Source:http://linkedlifedata.com/resource/pubmed/id/12500190
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2002-12-24
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pubmed:abstractText |
Hepatitis C virus (HCV) infection is a major risk factor for developing hepatocellular carcinoma (HCC), a life-threatening sequel. However, the factors that affect disease progression to HCC have not been thoroughly elucidated. Genetic polymorphisms in proinflammatory cytokines, the interleukin 1 (IL-1) family (IL-1beta and IL-1ra) and tumor necrosis factor-alpha (TNF-alpha), were studied in 274 Japanese patients with chronic HCV infection and 55 healthy individuals using standard polymerase chain reaction-based genotyping techniques. The association between these polymorphisms and disease status was evaluated while controlling for confounding clinical variables. The proportion of patients with HCC in the IL-1beta-31 T/T (55%, odds ratio to C/C was 2.63, P =.009) genotype was higher than in the T/C (44%, odds ratio to C/C was 1.64, P =.149) and C/C genotypes (35%). The IL-1beta-31 and -511 loci were in near complete linkage disequilibrium, and the IL-1beta-511/-31 haplotype C-T was significantly associated with the presence of HCC (odds ratio of 1.51, P =.02). Polymorphisms in the TNF-alpha gene were not associated with disease. A multivariate analysis revealed that the IL-1beta-31 T/T genotype, alpha-fetoprotein >20 microg/L, presence of cirrhosis, male sex, and age >60 years were associated with the presence of HCC at odds ratios of 3.73 (T/T vs. C/C), 4.12, 4.03, 3.89, and 3.27, respectively. In conclusion, the IL-1beta-31 genotype T/T or the IL-1beta-511/-31 haplotype C-T is associated with the presence of HCC in Japanese patients with chronic HCV infection.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0270-9139
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pubmed:author |
pubmed-author:GotoTadashiT,
pubmed-author:HoshidaYujinY,
pubmed-author:ItoYoichiY,
pubmed-author:KatoNaoyaN,
pubmed-author:MoriyamaMasaruM,
pubmed-author:OmataMasaoM,
pubmed-author:OtsukaMotoyukiM,
pubmed-author:ShiinaShuichiroS,
pubmed-author:ShiratoriYasushiY,
pubmed-author:TaniguchiHiroyoshiH,
pubmed-author:WangYueY,
pubmed-author:YoshidaHideoH
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pubmed:issnType |
Print
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pubmed:volume |
37
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
65-71
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12500190-Adult,
pubmed-meshheading:12500190-Aged,
pubmed-meshheading:12500190-Carcinoma, Hepatocellular,
pubmed-meshheading:12500190-Female,
pubmed-meshheading:12500190-Genetic Predisposition to Disease,
pubmed-meshheading:12500190-Genotype,
pubmed-meshheading:12500190-Hepatitis C, Chronic,
pubmed-meshheading:12500190-Humans,
pubmed-meshheading:12500190-Interleukin-1,
pubmed-meshheading:12500190-Liver Neoplasms,
pubmed-meshheading:12500190-Male,
pubmed-meshheading:12500190-Middle Aged,
pubmed-meshheading:12500190-Polymorphism, Genetic,
pubmed-meshheading:12500190-Risk Factors,
pubmed-meshheading:12500190-Tumor Necrosis Factor-alpha
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pubmed:year |
2003
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pubmed:articleTitle |
Interleukin-1beta gene polymorphisms associated with hepatocellular carcinoma in hepatitis C virus infection.
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pubmed:affiliation |
Department of Gastroenterology, Graduate School of Medicine, University of Tokyo, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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