Abstract
Background The hepatitis C virus (HCV) is known to disrupt lipid metabolism, making serum lipoprotein levels good candidates to explore as markers of HCV disease progression. Assessment of the major apolipoproteins (Apo) and their relationship to hepatic fibrosis remain largely unexplored.
Methods We compared the levels of total cholesterol, triglycerides, low-density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C), and Apo A-I, -B, -C-III, and -E between patients with cleared versus active infection (n = 83), and between those chronically infected patients (n = 216) with advanced versus mild-moderate hepatic fibrosis (METAVIR stage F3-4 vs. F0-2) using multiple logistic regression.
Results Apo C-III levels were 25% higher in subjects with cleared infection versus those with active infection (p = 0.009). Low levels of Apo C-III (p = 1.3 × 10 -5), Apo A-I (p = 2.9 × 10 -5), total cholesterol (p = 5.0 × 10 -4), LDL-C (p = 0.005), and HDL-C (p = 2.0 × 10 -4) were associated with advanced fibrosis in univariate analyses. Multivariable analysis revealed Apo C-III as the most significant factor associated with advanced fibrosis (p = 0.0004), followed by age (p = 0.013) and Apo A-I (p = 0.022). Inclusion of both Apo C-III and Apo A-I in a model to predict advanced fibrosis improved the area under the receiver operator curve only modestly.
Conclusions Relative to other lipoproteins, low serum Apo C-III levels are the most strongly associated with chronic versus cleared infection and decline with increasing severity of hepatic fibrosis. Apo C-III deserves further attention as a possible marker of HCV disease progression. © Asian Pacific Association for the Study of the Liver 2011.
| Original language | English |
|---|---|
| Pages (from-to) | 475-481 |
| Journal | Hepatology International |
| Volume | 6 |
| Issue number | 2 |
| Online published | 7 Jul 2011 |
| DOIs | |
| Publication status | Published - Apr 2012 |
| Externally published | Yes |
Funding
This study was funded in large part by a generous grant from the David H Murdock Institute for Business and Culture via the M.U.R.D.O.C.K. Study and NIH CTSA award 1 UL1 RR024128-01. Dr. Rowell is supported by NIH Training Grant T32-DK007012-31 at Duke University Medical Center. Dr. Thompson received funding support from the Duke Clinical Research Institute, a generous research gift from the Richard B. Boebel Family Fund, the National Health and Medical Research Council of Australia, and the Gastroenterology Society of Australia.
Research Keywords
- Apolipoprotein AI
- Apolipoprotein C-III
- Fibrosis
- Hepatitis C virus