Excess body weight, liver steatosis, and early fibrosis progression due to hepatitis C recurrence after liver transplantation

World J Gastroenterol. 2005 Oct 14;11(38):5944-50. doi: 10.3748/wjg.v11.i38.5944.

Abstract

Aim: To investigate how weight gain after OLT affects the speed of fibrosis progression (SFP) during recurrent hepatitis C virus (HCV) infection of the graft.

Methods: Ninety consecutive patients (63 males, median age 53 years; 55 with HCV-related liver disease), transplanted at a single institution, were studied. All were followed for at least 2 years after OLT and had at least one follow-up graft biopsy, performed not earlier than 1 year after the transplant operation. For each biopsy, a single, experienced pathologist gave an estimate of both the staging according to Ishak and the degree of hepatic steatosis. The SFP was quantified in fibrosis units/month (FU/mo). The lipid metabolism status of patients was summarized by the plasma triglycerides/cholesterol (T/C) ratio. Body mass index (BMI) was measured before OLT, and 1 and 2 years after it.

Results: In the HCV positive group, the highest SFP was observed in the first post-OLT year. At that time point, a SFP <=0.100 FU/mo was observed more frequently among recipients who had received their graft from a young donor and had a pre-transplant BMI value >26.0 kg/m(2). At completion of the first post-transplant year, a BMI value >26.5 kg/m(2) was associated with a T/C ratio <=1. The proportion of patients with SFP >0.100 FU/mo descended in the following order: female recipients with a high T/C ratio, male recipients with high T/C ratio, and recipients of either gender with low T/C ratio. Hepatic steatosis was observed more frequently in recipients who, in the first post-transplant year, had increased their BMI >=1.5 kg/m(2) in comparison to the pre-transplant value. Hepatic steatosis was inversely associated with the staging score.

Conclusion: Among HCV positive recipients, excess weight gain post-OLT does not represent a factor favoring early liver fibrosis development and might even be protective against it.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Fatty Liver / etiology
  • Female
  • Hepatitis C / etiology*
  • Hepatitis C / pathology
  • Hepatitis C / surgery
  • Humans
  • Lipids / blood
  • Liver Cirrhosis / etiology
  • Liver Transplantation / adverse effects*
  • Liver Transplantation / pathology
  • Longitudinal Studies
  • Male
  • Middle Aged
  • Recurrence
  • Retrospective Studies
  • Weight Gain

Substances

  • Lipids