Source:http://linkedlifedata.com/resource/pubmed/id/17066478
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2007-3-1
|
pubmed:abstractText |
Based on the dopaminergic hypothesis, the dopamine D(1) receptor gene (DRD1) is considered to be a good candidate gene involved in the susceptibility of bipolar disorder (BP). Genetic association between three DRD1 single nucleotide polymorphisms (SNPs) (-800T/C, -48A/G, and 1403T/C) and bipolar type I (BP I) disorder was performed in a case-control sample of Sardinian origin (170 BP I and 209 controls) and in an enlarged sample (229 families) of BP I trios from Toronto. The haplotype analyses generated significant global chi-square in both samples (P-value 0.024 in Toronto and 0.00042 in Sardinian). The main representative haplotypes in both samples were the -800T/-48A/1403C and the -800C/-48G/1403T. Considering each group individually, the -800C/-48G/1403T was transmitted more frequently from parents to BP I probands in Toronto sample (nominally P-value = 0.047) and was more frequent in cases than in control subjects in Sardinian sample although showing no significant evidence of association (nominally P-value = 0.16) When the estimated haplotype counts of both samples were combined, the global chi(2) was significant (P-value = 0.00085) and the nominal P-value for the haplotype -800C/-48G/1403T was 0.01. The fact that the same haplotype shows a similar trend for association in samples originating from different ethnic backgrounds seems to imply that the -800C/-48G/1403T haplotype may be considered as a risk factor for BP I disorder.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
1552-4841
|
pubmed:author | |
pubmed:copyrightInfo |
(c) 2007 Wiley-Liss, Inc.
|
pubmed:issnType |
Print
|
pubmed:day |
5
|
pubmed:volume |
144B
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
237-41
|
pubmed:dateRevised |
2008-5-21
|
pubmed:meshHeading |
pubmed-meshheading:17066478-Adult,
pubmed-meshheading:17066478-Alleles,
pubmed-meshheading:17066478-Bipolar Disorder,
pubmed-meshheading:17066478-Canada,
pubmed-meshheading:17066478-Case-Control Studies,
pubmed-meshheading:17066478-Female,
pubmed-meshheading:17066478-Genetic Predisposition to Disease,
pubmed-meshheading:17066478-Haplotypes,
pubmed-meshheading:17066478-Humans,
pubmed-meshheading:17066478-Italy,
pubmed-meshheading:17066478-Male,
pubmed-meshheading:17066478-Polymorphism, Single Nucleotide,
pubmed-meshheading:17066478-Receptors, Dopamine D1,
pubmed-meshheading:17066478-Risk Factors
|
pubmed:year |
2007
|
pubmed:articleTitle |
Haplotype association study between DRD1 gene and bipolar type I affective disorder in two samples from Canada and Sardinia.
|
pubmed:affiliation |
Department of Neurosciences B.B. Brodie, Section of Clinical Pharmacology, Center of Clinical Psychopharmacology, University of Cagliari, Cagliari, Italy. delzompo@unica.it
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|