衰竭的调整后风险比。结果显示,曾使用者和从未使用者的心力衰竭住院发生率分别为每10万人年1020.16例和832.54例,总体风险比(95%置信区间)为1.262(1.167 - 1.364)。与从未使用者相比,累积持续时间<3.7个月、3.7 - 10.3个月和>10.3个月的第一、第二和第三三分位数的相应风险比分别为2.721(2.449 - 3.023)、1.472(1.318 - 1.645)和0.515(0.447 - 0.594)。年龄较大、糖尿病病程较长、男性以及使用胰岛素、磺脲类药物、钙通道阻滞剂、阿司匹林、噻氯匹定、氯吡格雷和双嘧达莫与西他列汀使用者的较高风险显著相关,但血脂异常以及使用二甲双胍和他汀类药物具有保护作用。总之,西他列汀在使用一年内会增加心力衰竭住院风险,但此后会降低风险。一些易导致西他列汀相关心力衰竭的因素在临床实践中值得关注。