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

被引:68
|
作者
Thompson, Alexander J. [1 ]
Patel, Keyur [1 ]
Chuang, Wan-Long [2 ]
Lawitz, Eric J. [3 ]
Rodriguez-Torres, Maribel [4 ]
Rustgi, Vinod K. [5 ]
Flisiak, Robert [6 ]
Pianko, Stephen [7 ]
Diago, Moises [8 ]
Arora, Sanjeev [9 ]
Foster, Graham R. [10 ,11 ]
Torbenson, Michael [12 ]
Benhamou, Yves [13 ]
Nelson, David R. [14 ]
Sulkowski, Mark S. [12 ]
Zeuzem, Stefan [15 ]
Pulkstenis, Erik [16 ]
Subramanian, G. Mani [1 ,16 ]
McHutchison, John G.
机构
[1] Duke Univ, Med Ctr, Duke Clin Res Inst, Durham, NC 27715 USA
[2] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Kaohsiung, Taiwan
[3] Alamo Med Res, San Antonio, TX USA
[4] Fdn Invest Diego, Santurce, PR USA
[5] Metropolitan Res, Fairfax, VA USA
[6] Med Univ Bialystok, Bialystok, Poland
[7] Monash Med Ctr, Clayton, Vic 3168, Australia
[8] Hosp Quiron Valencia, Barcelona, Spain
[9] Univ New Mexico, Albuquerque, NM 87131 USA
[10] Queen Mary Univ London, London, England
[11] Barts & London NHS Trust, London, England
[12] Johns Hopkins Ctr Viral Hepatitis, Baltimore, MD USA
[13] Hop La Pitie Salpetriere, Paris, France
[14] Univ Florida, Gainesville, FL USA
[15] JW Goethe Univ Hosp, Frankfurt, Germany
[16] Human Genome Sci Inc, Rockville, MD USA
基金
英国医学研究理事会;
关键词
SUSTAINED VIROLOGICAL RESPONSE; TYPE-2; DIABETES-MELLITUS; VIRUS-INFECTION; HEPATOCELLULAR-CARCINOMA; GLUCOSE ABNORMALITIES; RECEPTOR SUBSTRATE-1; COMBINATION THERAPY; FIBROSIS; PROTEIN; SENSITIVITY;
D O I
10.1136/gut.2010.236158
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 (delta 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, gamma-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.
引用
收藏
页码:128 / 134
页数:7
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