ALZHEIMER'S DISEASE GENETICS: CURRENT STATUS AND FUTURE PERSPECTIVES

被引:51
作者
Bertram, Lars [1 ,2 ]
机构
[1] Max Planck Inst Mol Genet, Neuropsychiat Genet Grp, Dept Vertebrate Genom, D-14195 Berlin, Germany
[2] Massachusetts Gen Hosp, Dept Neurol, Genet & Aging Res Unit, Charlestown, MA 02129 USA
来源
NEUROBIOLOGY OF DEMENTIA | 2009年 / 84卷
关键词
GENOME-WIDE ASSOCIATION; NICOTINIC ACETYLCHOLINE-RECEPTORS; AMYLOID PRECURSOR PROTEIN; SYSTEMATIC METAANALYSES; MISSENSE MUTATIONS; APOLIPOPROTEIN-E; ONSET; SUSCEPTIBILITY; AGE; LINKAGE;
D O I
10.1016/S0074-7742(09)00409-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD) is a genetically complex disease whose pathogenesis is largely influenced by genetic factors. Three decades of intensive research have yielded four established AD genes (APP, PSEN1, PSEN2, APOE), and hundreds of potential susceptibility loci, none of which has been unequivocally shown to modify disease risk using conventional methodologies. The results of genome-wide association studies (GWAS) are now adding to an already vast and complicated body of data. To facilitate the evaluation and interpretation of these findings, we have recently created a database for genetic association studies in AD ("AlzGene"; available at http://www.alzgene.org). In addition to systematically screening and summarizing the scientific literature for eligible studies, AlzGene provides the results of allele-based meta-analyses for all polymorphisms with sufficient genotype data. Currently, these meta-analyses highlight over 20 different potential AD genes, several of which were originally implicated by a GWAS. First follow-up analyses in a large collection of over 1300 AD families reveal that-in addition to APOE-genetic variants in CHRNB2, GAB2, and TF show the most consistent risk effects across a wide range of independent samples and study designs. The chapter highlights these and other promising findings from the recent AD genetics literature and provides an overview of the powerful new tools aiding researchers today to unravel the genetic underpinnings of this devastating disease.
引用
收藏
页码:167 / 184
页数:18
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