Protection against Alzheimer's Disease with APOE Christchurch Variant - How?

被引:0
|
作者
Hardy, John [1 ,2 ]
机构
[1] UCL, UK Dementia Res Inst, London, England
[2] UCL, Inst Neurol, Dept Neurodegenerat Dis, London, England
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2024年 / 390卷 / 23期
关键词
ONSET;
D O I
10.1056/NEJMe2403712
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Protective variants of genetic loci are of particular interest for two reasons: first, because they are important from a clinical genetic perspective; and second, because they may give mechanistic clues about potential therapeutic strategies. In Alzheimer's disease, the most prevalent protective allele is APOE2 (encoding apolipoprotein E2), which has a population allele frequency of approximately 10%.(1) With regard to the age at onset, sporadic Alzheimer's disease is delayed by approximately 10 years in persons with APOE2 homozygosity as compared with the general population.(2-4)APOE2 heterozygosity delays the onset of sporadic Alzheimer's disease by approximately 5 years (relative to APOE3 homozygosity) . . .
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页码:2212 / 2213
页数:2
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