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Ezetimibe-simvastatin therapy reduce recurrent ischemic stroke risks in type 2 diabetic patients

  • Chi Hung Liu
  • , Tien Hsing Chen
  • , Ming Shyan Lin
  • , Ming Jui Hung
  • , Chang Ming Chung
  • , Wen-Chin Cherng
  • , Tsong Hai Lee
  • , Yu Sheng Lin*
  • *此作品的通信作者
  • Chang Gung University
  • Chang Gung Memorial Hospital

研究成果: 期刊稿件 › 文章 › 同行評審

19 引文 斯高帕斯(Scopus)

摘要

Context: Statin is the main lipid-lowering therapy for type 2 diabetes mellitus patients. Recent evidence suggested the cardiovascular protective effects of ezetimibe-simvastatin in acute coronary syndrome patients. Objective: To investigate the effect of ezetimibe-simvastatin combination therapy on stroke prevention among diabetic stroke patients. Design, Setting, Participants, andOutcomeMeasures: This is a retrospective cohort study. Between March 1, 2009 and December 31, 2011, all patients with type 2 diabetes mellitus in Taiwan's National Health Insurance Research Database were screened. Those admitted for ischemic stroke (IS) were recruited and divided into 10-mg ezetimibe-20-mg simvastatin (EZ-SIM), 40-mg atorvastatin (ATOR),and20-mgsimvastatin (SIM) groups for further analyses. The primary outcomeswere IS, myocardial infarction, and death from any cause. Patients were followed from index hospitalization to the date of death, loss of follow-up, or study termination. Results: During the 34-month follow-up period, the risk of recurrent IS in the SIM group was higher than that of the ATOR (hazard ratio [HR], 2.03;95%confidence interval [CI], 1.46-2.82) and EZ-SIM (HR, 1.69; 95% CI, 1.14-2.50) groups. The risk of recurrent IS was not significantly lower in the EZ-SIM compared with the ATOR group (HR, 1.20; 95% CI, 0.85-1.69). The incidence of composite endpoint was highest in the SIM group (28.2%), followed by the ATOR (16.1%) and EZ-SIM (15.4%) groups. The multivariate adjusted survival curve showed lower trends of recurrent IS in the EZ-SIM and ATOR groups compared with the SIM group. Conclusions: High-potency lipid-lowering therapy effectively reduces the risk of recurrent IS in diabetic patients regardless of ATOR or EZ-SIM combination therapy.

原文英語
頁(從 - 到)2994-3001
頁數8
期刊Journal of Clinical Endocrinology and Metabolism
卷101
發行號8
DOIs
出版狀態已出版 - 08 2016

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