Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9-10
pubmed:dateCreated
2001-1-26
pubmed:abstractText
Alzheimer's disease (AD) is a genetically complex and heterogeneous disorder. To date, a large number of candidate genes have been associated with the disease, however none of these findings has been consistently replicated in independent datasets. In this study we report the results of family-based analyses for polymorphisms of five such candidates on chromosomes 2 (interleukin-1beta, IL-1B), 3 (butyrylcholinesterase, BCHE), 11 (cathepsin D, CTSD; Fe65, APBB1) and 12 (lipoprotein receptor-related protein-1, LRP1) that were all suggested to be associated with AD in recent case-control studies. To minimize the possibility of spurious findings due to population admixture, we used a family-based design applying the sibship disequilibrium test (SDT) as well as two-point parametric linkage analyses on families from the National Institute of Mental Health (NIMH) Genetics Initiative. Contrary to the initial reports, none of the polymorphisms that were analyzed showed evidence for association or linkage with AD in our families. Our results suggest that the previously reported associations from case-control studies are either (a) false positive results, e.g. due to type I error or population admixture, (b) smaller than initially proposed, or (c) due to linkage disequilibrium with an as yet unidentified polymorphism nearby.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0531-5565
pubmed:author
pubmed:issnType
Print
pubmed:volume
35
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1353-61
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:11113613-Alleles, pubmed-meshheading:11113613-Alzheimer Disease, pubmed-meshheading:11113613-Apolipoproteins E, pubmed-meshheading:11113613-Butyrylcholinesterase, pubmed-meshheading:11113613-Cathepsin D, pubmed-meshheading:11113613-Family Health, pubmed-meshheading:11113613-Gene Frequency, pubmed-meshheading:11113613-Genes, pubmed-meshheading:11113613-Genotype, pubmed-meshheading:11113613-Humans, pubmed-meshheading:11113613-Interleukin-1, pubmed-meshheading:11113613-Linkage Disequilibrium, pubmed-meshheading:11113613-Low Density Lipoprotein Receptor-Related Protein-1, pubmed-meshheading:11113613-Nerve Tissue Proteins, pubmed-meshheading:11113613-Nuclear Family, pubmed-meshheading:11113613-Nuclear Proteins, pubmed-meshheading:11113613-Polymorphism, Genetic, pubmed-meshheading:11113613-Receptors, Immunologic, pubmed-meshheading:11113613-Statistics, Nonparametric
pubmed:year
2000
pubmed:articleTitle
Candidate genes showing no evidence for association or linkage with Alzheimer's disease using family-based methodologies.
pubmed:affiliation
Genetics and Aging Unit, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't