Source:http://linkedlifedata.com/resource/pubmed/id/20473688
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-7-14
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pubmed:abstractText |
A recent pediatric-focused genome-wide association study has implicated three novel susceptibility loci for Crohn' disease (CD).We aimed to investigate whether the three recently reported and other previously reported genes/loci were also associated with CD in Canadian children. A case-control design was implemented at three pediatric gastroenterology clinics in Canada. Children <19 years of age with a confirmed diagnosis of CD were recruited along with controls. Single nucleotide polymorphisms (SNPs) in 19 reported genes/loci were genotyped. Associations between individual SNPs and CD were examined. A total of 563 cases and 553 controls were studied. The mean (+/-SD) age of the cases was 12.3 (+/-3.2) years. Most cases were male (56.0%), had ileo-colonic disease (L3 +/- L4, 48.8%) and inflammatory behavior (B1 +/- p, 87.9%) at diagnosis. Allelic association analysis (two-tailed) showed that 8 of the 19 targeted SNPs were significantly associated with overall susceptibility for CD. Associations with one additional SNP was borderline non-significant. Significantly associated SNPs included SNPs rs1250550 (p = 0.026) and rs8049439 (p = 0.04), recently reported to be specifically associated with pediatric-onset CD.Based on the results, we confirmed associations between two of the three novel pediatric-CD loci and other regions reported for associations with either pediatric and/or adult-onset CD.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1432-1203
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pubmed:author |
pubmed-author:AmreDevendra KDK,
pubmed-author:CosteaIrinaI,
pubmed-author:DeslandresColetteC,
pubmed-author:DongJinsongJ,
pubmed-author:FeguryHoudaH,
pubmed-author:GrimardGuyG,
pubmed-author:IsraelDavidD,
pubmed-author:KrupovesAlfredaA,
pubmed-author:LambrettePhlippeP,
pubmed-author:LevyEmileE,
pubmed-author:MackDavid RDR,
pubmed-author:MorganKennethK,
pubmed-author:OIMM,
pubmed-author:SeidmanErnest GEG
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pubmed:issnType |
Electronic
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pubmed:volume |
128
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
131-5
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pubmed:meshHeading |
pubmed-meshheading:20473688-Adult,
pubmed-meshheading:20473688-Alleles,
pubmed-meshheading:20473688-Canada,
pubmed-meshheading:20473688-Child,
pubmed-meshheading:20473688-Crohn Disease,
pubmed-meshheading:20473688-Genome,
pubmed-meshheading:20473688-Genome-Wide Association Study,
pubmed-meshheading:20473688-Genotype,
pubmed-meshheading:20473688-Humans,
pubmed-meshheading:20473688-Male,
pubmed-meshheading:20473688-Polymorphism, Single Nucleotide,
pubmed-meshheading:20473688-Research
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pubmed:year |
2010
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pubmed:articleTitle |
Association between genome-wide association studies reported SNPs and pediatric-onset Crohn's disease in Canadian children.
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pubmed:affiliation |
Department of Pediatrics, University of Montreal, Montreal, QC, Canada. devendra.amre@umontreal.ca
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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