The genetic risk of Alzheimer's disease beyond APOE ε4: systematic review of Alzheimer's genetic risk scores

被引:72
作者
Stocker, Hannah [1 ,2 ,3 ]
Moellers, Tobias [1 ,2 ,3 ]
Perna, Laura [2 ]
Brenner, Hermann [1 ,2 ]
机构
[1] Heidelberg Univ, Network Aging Res, Bergheimer Str 20, D-69115 Heidelberg, Germany
[2] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, Neuenheimer Feld 581, D-69120 Heidelberg, Germany
[3] Heidelberg Univ, Med Fac, D-69120 Heidelberg, Germany
关键词
ASSOCIATION; DEMENTIA; LOCI; PREDICTION; BIOMARKERS; VARIANTS; REVEALS;
D O I
10.1038/s41398-018-0221-8
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
The epsilon 4 allele of Apolipoprotein E (APOE) is the strongest known genetic risk factor of Alzheimer's disease (AD) but does not account for the entirety of genetic risk. Genetic risk scores (GRSs) incorporating additional genetic variants have been developed to determine the genetic risk for AD, yet there is no systematic review assessing the contribution of GRSs for AD beyond the effect of APOE epsilon 4. The purpose of this systematic PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-analyses)-based review was to summarize original research studies that have developed and validated a GRS for AD utilizing associated single nucleotide polymorphisms (SNPs). The PubMed and Web of Science databases were searched on April 6, 2018 and screening was completed on 2018 citations by two independent reviewers. Eighteen studies published between 2010 and 2018 were included in the review. All GRSs expressed significant associations or discrimination capability of AD when compared to clinically normal controls; however, GRS prediction of MCI to AD conversion was mixed. APOE epsilon 4 status was more predictive of AD than the GRSs, although the GRSs did add to AD prediction accuracy beyond APOE epsilon 4. GRSs might contribute to identifying genetic risk of AD beyond APOE. However, additional studies are warranted to assess the performance of GRSs in independent longitudinal cohorts.
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页数:9
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