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Association study of cholesterol-related genes in Alzheimer's disease

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dc.contributor.author Wollmer, MA en
dc.contributor.author Sleegers, K en
dc.contributor.author Ingelsson, M en
dc.contributor.author Zekanowski, C en
dc.contributor.author Brouwers, N en
dc.contributor.author Maruszak, A en
dc.contributor.author Brunner, F en
dc.contributor.author Huynh, KD en
dc.contributor.author Kilander, L en
dc.contributor.author Brundin, RM en
dc.contributor.author Hedlund, M en
dc.contributor.author Giedraitis, V en
dc.contributor.author Glaser, A en
dc.contributor.author Engelborghs, S en
dc.contributor.author De Deyn, PP en
dc.contributor.author Kapaki, E en
dc.contributor.author Tsolaki, M en
dc.contributor.author Daniilidou, M en
dc.contributor.author Molyva, D en
dc.contributor.author Paraskevas, GP en
dc.contributor.author Thal, DR en
dc.contributor.author Barcikowska, M en
dc.contributor.author Kuznicki, J en
dc.contributor.author Lannfelt, L en
dc.contributor.author Van Broeckhoven, C en
dc.contributor.author Nitsch, RM en
dc.contributor.author Hock, C en
dc.contributor.author Papassotiropoulos, A en
dc.date.accessioned 2014-03-01T01:56:28Z
dc.date.available 2014-03-01T01:56:28Z
dc.date.issued 2007 en
dc.identifier.issn 1364-6745 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/28106
dc.subject HMGCS2 en
dc.subject FDPS en
dc.subject NPC2 en
dc.subject ABCG1 en
dc.subject polymorphism en
dc.subject.classification Genetics & Heredity en
dc.subject.classification Clinical Neurology en
dc.subject.other LATE-ONSET en
dc.subject.other APOLIPOPROTEIN-E en
dc.subject.other RISK-FACTOR en
dc.subject.other GENOME SCREEN en
dc.subject.other AMYLOID LOAD en
dc.subject.other METABOLISM en
dc.subject.other CHROMOSOME-10 en
dc.subject.other LINKAGE en
dc.subject.other ALLELE en
dc.subject.other SUSCEPTIBILITY en
dc.title Association study of cholesterol-related genes in Alzheimer's disease en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2007 en
heal.abstract Alzheimer's disease (AD) is a genetically complex disorder, and several genes related to cholesterol metabolism have been reported to contribute to AD risk. To identify further AD susceptibility genes, we have screened genes that map to chromosomal regions with high logarithm of the odds scores for AD in full genome scans and are related to cholesterol metabolism. In a European screening sample of 115 sporadic AD patients and 191 healthy control subjects, we analyzed single nucleotide polymorphisms in 28 cholesterol-related genes for association with AD. The genes HMGCS2, FDPS, RAFTLIN, ACAD8, NPC2, and ABCG1 were associated with AD at a significance level of P <= 0.05 in this sample. Replication trials in five independent European samples detected associations of variants within HMGCS2, FDPS, NPC2, or ABCG1 with AD in some samples (P=0.05 to P=0.005). We did not identify a marker that was significantly associated with AD in the pooled sample (n=2864). Stratification of this sample revealed an APOE-dependent association of HMGCS2 with AD (P=0.004). We conclude that genetic variants investigated in this study may be associated with a moderate modification of the risk for AD in some samples. en
heal.publisher SPRINGER en
heal.journalName NEUROGENETICS en
dc.identifier.isi ISI:000247971400003 en
dc.identifier.volume 8 en
dc.identifier.issue 3 en
dc.identifier.spage 179 en
dc.identifier.epage 188 en


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