...
首页> 外文期刊>Pharmacoepidemiology and drug safety >Statins of high versus low cholesterol-lowering efficacy and the development of severe renal failure
【24h】

Statins of high versus low cholesterol-lowering efficacy and the development of severe renal failure

机译:他汀类药物的降血脂药疗效高低与严重肾衰竭的发生有关

获取原文
获取原文并翻译 | 示例

摘要

Background: The objective of this nationwide retrospective cohort study was to examine the renal outcomes of HMG-CoA reductase inhibitor (statin) initiators. Methods: The patients who started to take statins with high cholesterol-lowering efficacy (atorvastatin and rosuvastatin) and low efficacy (lovastatin, simvastatin, pravastatin, and fluvastatin) between 1 January 2001 and 31 December 2008 were identified from the Taiwan National Health Insurance claims database. The outcome of interest was severe renal failure, defined as the composite endpoint of hemodialysis, peritoneal dialysis, and kidney transplantation. A proportional hazard regression model was applied to estimate the incidence ratio between the two groups, adjusted for the propensity scores based upon baseline characteristics. Results: Among of the 26007 and 42249 statin initiators, the crude incidence rate for developing severe renal failure was 0.65 and 0.46 per 100 person-years for the high-efficacy and low-efficacy groups, respectively. Despite that these two groups had comparable risk for myocardial infarction (hazard ratio: 1.06, 95%CI: 0.92-1.21), there was a 13% increased hazard for developing severe renal failure in the rosuvastatin and atorvastatin initiators (hazard ratio: 1.13, 95%CI: 1.02-1.26). The increased risk associated with these two statins was consistent across different risk groups (diabetes, chronic kidney disease, and ischemic heart disease). Conclusions: Statins with high cholesterol-lowering efficacy might increase the risk for developing severe renal failure. An alternative explanation is that the renal risk cannot be ameliorated as much as cardiovascular risk. Further follow-up studies or meta-analyses are needed to solve the controversy.
机译:背景:这项全国性的回顾性队列研究的目的是检查HMG-CoA还原酶抑制剂(他汀类药物)引发剂的肾脏预后。方法:从台湾国民健康保险索赔中确定2001年1月1日至2008年12月之间开始服用降胆固醇药(阿托伐他汀和罗舒伐他汀)和低效药物(洛伐他汀,辛伐他汀,普伐他汀和氟伐他汀)的他汀类药物的患者。数据库。感兴趣的结果是严重的肾衰竭,定义为血液透析,腹膜透析和肾脏移植的复合终点。应用比例风险回归模型来估计两组之间的发病率,并根据基线特征对倾向得分进行调整。结果:在26007和42249他汀类药物引发剂中,高效率组和低效率组的严重肾衰竭的发生率分别为每100人年0.65和0.46。尽管这两类人的心肌梗塞风险相当(危险比:1.06,95%CI:0.92-1.21),但在瑞舒伐他汀和阿托伐他汀引发剂中发生严重肾衰竭的危险增加了13%(危险比:1.13, 95%CI:1.02-1.26)。在不同风险组(糖尿病,慢性肾脏疾病和缺血性心脏病)中,这两种他汀类药物相关的风险增加是一致的。结论:具有降胆固醇作用的他汀类药物可能会增加发生严重肾衰竭的风险。另一种解释是,肾脏风险不能像心血管风险那样得到改善。需要进一步的随访研究或荟萃分析来解决这一争议。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号