Abstract | AIM: METHODS: SDF-1 3'A, MCP-1 (-2518) and CCR5-Delta32 polymorphisms, SDF-1 alpha, Regulated upon Activation Normal T cells Expressed and Secreted ( RANTES)/CCL5 and MCP-1 serum levels were determined in 120 HCV-infected patients, included at time of cirrhosis diagnosis and prospectively followed-up. RESULTS: During follow-up, 23/120 (19.1%) patients died and 47/120 (39.1%) developed HCC. Carriers and noncarriers of each genetic marker had similar baseline characteristics estimating the severity of liver disease. The occurrence of death or HCC during follow-up was similar among carriers and noncarriers of each polymorphism. There was no association between the carriage of mutated alleles and chemokine serum levels and the latter were not associated with the risks of death or HCC. CONCLUSION: This study suggests the lack of association of SDF-1 3'A, MCP-1 (-2518), CCR5-Delta32 polymorphisms with death and HCC occurrence in cirrhotic HCV-infected patients.
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Authors | Pierre Nahon, Angela Sutton, Pierre Rufat, Chantal Simon, Jean-Claude Trinchet, Liliane Gattegno, Michel Beaugrand, Nathalie Charnaux |
Journal | World journal of gastroenterology
(World J Gastroenterol)
Vol. 14
Issue 5
Pg. 713-9
(Feb 07 2008)
ISSN: 1007-9327 [Print] United States |
PMID | 18205260
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- CCL2 protein, human
- CXCL12 protein, human
- Chemokine CCL2
- Chemokine CXCL12
- Receptors, CCR5
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Topics |
- Aged
- Carcinoma, Hepatocellular
(genetics, mortality, virology)
- Chemokine CCL2
(genetics)
- Chemokine CXCL12
(genetics)
- Female
- Hepatitis C, Chronic
(genetics, immunology, mortality)
- Humans
- Incidence
- Liver Cirrhosis
(genetics, immunology, mortality)
- Liver Neoplasms
(genetics, mortality, virology)
- Male
- Middle Aged
- Polymorphism, Genetic
- Receptors, CCR5
(genetics)
- Survival Analysis
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