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dc.contributor.authorFukumoto, N
dc.contributor.authorFujii, T
dc.contributor.authorCombarros, O
dc.contributor.authorKamboh, MI
dc.contributor.authorTsai, S-J
dc.contributor.authorMatsushita, S
dc.contributor.authorNacmias, B
dc.contributor.authorComings, DE
dc.contributor.authorArboleda, H
dc.contributor.authorIngelsson, M
dc.contributor.authorHyman, BT
dc.contributor.authorAkatsu, H
dc.contributor.authorGrupe, A
dc.contributor.authorNishimura, AL
dc.contributor.authorZatz, M
dc.contributor.authorMattila, KM
dc.contributor.authorRinne, J
dc.contributor.authorGoto, Y-I
dc.contributor.authorAsada, T
dc.contributor.authorNakamura, S
dc.contributor.authorKunugi, H
dc.date.accessioned2024-01-03T14:38:34Z
dc.date.available2024-01-03T14:38:34Z
dc.date.issued2010-01
dc.identifier.citationFukumoto N, Fujii T, Combarros O, Kamboh MI, Tsai S-J, Matsushita S, Nacmias B, Comings DE, Arboleda H, Ingelsson M, Hyman BT, Akatsu H, Grupe A, Nishimura AL, Zatz M, Mattila KM, Rinne J, Goto Y, Asada T, Nakamura S, Kunugi H. 2010. Sexually Dimorphic Effect of the Val66Met Polymorphism of BDNF on Susceptibility to Alzheimer's Disease: New Data and Meta-Analysis. Am J Med Genet Part B 153B:235–242.en_US
dc.identifier.issn1552-4841
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/93338
dc.description.abstractConflicting results have been reported as to whether genetic variations (Val66Met and C270T) of the brain-derived neurotrophic factor gene (BDNF) confer susceptibility to Alzheimer's disease (AD). We genotyped these polymorphisms in a Japanese sample of 657 patients with AD and 525 controls, and obtained weak evidence of association for Val66Met (P = 0.063), but not for C270T. After stratification by sex, we found a significant allelic association between Val66Met and AD in women (P = 0.017), but not in men. To confirm these observations, we collected genotyping data for each sex from 16 research centers worldwide (4,711 patients and 4,537 controls in total). The meta-analysis revealed that there was a clear sex difference in the allelic association; the Met66 allele confers susceptibility to AD in women (odds ratio = 1.14, 95% CI 1.05-1.24, P = 0.002), but not in men. Our results provide evidence that the Met66 allele of BDNF has a sexually dimorphic effect on susceptibility to AD.en_US
dc.format.extent235 - 242
dc.languageeng
dc.language.isoenen_US
dc.publisherWileyen_US
dc.relation.ispartofAmerican Journal of Medical Genetics Part B: Neuropsychiatric Genetics
dc.subjectAgeden_US
dc.subjectAlzheimer Diseaseen_US
dc.subjectBase Sequenceen_US
dc.subjectBrain-Derived Neurotrophic Factoren_US
dc.subjectCase-Control Studiesen_US
dc.subjectDNA Primersen_US
dc.subjectFemaleen_US
dc.subjectGenetic Predisposition to Diseaseen_US
dc.subjectHumansen_US
dc.subjectMaleen_US
dc.subjectMethionineen_US
dc.subjectSex Characteristicsen_US
dc.subjectValineen_US
dc.titleSexually dimorphic effect of the Val66Met polymorphism of BDNF on susceptibility to Alzheimer's disease: New data and meta-analysis.en_US
dc.typeArticleen_US
dc.rights.holderCopyright © 2009 Wiley-Liss, Inc.
dc.identifier.doi10.1002/ajmg.b.30986
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/19504537en_US
pubs.issue1en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.publisher-urlhttp://doi.org/10.1002/ajmg.b.30986
pubs.volume153Ben_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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