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

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. M...

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Autores principales: Lehmann, Donald J, Barnardo, Martin CNM, Fuggle, Susan, Quiroga, Isabel, Sutherland, Andrew, Warden, Donald R, Barnetson, Lin, Horton, Roger, Beck, Stephan, Smith, A David
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764414/
https://www.ncbi.nlm.nih.gov/pubmed/17176470
http://dx.doi.org/10.1186/1742-2094-3-33
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author Lehmann, Donald J
Barnardo, Martin CNM
Fuggle, Susan
Quiroga, Isabel
Sutherland, Andrew
Warden, Donald R
Barnetson, Lin
Horton, Roger
Beck, Stephan
Smith, A David
author_facet Lehmann, Donald J
Barnardo, Martin CNM
Fuggle, Susan
Quiroga, Isabel
Sutherland, Andrew
Warden, Donald R
Barnetson, Lin
Horton, Roger
Beck, Stephan
Smith, A David
author_sort Lehmann, Donald J
collection PubMed
description 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 ε4 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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spelling pubmed-17644142007-01-06 Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity? Lehmann, Donald J Barnardo, Martin CNM Fuggle, Susan Quiroga, Isabel Sutherland, Andrew Warden, Donald R Barnetson, Lin Horton, Roger Beck, Stephan Smith, A David J Neuroinflammation Research 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 ε4 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. BioMed Central 2006-12-18 /pmc/articles/PMC1764414/ /pubmed/17176470 http://dx.doi.org/10.1186/1742-2094-3-33 Text en Copyright © 2006 Lehmann et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Lehmann, Donald J
Barnardo, Martin CNM
Fuggle, Susan
Quiroga, Isabel
Sutherland, Andrew
Warden, Donald R
Barnetson, Lin
Horton, Roger
Beck, Stephan
Smith, A David
Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity?
title Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity?
title_full Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity?
title_fullStr Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity?
title_full_unstemmed Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity?
title_short Replication of the association of HLA-B7 with Alzheimer's disease: a role for homozygosity?
title_sort replication of the association of hla-b7 with alzheimer's disease: a role for homozygosity?
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1764414/
https://www.ncbi.nlm.nih.gov/pubmed/17176470
http://dx.doi.org/10.1186/1742-2094-3-33
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