Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2011-3-17
pubmed:abstractText
Rare mutations in PARK loci genes cause Parkinson's disease (PD) in some families and isolated populations. We investigated the association of common variants in PARK loci and related genes with PD susceptibility and age at onset in an outbred population. A total of 1,103 PD cases from the upper Midwest, USA, were individually matched to unaffected siblings (n = 654) or unrelated controls (n = 449) from the same region. Using a sequencing approach in 25 cases and 25 controls, single nucleotide polymorphisms (SNPs) in species-conserved regions of PARK loci and related genes were detected. We selected additional tag SNPs from the HapMap. We genotyped a total of 235 SNPs and two variable number tandem repeats in the ATP13A2, DJ1, LRRK1, LRRK2, MAPT, Omi/HtrA2, PARK2, PINK1, SNCA, SNCB, SNCG, SPR, and UCHL1 genes in all 2,206 subjects. Case-control analyses were performed to study association with PD susceptibility, while cases-only analyses were used to study association with age at onset. Only MAPT SNP rs2435200 was associated with PD susceptibility after correction for multiple testing (OR = 0.74, 95% CI = 0.64-0.86, uncorrected P < 0.0001, log additive model); however, 16 additional MAPT variants, seven SNCA variants, and one LRRK2, PARK2, and UCHL1 variants each had significant uncorrected P-values. There were no significant associations for age at onset after correction for multiple testing. Our results confirm the association of MAPT and SNCA genes with PD susceptibility but show limited association of other PARK loci and related genes with PD.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1531-8257
pubmed:author
pubmed:copyrightInfo
Copyright © 2010 Movement Disorder Society.
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
280-8
pubmed:meshHeading
pubmed-meshheading:21412835-Age of Onset, pubmed-meshheading:21412835-Aged, pubmed-meshheading:21412835-Aged, 80 and over, pubmed-meshheading:21412835-Case-Control Studies, pubmed-meshheading:21412835-Female, pubmed-meshheading:21412835-Genetic Association Studies, pubmed-meshheading:21412835-Genetic Loci, pubmed-meshheading:21412835-Genetic Predisposition to Disease, pubmed-meshheading:21412835-Genetic Variation, pubmed-meshheading:21412835-Genotype, pubmed-meshheading:21412835-Haplotypes, pubmed-meshheading:21412835-Humans, pubmed-meshheading:21412835-Male, pubmed-meshheading:21412835-Odds Ratio, pubmed-meshheading:21412835-Parkinson Disease, pubmed-meshheading:21412835-Polymorphism, Single Nucleotide, pubmed-meshheading:21412835-Ubiquitin-Protein Ligases, pubmed-meshheading:21412835-alpha-Synuclein, pubmed-meshheading:21412835-tau Proteins
pubmed:year
2011
pubmed:articleTitle
Common variants in PARK loci and related genes and Parkinson's disease.
pubmed:affiliation
Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural