Henyan Nickole N, Riche Daniel M, East Honey E, Gann Pamela N
School of Pharmacy, University of Mississippi, Jackson, MS, USA.
Ann Pharmacother. 2007 Dec;41(12):1937-45. doi: 10.1345/aph.1K280. Epub 2007 Nov 6.
Evidence from randomized, controlled trials suggests that reduction of low-density lipoprotein cholesterol with hydroxymethylglutaryl coenzyme A reductase inhibitor (statin) therapy in patients at high risk for cardiovascular disease reduces the incidence of ischemic stroke; however, data from large epidemiologic observational studies suggest an inverse relationship between risk of hemorrhagic stroke and cholesterol levels.
To perform a meta-analysis of randomized controlled trials to assess the effect of statin therapy on all cerebrovascular events (CVEs), ischemic stroke, and hemorrhagic stroke.
A systematic literature search of MEDLINE, EMBASE, Cumulative Index to Nursing & Allied Health Literature, and Web of Science citations from June 1975 through September 2006 was performed to identify randomized controlled trials of statin therapy. Trials were included if they met the following criteria: (1) controlled clinical trials of statin therapy versus placebo, (2) well-described protocol, and (3) data reported on incidence of all CVEs, ischemic stroke, or hemorrhagic stroke. All data were independently extracted by 3 investigators.
Weighted averages are reported as relative risk with 95% confidence intervals. A total of 26 trials (N = 100,560) reported incidence on all CVEs. Six trials (n = 37,292) reported incidence of ischemic stroke and 9 trials (n = 57,895) were included in the hemorrhagic stroke analysis. Statin therapy significantly reduced the risk of all CVEs (RR 0.83; 95% CI 0.76 to 0.91) and the risk of ischemic stroke (RR 0.79; 95% CI 0.63 to 0.99). Statin therapy did not significantly reduce risk of hemorrhagic stroke (RR 1.11; 95% CI 0.77 to 1.60).
Statin therapy significantly reduces risk of developing all CVEs and ischemic stroke; however, it is associated with a nonsignificant increase in risk of hemorrhagic stroke.
随机对照试验的证据表明,在心血管疾病高危患者中,使用羟甲基戊二酰辅酶A还原酶抑制剂(他汀类药物)治疗降低低密度脂蛋白胆固醇可降低缺血性卒中的发生率;然而,大型流行病学观察性研究的数据表明,出血性卒中风险与胆固醇水平呈负相关。
对随机对照试验进行荟萃分析,以评估他汀类药物治疗对所有脑血管事件(CVE)、缺血性卒中和出血性卒中的影响。
对1975年6月至2006年9月期间MEDLINE、EMBASE、护理学与健康相关文献累积索引以及科学引文索引中的文献进行系统检索,以确定他汀类药物治疗的随机对照试验。符合以下标准的试验纳入研究:(1)他汀类药物治疗与安慰剂对照的临床试验;(2)方案描述充分;(3)报告了所有CVE、缺血性卒中或出血性卒中发生率的数据。所有数据由3名研究人员独立提取。
加权平均值以相对风险及95%置信区间表示。共有26项试验(N = 100,560)报告了所有CVE的发生率。6项试验(n = 37,292)报告了缺血性卒中的发生率,9项试验(n = 57,895)纳入了出血性卒中分析。他汀类药物治疗显著降低了所有CVE的风险(RR 0.83;95% CI 0.76至0.91)以及缺血性卒中的风险(RR 0.79;95% CI 0.63至0.99)。他汀类药物治疗未显著降低出血性卒中的风险(RR 1.11;95% CI 0.77至1.60)。
他汀类药物治疗显著降低了发生所有CVE和缺血性卒中的风险;然而,它与出血性卒中风险的非显著增加相关。