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载脂蛋白E ε4等位基因作为散发性早发型和晚发型阿尔茨海默病的主要危险因素:19q13.2染色体区域分析

Apolipoprotein E, epsilon 4 allele as a major risk factor for sporadic early and late-onset forms of Alzheimer's disease: analysis of the 19q13.2 chromosomal region.

作者信息

Chartier-Harlin M C, Parfitt M, Legrain S, Pérez-Tur J, Brousseau T, Evans A, Berr C, Vidal O, Roques P, Gourlet V

机构信息

INSERM U156, Laboratoire de Neurosciences, Lille, France.

出版信息

Hum Mol Genet. 1994 Apr;3(4):569-74. doi: 10.1093/hmg/3.4.569.

Abstract

An association between the 19q13.2 chromosomal region and Alzheimer's disease (AD) has been reported in AD families and for sporadic AD. Recent observations provide evidence that the epsilon 4 allele of the apolipoprotein E gene (APOE), located in this region, is a risk factor for late-onset AD. Within this region, other genes possibly involved in the pathophysiology of AD and in strong linkage disequilibrium with the APOE locus may be responsible for this association. To test this hypothesis, we analysed the allelic distribution of four polymorphic genetic markers flanking the APOE gene (D19S178 (CA)n repeat, D19S47 (CA)n repeat, APOCI HpaI restriction fragment length polymorphism, APOCII (CA)n repeat). We performed these analyses in a sample of late-onset sporadic cases (n = 36) versus controls (n = 38), and in a sample of early-onset sporadic cases (n = 34) versus controls (n = 36). Early-onset cases were analysed for two cut-offs with late-onset: less than 60 and less than 65. We observed a significant increased frequency of the APOE epsilon 4 allele in late-onset and early-onset AD with ages at onset less than 60 and less than 65. The adjusted odds ratio (OR) of the bearers of at least one APOE epsilon 4 allele was 4.10 ([1.84;9.16]) when estimated in both populations with a logistic regression model. Surprisingly, the odds ratio of the bearers of at least one APOE epsilon 2 allele was also significant and equal to 0.11 ([0.02;0.50]) suggesting a possible protective effect.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在阿尔茨海默病(AD)家族及散发性AD病例中,均有报道称19号染色体13.2区域与AD存在关联。近期观察结果表明,位于该区域的载脂蛋白E基因(APOE)的ε4等位基因是晚发型AD的一个风险因素。在这个区域内,其他可能参与AD病理生理过程且与APOE基因座存在强连锁不平衡的基因,可能是这种关联的原因。为验证这一假设,我们分析了APOE基因侧翼的四个多态性遗传标记的等位基因分布(D19S178(CA)n重复序列、D19S47(CA)n重复序列、APOCI HpaI限制性片段长度多态性、APOCII(CA)n重复序列)。我们在晚发型散发病例样本(n = 36)与对照样本(n = 38),以及早发型散发病例样本(n = 34)与对照样本(n = 36)中进行了这些分析。早发型病例根据发病年龄与晚发型的两个分界点进行分析:小于60岁和小于65岁。我们观察到,发病年龄小于60岁和小于65岁的晚发型和早发型AD中,APOE ε4等位基因的频率显著增加。在两个群体中用逻辑回归模型估计时,至少携带一个APOE ε4等位基因者的校正优势比(OR)为4.10([1.84;9.16])。令人惊讶的是,至少携带一个APOE ε2等位基因者的优势比也具有显著性,等于0.11([0.02;0.50]),提示可能存在保护作用。(摘要截选至250词)

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