HLA class I, II & III genes in confirmed late-onset Alzheimer's disease

被引:26
作者
Lehmann, DJ
Wiebusch, H
Marshall, SE
Johnston, C
Warden, DR
Morgan, K
Schappert, K
Poirier, J
Xuereb, J
Kalsheker, N
Welsh, KI
Smith, AD
机构
[1] Univ Oxford, Dept Pharmacol, Oxford Project Investigate Memory & Ageing, OPTIMA, Oxford OX1 3QT, England
[2] Nova Mol Inc, Montreal, PQ H4A 3S5, Canada
[3] Churchill Hosp, Oxford Transplant Ctr, Nuffield Dept Surg, Oxford OX3 7LJ, England
[4] Univ Nottingham, Queens Med Ctr, Sch Clin Lab Sci, Div Clin Chem, Nottingham NG7 2UH, England
[5] Univ Cambridge, Sch Clin, Addenbrookes Hosp, Dept Histopathol, Cambridge CB2 2QH, England
关键词
allele; risk; apolipoprotein E; butyrylcholinesterase; tumor necrosis factor; lymphotoxin alpha; heat shock protein;
D O I
10.1016/S0197-4580(00)00180-9
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
We first examined all the then known alleles (1997) at the HLA-A, B, Bw, C, DRB1, 3, 4 and 5, and DQB1 loci in 55 late-onset (>65y) AD eases and 73 elderly controls from Oxford. We found an association of HLA-B7 with late-onset AD (odds ratio = 3.1, corrected P = 0.04) that was limited to apolipoprotein E epsilon4-negative subjects (odds ratio = 5.1, corrected P = 0.005). We then studied linkages with Class III genes and, finally, we sought to replicate our HLA-B7 result in cohorts from Montreal and Nottingham. Altogether, we used 299 histopathologically confirmed cases of late-onset AD and 175 controls. Our initial, clear finding was not replicated in Montreal and Nottingham, however. We also failed to support any other previously reported association of AD with an HLA gene. Though we cannot exclude distinct linkages in different cohorts as an explanation of the conflicting results of HLNAD studies, we conclude that there is no compelling evidence of a strong, direct association between late-onset AD and any HLA Class I or II allele. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:71 / 77
页数:7
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