In search of genes involved in neurodegenerative disorders

被引:21
作者
Pardo, LM [1 ]
van Duijn, CM [1 ]
机构
[1] Erasmus Univ, Dept Epidemiol & Biostat, Med Ctr, Genet Epidemiol Unit, NL-3000 DR Rotterdam, Netherlands
关键词
Alzheimer's disease; Parkinson's disease; genetics;
D O I
10.1016/j.mrfmmm.2005.06.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Dissecting the genetics of Alzheimer's disease (AD) and Parkinson's disease (PD) has contributed significantly to our understanding of the pathogenesis of neurodegeneration in these two complex disorders. For AD, three highly penetrant genes (amyloid precursor protein (APP, PSEN1 and PSEN2) and one susceptibility gene (APOE) have been identified. For PD. seven genes (SNCA, Parkin, UCHL1, NR4A2, DJ1, PINK1 and LRRK2) have been found. These genes explain only a small proportion of AD and PD patients and are mostly associated with an early onset presentation of the disease. APOE remains the only common gene, which increases the risk of both rare early and late onset AD. The ongoing challenge is to unravel the genetics of the most frequent forms of these complex disorders. In the present paper, we briefly review the state of the art in the genetics of AD and PD. We also discuss the prospects of finding new genes associated with common forms of these diseases in light of two hypotheses concerning the genetic variation of complex diseases: common disease/common variants and common disease/rare variants. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:89 / 101
页数:13
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