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Viral clearance is associated with improved insulin resistance in genotype 1 chronic hepatitis C but not genotype 2/3.

Authors :
Thompson, Alexander J.
Patel, Keyur
Wan-Long Chuang
Lawitz, Eric J.
Rodriguez-Torres, Maribel
Rustgi, Vinod K.
Flisiak, Robert
Pianko, Stephen
Diago, Moises
Arora, Sanjeev
Foster, Graham R.
Torbenson, Michael
Benhamou, Yves
Nelson, David R.
Sulkowski, Mark S.
Zeuzem, Stefan
Pulkstenis, Erik
Subramanian, G. Mani
McHutchison, John G.
Source :
Gut. Jan2012, Vol. 61 Issue 1, p128-134. 7p. 4 Charts, 2 Graphs.
Publication Year :
2012

Abstract

Objectives Genotype-specific associations between hepatitis C virus (HCV) and insulin resistance (IR) have been described, but a causal relationship remains unclear. This study investigated the association between a sustained virological response (SVR) and IR after chronic HCV therapy. Methods 2255 treatment-naive patients with chronic HCV genotype 1 or 2/3 were enrolled in two phase 3 trials of albinterferon alpha-2b versus pegylated interferon alpha-2a for 48 or 24 weeks, respectively. IR was measured before treatment and 12 weeks after treatment using homeostasis model assessment (HOMA)-IR. Results Paired HOMA-IR measurements were available in 1038 non-diabetic patients (497 with genotype 1; 541 with genotype 2/3). At baseline the prevalence of HOMA-IR >3 was greater in patients with genotype 1 than 2/3 (33% vs 27%; p=0.048). There was a significant reduction in the prevalence of IR in patients with genotype 1 achieving SVR (δ 10%; p<0.001), but not in genotype 1 non-responders or those with genotype 2/3. Multivariate analysis indicated that SVR was associated with a significant reduction in mean HOMA-IR in patients with genotype 1 (p=0.004), but not in those with genotype 2/3, which was independent of body mass index, alanine transaminase, γ-glutamyl transpeptidase and lipid level changes. Conclusions SVR is associated with a reduction in HOMA-IR in patients with HCV genotype 1 but not in those with genotype 2/3. Genotype 1 may have a direct effect on the development of IR, independent of host metabolic factors, and may be partially reversed by viral eradication. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00175749
Volume :
61
Issue :
1
Database :
Academic Search Index
Journal :
Gut
Publication Type :
Academic Journal
Accession number :
69694293
Full Text :
https://doi.org/10.1136/gut.2010.236158