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家族性高胆固醇血症与高低密度脂蛋白胆固醇血症与缺血性卒中的关系:哥本哈根普通人群研究。

Relationship of Familial Hypercholesterolemia and High Low-Density Lipoprotein Cholesterol to Ischemic Stroke: Copenhagen General Population Study.

机构信息

Department of Clinical Biochemistry (S.B., C.M.M., A.V., B.G.N).

Copenhagen General Population Study (S.B., C.M.M., A.V., M.B., B.G.N).

出版信息

Circulation. 2018 Aug 7;138(6):578-589. doi: 10.1161/CIRCULATIONAHA.118.033470.

Abstract

BACKGROUND

Familial hypercholesterolemia (FH) is a condition with very high concentrations of low-density lipoprotein (LDL) cholesterol and high risk of ischemic heart disease including myocardial infarction. However, there is limited and contradictory information on whether FH and high LDL cholesterol per se confer high risk of ischemic stroke. We tested the hypotheses that individuals in the general population with FH and/or high LDL cholesterol have higher risk of ischemic stroke.

METHODS

The associations of FH and high LDL cholesterol with ischemic stroke risk were tested in both causal, genetic, and observational analyses using 106 412 individuals from the CGPS (Copenhagen General Population Study; 2823 ischemic strokes and 3792 myocardial infarctions) and/or 10 372 individuals from the CCHS (Copenhagen City Heart Study; 945 ischemic strokes and 1142 myocardial infarctions). FH causative mutations were LDLR W23X(rs267607213), W66G(rs121908025) and W556S, and APOB R3500Q(rs5742904). A Mendelian randomization design tested whether high LDL cholesterol per se has a causal effect on ischemic stroke risk, using a combination of the FH causative mutations and common genetic variants associated with high LDL cholesterol.

RESULTS

The cumulative incidences in individuals in the CGPS with and without FH causative mutations were similar for ischemic stroke ( P=0.50) but not for myocardial infarction ( P<0.001): at age 80 years, 4% and 7% of these individuals developed ischemic stroke and 20% and 8% myocardial infarction, with similar results in the CCHS. There was no association between clinical FH and ischemic stroke, except if personal premature ischemic heart disease was included in the clinical FH criteria. Ischemic heart disease at baseline was associated with higher ischemic stroke risk, explaining the higher ischemic stroke risk in those with high LDL cholesterol. For a 1 mmol/L higher LDL cholesterol, the genetic causal risk ratio was 1.11 (0.62-2.02) for ischemic stroke and 1.45 (1.08-1.93) for myocardial infarction.

CONCLUSIONS

FH and high LDL cholesterol did not confer an increased risk of ischemic stroke. A positive association with ischemic stroke observed for some clinical FH criteria and high LDL cholesterol appears to be due to previous ischemic heart disease, rather than to high LDL cholesterol per se.

摘要

背景

家族性高胆固醇血症(FH)是一种 LDL 胆固醇浓度非常高且缺血性心脏病风险(包括心肌梗死)很高的病症。然而,关于 FH 和高 LDL 胆固醇本身是否会增加缺血性中风的风险,目前信息有限且存在争议。我们检验了以下假设:普通人群中患有 FH 和/或高 LDL 胆固醇的个体发生缺血性中风的风险更高。

方法

使用 CGPS(哥本哈根普通人群研究)中的 106412 名个体(2823 例缺血性中风和 3792 例心肌梗死)和/或 CCHS(哥本哈根城市心脏研究)中的 10372 名个体(945 例缺血性中风和 1142 例心肌梗死)进行因果、遗传和观察性分析,以检验 FH 和高 LDL 胆固醇与缺血性中风风险之间的关联。FH 的致病突变包括 LDLR W23X(rs267607213)、W66G(rs121908025)和 W556S 以及 APOB R3500Q(rs5742904)。孟德尔随机设计使用 FH 的致病突变和与高 LDL 胆固醇相关的常见遗传变异的组合,检验高 LDL 胆固醇本身是否对缺血性中风风险具有因果影响。

结果

CGPS 中患有 FH 致病突变和未患有 FH 致病突变的个体缺血性中风的累积发生率相似( P=0.50),但心肌梗死的发生率不同( P<0.001):在 80 岁时,这些个体中有 4%和 7%发生缺血性中风,20%和 8%发生心肌梗死,CCHS 中也有类似的结果。临床 FH 与缺血性中风之间没有关联,除非将个人的早发性缺血性心脏病纳入临床 FH 标准。基线时的缺血性心脏病与更高的缺血性中风风险相关,这解释了高 LDL 胆固醇患者中更高的缺血性中风风险。对于 LDL 胆固醇升高 1mmol/L,遗传因果风险比为缺血性中风 1.11(0.62-2.02)和心肌梗死 1.45(1.08-1.93)。

结论

FH 和高 LDL 胆固醇不会增加缺血性中风的风险。对于某些临床 FH 标准和高 LDL 胆固醇观察到的与缺血性中风呈正相关的情况,似乎是由于先前的缺血性心脏病,而不是高 LDL 胆固醇本身所致。

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