Genetics of Alzheimer's disease

被引:11
|
作者
Seto-Salvia, Nuria [1 ,2 ]
Clarimon, Jordi [1 ]
机构
[1] Hosp Santa Creu & Sant Pau, Lab Alzheimer, Ctr Invest Biomed & Red Enfermedades Neurodegener, E-08025 Barcelona, Spain
[2] Univ Rovira & Virgili IPHES, Grp Autoecol Humana Cuaternario, Tarragona, Spain
关键词
Alzheimer; Amyloid; APOE; Genetics; Genome-wide association studies; Presenilins; GENOME-WIDE ASSOCIATION; APOLIPOPROTEIN-E; IDENTIFIES VARIANTS; TYPE-4; ALLELE; SUSCEPTIBILITY; RISK; EPSILON-4; DEMENTIA; GENES; APOE;
D O I
10.33588/rn.5006.2010033
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction and development. Alzheimer's disease (AD), the leading cause of dementia, is a complex disorder in which genetic and environmental factors interact. Three genes -the amyloid precursor protein (APP) and the presenilin 1 and 2 (PSEN1 and PSEN2)-have been linked to atusosomal dominant forms of AD. Besides, a fourth gene -the apolipoprotein E gene (APOE)-seems to be the only major genetic factor related to late-onset sporadic and familial AD cases. Although more than a thousand studies have been performed to date, little is known about other genetic factors leading to this devastating dementia. Nevertheless, the last three years have witnessed a surge in genetic research of AD due to the implementation of novel technologies enabling large-scale genetic analyses. Conclusion. This review provides a summary of current knowledge about AD in the genetic field.
引用
收藏
页码:360 / 364
页数:5
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