Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1997-8-7
|
pubmed:abstractText |
Family and epidemiological studies support a genetic susceptibility to UC and CD. Conflicting reports regarding associations between UC and HLA-DR2 and between CD and various HLA alleles have been published. The aim of this study was to determine whether molecularly defined HLA-DR genes are associated with these diseases in a Dutch group of patients. Fifty-nine unrelated Dutch UC patients and 89 CD patients were typed using DNA-based methods. A total of 2400 healthy local blood donors served as controls. The phenotype frequency of the HLA-DRB1*15 allele was increased in UC patients compared with controls (42% versus 26% in controls; P = 0.006; odds ratio (OR) = 2.1), and was predominantly found in female patients (53% versus 24%; P = 0.001; OR = 3.5). The DRB1*15 allele was increased in UC patients having a positive family history (P = 0.01; OR = 5.8). Among the 16 patients who showed an increase in extent of disease during follow up, 10 were DRB1*15+ (P = 0.002; OR = 4.8). The frequency of the DRB1*13 allele was decreased in patients with UC (15% versus 28% in controls; P = 0.04; OR = 0.5). In CD, no association was observed between disease or particular clinical subgroups and any allele tested. The present study provides additional evidence for the genetic association between UC and HLA-DRB1*15, and supports recent findings that the susceptibility gene(s) for CD is not located in the HLA class II region.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0009-9104
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
109
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
175-9
|
pubmed:dateRevised |
2008-11-20
|
pubmed:meshHeading |
pubmed-meshheading:9218841-Adolescent,
pubmed-meshheading:9218841-Adult,
pubmed-meshheading:9218841-Aged,
pubmed-meshheading:9218841-Alleles,
pubmed-meshheading:9218841-Child,
pubmed-meshheading:9218841-Colitis, Ulcerative,
pubmed-meshheading:9218841-Crohn Disease,
pubmed-meshheading:9218841-DNA,
pubmed-meshheading:9218841-Female,
pubmed-meshheading:9218841-HLA-DR Antigens,
pubmed-meshheading:9218841-Humans,
pubmed-meshheading:9218841-Male,
pubmed-meshheading:9218841-Middle Aged,
pubmed-meshheading:9218841-Netherlands,
pubmed-meshheading:9218841-Polymerase Chain Reaction,
pubmed-meshheading:9218841-Prevalence,
pubmed-meshheading:9218841-Sex Factors
|
pubmed:year |
1997
|
pubmed:articleTitle |
Evidence for genetic heterogeneity in inflammatory bowel disease (IBD); HLA genes in the predisposition to suffer from ulcerative colitis (UC) and Crohn's disease (CD).
|
pubmed:affiliation |
Department of Gastroenterology, Academic Hospital Vrije Universiteit Amsterdam, The Netherlands.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|