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血管紧张素I转换酶基因的缺失等位基因作为认知障碍的遗传易感性因素。

The deletion allele of the angiotensin I converting enzyme gene as a genetic susceptibility factor for cognitive impairment.

作者信息

Amouyel P, Richard F, Cottel D, Amant C, Codron V, Helbecque N

机构信息

Service d'Epidémiologie et de Santé Publique, INSERM CJF 95-05, Institut Pasteur de Lille, France.

出版信息

Neurosci Lett. 1996 Oct 18;217(2-3):203-5.

PMID:8916108
Abstract

Experimental evidences suggest an implication of the renin angiotensin system (RAS) as a potential determinant of cognitive functions. To explore this hypothesis, we compared the distribution of an insertion (I)/deletion (D) polymorphism of the gene coding for the angiotensin I converting enzyme (ACE), a key enzyme of the RAS, in 228 elderly with cognitive impairment to that of 255 controls. The ACE D allele frequency was higher in the group with cognitive impairment (0.594) than in controls (0.514) (P < 0.02). The ACE DD genotype carriers had an increased risk of cognitive impairment (OR = 1.60, 95% CI (1.04-2.36), P < 0.03), independent of other risk factors of cognitive impairment: age, gender and presence of the apolipoprotein E epsilon 4 allele. This association was stronger in men (OR = 3.25, 95% CI (1.40-7.58), P < 0.006). This result suggests a possible implication of the RAS in human brain and cognitive functions.

摘要

实验证据表明肾素血管紧张素系统(RAS)可能是认知功能的一个潜在决定因素。为了探究这一假设,我们比较了228名认知功能受损老年人与255名对照组中,血管紧张素I转换酶(ACE)(RAS的关键酶)编码基因插入(I)/缺失(D)多态性的分布情况。认知功能受损组的ACE D等位基因频率(0.594)高于对照组(0.514)(P < 0.02)。ACE DD基因型携带者发生认知功能受损的风险增加(OR = 1.60,95% CI(1.04 - 2.36),P < 0.03),且独立于认知功能受损的其他风险因素:年龄、性别和载脂蛋白Eε4等位基因的存在。这种关联在男性中更强(OR = 3.25,95% CI(1.40 - 7.58),P < 0.006)。这一结果表明RAS可能与人脑及认知功能有关。

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