Source:http://linkedlifedata.com/resource/pubmed/id/18940717
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2008-10-22
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pubmed:abstractText |
The production of transforming growth factor beta 1 (TGF-beta1) has been reported as being significantly associated with the gene polymorphism in the leader sequence at positions +29. The current study aimed to evaluate the associations between the polymorphism and the clinical characteristics of chronic hepatitis C (CHC). A total of 422 (252 men; mean age: 49.7 +/- 11.2 years) Taiwanese CHC patients with liver biopsies were enrolled. The TGF-beta1 gene polymorphism at position +29 (T or C), hepatitis C virus (HCV) RNA genotypes, and serum HCV RNA levels of these patients were determined. Of the 422 patients, the frequency of the T allele was 45.4%. Based on univariate analyses, a significantly lesser proportion of patients with allele T had high viral loads than those who were without allele T (P = 0.026). The lesser HCV RNA levels and HCV genotype 1b infection were significantly associated with the inheritance of the T allele in female patients based on univariate (P = 0.012 and 0.007, respectively) and multivariate regression (odds ratio/95% confidence interval: 0.434/0.219-0.859 and 0.468/0.237-0.927, respectively) analyses. In male patients with or without inheritance of the T allele, the clinical characteristics were similar. In conclusion, the association between TGF-beta1 polymorphism and virologic characteristics of chronic HCV infection implicated a significant role of host genetic factors on the clinical features of CHC. Female patients who carry T allele at position +29 were predisposed to be associated with HCV genotype non-1b infection and lesser HCV viral load, which revealed the gender effect.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1931-5244
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pubmed:author |
pubmed-author:ChangWen-YuWY,
pubmed-author:ChenShinn-CherngSC,
pubmed-author:ChuangWan-LongWL,
pubmed-author:DaiChia-YenCY,
pubmed-author:HouNai-JenNJ,
pubmed-author:HsiehMing-YenMY,
pubmed-author:HsiehMing-YuhMY,
pubmed-author:HuangJee-FuJF,
pubmed-author:LeeLi-PoLP,
pubmed-author:LinZu-YauZY,
pubmed-author:PanWen-ChengWC,
pubmed-author:WangLiang-YenLY,
pubmed-author:YuMing-LungML
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pubmed:issnType |
Print
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pubmed:volume |
152
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
151-6
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pubmed:meshHeading |
pubmed-meshheading:18940717-Alanine Transaminase,
pubmed-meshheading:18940717-Aspartate Aminotransferases,
pubmed-meshheading:18940717-Female,
pubmed-meshheading:18940717-Gene Frequency,
pubmed-meshheading:18940717-Genetic Predisposition to Disease,
pubmed-meshheading:18940717-Hepacivirus,
pubmed-meshheading:18940717-Hepatitis C, Chronic,
pubmed-meshheading:18940717-Humans,
pubmed-meshheading:18940717-Liver,
pubmed-meshheading:18940717-Logistic Models,
pubmed-meshheading:18940717-Male,
pubmed-meshheading:18940717-Middle Aged,
pubmed-meshheading:18940717-Polymorphism, Single Nucleotide,
pubmed-meshheading:18940717-RNA, Viral,
pubmed-meshheading:18940717-Taiwan,
pubmed-meshheading:18940717-Transforming Growth Factor beta1,
pubmed-meshheading:18940717-Viral Load
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pubmed:year |
2008
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pubmed:articleTitle |
Association between transforming growth factor-beta 1 polymorphism and virologic characteristics of chronic hepatitis C.
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pubmed:affiliation |
Hepatobiliary Division, Department of Internal Medicine, the Department of Occupational and Environmental Medicine, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Kaohsiung 807, Taiwan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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