Smolders Barbara, Lemmens Robin, Thijs Vincent
Department of Clinical and Experimental Neurology, University Hospitals Leuven, Leuven, Belgium.
Stroke. 2007 Jun;38(6):1959-66. doi: 10.1161/STROKEAHA.106.480657. Epub 2007 May 3.
The relationship between elevated lipoprotein (a) levels[Lp(a)] and stroke is controversial. We systematically reviewed the literature to determine whether Lp(a) is a risk factor for stroke.
We searched MEDLINE (1966 to 2006), EMBASE (1974 to 2006), and Google scholar for articles on Lp(a) and cerebrovascular disease. From potentially relevant references retrieved, we excluded uncontrolled studies, studies of children with stroke, studies investigating carotid atherosclerosis, and studies lacking adequate data.
Thirty-one studies comprising 56 010 subjects with >4609 stroke events met all inclusion criteria and were included in the meta-analysis. In case-control studies (n=23 with 2600 strokes) unadjusted mean Lp(a) was higher in stroke patients (standardized mean difference, 0.39; 95% CI, 0.23 to 0.54) and was more frequently abnormally elevated (OR, 2.39; 95% CI, 1.57 to 3.63). Sensitivity analysis and meta-regression did not find any influence of study design, measurement period of Lp(a) in relationship to stroke episode, subtype, age, and sex to explain the substantial heterogeneity between studies (I(2)=83.7%; P<0.001). There was no evidence of publication bias. In nested case-control studies (n=3 with 364 strokes) Lp(a) was not a risk factor for incident stroke (OR, 1.04; 95% CI, 0.6 to 1.8). In prospective cohort studies (n=5 with >1645 strokes), incident stroke was more frequent in patients in the highest tertile of Lp(a) distribution compared with the lowest tertile of Lp(a) (RR, 1.22; 95% CI, 1.04 to 1.43). There was no publication bias or heterogeneity in the prospective studies (I(2)=0.00%; P=0.67).
This meta-analysis suggests that elevated Lp(a) is a risk factor for incident stroke.
脂蛋白(a)[Lp(a)]水平升高与中风之间的关系存在争议。我们系统回顾了文献,以确定Lp(a)是否为中风的危险因素。
我们检索了MEDLINE(1966年至2006年)、EMBASE(1974年至2006年)以及谷歌学术,查找关于Lp(a)和脑血管疾病的文章。从检索到的潜在相关参考文献中,我们排除了非对照研究、儿童中风研究、颈动脉粥样硬化研究以及缺乏足够数据的研究。
31项研究共纳入56010名受试者,其中有超过4609例中风事件,这些研究均符合所有纳入标准并被纳入荟萃分析。在病例对照研究(n = 23,共2600例中风)中,未调整的Lp(a)平均水平在中风患者中更高(标准化平均差,0.39;95%可信区间,0.23至0.54),且异常升高更为频繁(比值比,2.39;95%可信区间,1.57至3.63)。敏感性分析和荟萃回归未发现研究设计、Lp(a)与中风发作的测量时间、亚型、年龄和性别对解释研究之间的显著异质性(I² = 83.7%;P < 0.001)有任何影响。没有证据表明存在发表偏倚。在巢式病例对照研究(n = 3,共364例中风)中,Lp(a)不是新发中风的危险因素(比值比,1.04;95%可信区间,0.6至1.8)。在前瞻性队列研究(n = 5,超过1645例中风)中,与Lp(a)分布最低三分位数的患者相比,Lp(a)分布最高三分位数的患者中风发生率更高(风险比,1.22;95%可信区间,1.04至1.43)。前瞻性研究中没有发表偏倚或异质性(I² = 0.00%;P = 0.67)。
这项荟萃分析表明,Lp(a)升高是新发中风的危险因素。