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载脂蛋白E与阿尔茨海默病:基因型风险的种族差异

Apolipoprotein E and Alzheimer's disease: ethnic variation in genotypic risks.

作者信息

Maestre G, Ottman R, Stern Y, Gurland B, Chun M, Tang M X, Shelanski M, Tycko B, Mayeux R

机构信息

Center for Alzheimer's Disease Research, New York, NY.

出版信息

Ann Neurol. 1995 Feb;37(2):254-9. doi: 10.1002/ana.410370217.

Abstract

The presence of the apolipoprotein epsilon 4 (apo epsilon 4) allele significantly increases the risk of Alzheimer's disease. Whether this is due to biological effects of the apo epsilon 4 protein or reflects linkage disequilibrium with an as yet unidentified Alzheimer's disease susceptibility gene is of critical importance. In a community study in northern Manhattan we found a fivefold increase in the risk of Alzheimer's disease among African-Americans, Hispanics, and whites homozygous for apo epsilon 4. Overall, the risk between Alzheimer's disease and apo epsilon 4 heterozygosity was also increased by twofold, but the association was somewhat weaker for African-Americans than for Hispanics and whites. In contrast, the apo epsilon 2/epsilon 3 genotype was associated with an eightfold increased risk of Alzheimer's disease in African-Americans but it was associated with reduced risk in whites. Variability in the strength and type of association between Alzheimer's disease and the apo E polymorphisms in the three ethnic groups could not be fully explained by age differences. The allelic frequency of apo epsilon *4 was significantly higher in patients than control subjects in all ethnic groups at age 70 or younger, reflecting the higher proportion of apo epsilon 4 homozygotes, but this difference diminished with increasing age. The allelic frequency of apo epsilon *2 for African-Americans and Hispanics, but not whites, was significantly higher in patients than control subjects, but only after age 70.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

载脂蛋白ε4(apo ε4)等位基因的存在显著增加了患阿尔茨海默病的风险。这是由于apo ε4蛋白的生物学效应,还是反映了与尚未确定的阿尔茨海默病易感基因的连锁不平衡,至关重要。在曼哈顿北部的一项社区研究中,我们发现,apo ε4纯合的非裔美国人、西班牙裔人和白人患阿尔茨海默病的风险增加了五倍。总体而言,阿尔茨海默病与apo ε4杂合性之间的风险也增加了两倍,但非裔美国人的这种关联比西班牙裔人和白人稍弱。相比之下,apo ε2/ε3基因型与非裔美国人患阿尔茨海默病的风险增加八倍有关,但与白人的风险降低有关。三个种族群体中阿尔茨海默病与载脂蛋白E多态性之间关联的强度和类型差异,不能完全用年龄差异来解释。在70岁及以下的所有种族群体中,患者的apo ε4等位基因频率显著高于对照组,这反映了apo ε4纯合子的比例较高,但这种差异随着年龄的增长而减小。非裔美国人和西班牙裔人(而非白人)的apo ε2等位基因频率在患者中显著高于对照组,但仅在70岁以后。(摘要截选至250字)

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