The pursuit of susceptibility genes for Alzheimer's disease: progress and prospects

被引:82
作者
Sleegers, Kristel [1 ,2 ,3 ]
Lambert, Jean-Charles [4 ]
Bertram, Lars [5 ]
Cruts, Marc [1 ,2 ,3 ]
Amouyel, Philippe [4 ]
Van Broeckhoven, Christine [1 ,2 ,3 ]
机构
[1] VIB, Neurodegenerat Brain Dis Grp, Dept Mol Genet, B-2610 Antwerp, Belgium
[2] Inst Born Bunge, Neurogenet Lab, B-2610 Antwerp, Belgium
[3] Univ Antwerp, B-2610 Antwerp, Belgium
[4] Univ Lille Nord France, Inst Pasteur, INSERM, U744, F-59019 Lille, France
[5] Max Planck Inst Mol Genet, Dept Vertebrate Genom, Neuropsychiat Genet Grp, D-14195 Berlin, Germany
关键词
GENOME-WIDE ASSOCIATION; AMYLOID-BETA-PEPTIDE; CLATHRIN ASSEMBLY PROTEIN; CORONARY-HEART-DISEASE; COMPLEMENT-RECEPTOR; APOLIPOPROTEIN-E; MOUSE MODEL; IDENTIFIES VARIANTS; MISSENSE MUTATIONS; PLAQUE-FORMATION;
D O I
10.1016/j.tig.2009.12.004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The recent discoveries in genome-wide association studies (GWAS) of novel susceptibility loci (CLU, CR1 and PICALM) for Alzheimer's disease (AD) have elicited considerable interest in the AD community. But what are the implications of these purely epidemiological findings for our understanding of disease etiology and patient care? In this review, we attempt to place these findings in the context of current and future AD genetics research. CLU, CR1 and PICALM support existing hypotheses about the amyloid, lipid, chaperone and chronic inflammatory pathways in AD pathogenesis. We discuss how these and future findings can be translated into efforts to ameliorate patient care by genetic profiling for risk prediction and pharmacogenetics and by guiding drug development.
引用
收藏
页码:84 / 93
页数:10
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