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pubmed-article:10843744pubmed:abstractTextIn the liver, transforming growth factor (TGF) -beta(1)is primarily responsible for activation of fat-storing cells, which are the main source of extracellular matrix proteins. Their deposition play a key role in the development of liver cirrhosis. The aim of this study was to evaluate plasma TGF-beta(1)in patients with different stages of liver cirrhosis and its possible use as an indicator of liver function impairment. TGF-beta(1)was measured in the plasma of 40 patients with liver cirrhosis. To estimate possible effect of liver insufficiency on plasma TGF-beta(1), patients were divided into three groups: A, B and C, univocal with Child-Pugh classes. Normal values were collected from 13 healthy volunteers. Liver cirrhosis resulted in a significant increase of plasma concentration of TGF-beta(1)(39.3+/-3.8 ng/ml), which doubled normal values (18.3+/-1.6 ng/ml). The highest concentrations were observed in alcoholic patients (44.4+/-4.7 ng/ml). TGF-beta(1)level increased depending on the degree of liver insufficiency, demonstrated by a significant positive correlation with Child-Pugh score (r=0.591). Values in group A were similar to normal, but were significantly elevated in groups B and C. These findings suggest possible use of plasma TGF-beta(1)measurement as an indicator of liver function impairment and possible marker of hepatic fibrosis progression in cirrhotic patients.lld:pubmed
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pubmed-article:10843744pubmed:copyrightInfoCopyright 2000 Academic Press.lld:pubmed
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pubmed-article:10843744pubmed:pagination677-81lld:pubmed
pubmed-article:10843744pubmed:dateRevised2004-11-17lld:pubmed
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pubmed-article:10843744pubmed:articleTitleCirculating transforming growth factor beta(1) as an indicator of hepatic function impairment in liver cirrhosis.lld:pubmed
pubmed-article:10843744pubmed:affiliationDepartment of Infectious Diseases, Medical Academy of Bialystok, Bialystok, Poland. flisiakr@priv.onet.pllld:pubmed
pubmed-article:10843744pubmed:publicationTypeJournal Articlelld:pubmed
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