Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity?

被引:16
|
作者
Lehmann, Donald J. [1 ]
Barnardo, Martin C. N. M.
Fuggle, Susan
Quiroga, Isabel
Sutherland, Andrew
Warden, Donald R.
Barnetson, Lin
Horton, Roger
Beck, Stephan
Smith, A. David
机构
[1] Univ Dept Pharmacol, Oxford Project Invest Memory & Ageing OPTIMA, Oxford, England
[2] Radcliffe Infirm, Oxford OX2 6HE, England
[3] Univ Dept Physiol Anat & Genet, Oxford Ctr Gene Funct, Oxford OX1 3PT, England
[4] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg, Oxford OX3 9DU, England
[5] Churchill Hosp, Oxford Transplant Ctr, Oxford OX3 7LJ, England
[6] Wellcome Trust Sanger Inst, Immunogen Lab, Cambridge CB10 1SA, England
关键词
D O I
10.1186/1742-2094-3-33
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: There are reasons to expect an association with Alzheimer's disease (AD) within the HLA region. The HLA-B & C genes have, however, been relatively understudied. A geographically specific association with HLA-B7 & HLA-Cw*0702 had been suggested by our previous, small study. Methods: We studied the HLA-B & C alleles in 196 cases of 'definite' or 'probable' AD and 199 elderly controls of the OPTIMA cohort, the largest full study of these alleles in AD to date. Results: We replicated the association of HLA-B7 with AD (overall, adjusted odds ratio = 2.3, 95% confidence interval = 1.4-3.7, p = 0.001), but not the previously suggested interaction with the epsilon 4 allele of apolipoprotein E. Results for HLA-Cw*0702, which is in tight linkage disequilibrium with HLA-B7, were consistent with those for the latter. Homozygotes of both alleles appeared to be at particularly high risk of AD. Conclusion: HLA-B7 and HLA-Cw*0702 are associated with AD in the Oxford population. Because of the contradictions between cohorts in our previous study, we suggest that these results may be geographically specific. This might be because of differences between populations in the structure of linkage disequilibrium or in interactions with environmental, genetic or epigenetic factors. A much larger study will be needed to clarify the role of homozygosity of HLA alleles in AD risk.
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页数:7
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