Lack of association of some chemokine system polymorphisms with the risks of death and hepatocellular carcinoma occurrence in patients with alcoholic cirrhosis: a prospective study

Eur J Gastroenterol Hepatol. 2007 May;19(5):425-31. doi: 10.1097/MEG.0b013e3280120e2b.

Abstract

Background: Polymorphisms in genes encoding for the chemokines stromal cell-derived factor-1 (SDF-1)/CXCL12, monocyte chemotactic protein-1 (MCP-1)/CCL2, or for the chemokine receptors, CC chemokine receptor 5 (CCR5) or CC chemokine receptor 2 (CCR2) have been associated with the progression of hepatitis C virus-related liver injury and with various cancer development. Their influence on the prognosis of alcoholic liver disease is unknown.

Patients and methods: SDF-1 3'A, MCP-1(-2518), CCR5-Delta32 and CCR2-64I polymorphisms, SDF-1alpha, regulated upon activation normal T cells expressed and secreted (RANTES)/CCL5 and MCP-1 sera levels were determined in 222 alcoholic patients, included at the time of cirrhosis diagnosis and prospectively followed up.

Results: Carriers and noncarriers of each genetic marker had similar baseline characteristics estimating the severity of liver disease. Mean time of follow-up of the cohort was 62.9+/-43.2 months. One hundred and forty-seven out of 222 (66.3%) patients were alive at the end of the study. The occurrence of death (75/222; 33.7%) or hepatocellular carcinoma (67/222; 30.1%) during follow-up was similar among carriers and noncarriers of each polymorphism. No association between the carriage of mutated alleles and chemokine sera levels was found: CCR5-Delta32/RANTES, SDF-1 3'A/SDF-1alpha and CCR2-64I or MCP-1(-2518)/MCP-1. Baseline RANTES, SDF-1alpha and MCP-1 sera levels were associated neither with the risk of death nor with the risk of hepatocellular carcinoma.

Conclusions: The present study suggests the lack of association of SDF-1 3'A, MCP-1(-2518), CCR5-Delta32 and CCR2-64I polymorphisms with death and hepatocellular carcinoma occurrence in cirrhotic alcoholic patients.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Alcohol Drinking
  • Carcinoma, Hepatocellular / etiology
  • Carcinoma, Hepatocellular / genetics*
  • Chemokine CCL2 / blood
  • Chemokine CCL2 / genetics
  • Chemokine CCL5 / blood
  • Chemokine CXCL12
  • Chemokines / genetics*
  • Chemokines, CXC / blood
  • Chemokines, CXC / genetics
  • Epidemiologic Methods
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Liver Cirrhosis, Alcoholic / blood
  • Liver Cirrhosis, Alcoholic / complications
  • Liver Cirrhosis, Alcoholic / genetics*
  • Liver Neoplasms / etiology
  • Liver Neoplasms / genetics*
  • Male
  • Middle Aged
  • Polymorphism, Genetic*
  • Prognosis
  • Receptors, CCR2
  • Receptors, CCR5 / genetics
  • Receptors, Chemokine / genetics
  • Temperance

Substances

  • CCL2 protein, human
  • CCR2 protein, human
  • CXCL12 protein, human
  • Chemokine CCL2
  • Chemokine CCL5
  • Chemokine CXCL12
  • Chemokines
  • Chemokines, CXC
  • Receptors, CCR2
  • Receptors, CCR5
  • Receptors, Chemokine