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BDNF 196 G/A and 270 C/T Polymorphisms and Susceptibility to Parkinson's Disease: A Meta-Analysis

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dc.contributor.authorLee, Young Ho-
dc.contributor.authorSong, Gwan Gyu-
dc.date.accessioned2021-09-05T12:29:13Z-
dc.date.available2021-09-05T12:29:13Z-
dc.date.created2021-06-15-
dc.date.issued2014-01-01-
dc.identifier.issn0022-2895-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/99581-
dc.description.abstractThe aim of this study was to explore whether brain-derived neurotrophic factor (BDNF) polymorphisms 196G/A and 270 C/T confer susceptibility to Parkinson's disease (PD). The authors conducted a meta-analysis of the associations between the BDNF 196G/A and 270 C/T polymorphisms and PD in subjects. They considered 12 studies in the case of the BDNF 196G/A polymorphism and 4 studies in the case of the BDNF 270 C/T polymorphism. Meta-analysis showed no association between PD and the BDNF 196A allele in all study subjects (odds ratio [OR] = 1.066, 95% CI [0.972, 1.169], p = .173). However, ethnicity-specific meta-analysis identified an association between the BDNF 196 AA + AG genotype and PD in Europeans, but not in Asians (OR = 1.212, 95% CI [1.007, 1.458], p = .042; OR = 1.0567, 95% CI [0.913, 1.221], p = .465). Meta-analysis showed no association between PD and the BDNF 270 C/T polymorphism (OR for the T allele = 1.213, 95% CI [0.923, 1.595], p = .165). This meta-analysis identified an association between the BDNF 196G/A polymorphism in Europeans, but not in Asians, but failed to identify an association between the BDNF 270 C/T polymorphism and PD.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherROUTLEDGE JOURNALS, TAYLOR & FRANCIS LTD-
dc.subjectNEUROTROPHIC FACTOR GENE-
dc.subjectSYSTEMIC-LUPUS-ERYTHEMATOSUS-
dc.subjectVAL66MET POLYMORPHISM-
dc.subjectALZHEIMERS-DISEASE-
dc.subjectG196A POLYMORPHISM-
dc.subjectHUMAN BRAIN-
dc.subjectASSOCIATION-
dc.subjectONSET-
dc.subjectAGE-
dc.subjectSECRETION-
dc.titleBDNF 196 G/A and 270 C/T Polymorphisms and Susceptibility to Parkinson's Disease: A Meta-Analysis-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Young Ho-
dc.contributor.affiliatedAuthorSong, Gwan Gyu-
dc.identifier.doi10.1080/00222895.2013.862199-
dc.identifier.scopusid2-s2.0-84891626898-
dc.identifier.wosid000329140000007-
dc.identifier.bibliographicCitationJOURNAL OF MOTOR BEHAVIOR, v.46, no.1, pp.59 - 66-
dc.relation.isPartOfJOURNAL OF MOTOR BEHAVIOR-
dc.citation.titleJOURNAL OF MOTOR BEHAVIOR-
dc.citation.volume46-
dc.citation.number1-
dc.citation.startPage59-
dc.citation.endPage66-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassssci-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaPsychology-
dc.relation.journalResearchAreaSport Sciences-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.relation.journalWebOfScienceCategoryPsychology-
dc.relation.journalWebOfScienceCategoryPsychology, Experimental-
dc.relation.journalWebOfScienceCategorySport Sciences-
dc.subject.keywordPlusNEUROTROPHIC FACTOR GENE-
dc.subject.keywordPlusSYSTEMIC-LUPUS-ERYTHEMATOSUS-
dc.subject.keywordPlusVAL66MET POLYMORPHISM-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusG196A POLYMORPHISM-
dc.subject.keywordPlusHUMAN BRAIN-
dc.subject.keywordPlusASSOCIATION-
dc.subject.keywordPlusONSET-
dc.subject.keywordPlusAGE-
dc.subject.keywordPlusSECRETION-
dc.subject.keywordAuthorbrain-derived neurotrophic factor-
dc.subject.keywordAuthormeta-analysis-
dc.subject.keywordAuthorParkinson&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorpolymorphism-
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