Laboratory for Digestive Diseases, Center for Genomic Medicine, RIKEN, Hiroshima, Japan.
J Viral Hepat. 2012 Feb;19(2):e126-33. doi: 10.1111/j.1365-2893.2011.01516.x. Epub 2011 Sep 14.
Obesity and insulin resistance have been reported as negative predictors for sustained virological response (SVR) in hepatitis C virus (HCV) genotype 1 infected patients treated with pegylated interferon-α plus ribavirin. They are also known to affect serum levels of several cytokines including adipocytokines. But the association between these cytokines and treatment outcome has not been fully elucidated. We examined pretreatment serum levels of 14 cytokines among 190 patients who were treated with pegylated interferon-α-2b plus ribavirin for chronic HCV-1b infection with high viral load (≥ 5 log IU/mL) and analyzed their contribution to treatment response. Plasminogen activator inhibitor-1 (PAI-1), vascular endothelial growth factor, and 11 clinical factors showed significant association with SVR in univariate logistic regression analysis. Four significant factors in multivariate analysis; serum PAI-1 (odds ratio [OR] = 15.42), body mass index (OR = 4.56), rs8099917 (OR = 4.95) and fibrosis stage (OR = 5.18) were identified as independent predictors. We constructed a simple and minimally invasive prediction score for SVR based on the presence of these factors except for fibrosis stage. The accuracy of this score was 73%, and was confirmed using an independent validation cohort consisting of 31 patients (68%). The strongest correlation was between PAI-1 level and platelet count (r = 0.38, P = 1.8 × 10(-7)), and PAI-1 level was inversely correlated with fibrosis stage. Serum PAI-1 is a novel predictor for the response to combination therapy against chronic HCV-1b infection and may be associated with liver fibrosis.
肥胖和胰岛素抵抗已被报道为丙型肝炎病毒(HCV)基因型 1 感染患者接受聚乙二醇干扰素-α加利巴韦林治疗后持续病毒学应答(SVR)的负面预测因子。它们也已知会影响几种细胞因子的血清水平,包括脂肪细胞因子。但是这些细胞因子与治疗结果之间的关系尚未完全阐明。我们在 190 例慢性 HCV-1b 感染高病毒载量(≥5 log IU/mL)患者中检查了聚乙二醇干扰素-α-2b 加利巴韦林治疗前的 14 种细胞因子的血清水平,并分析了它们对治疗反应的贡献。纤溶酶原激活物抑制剂-1(PAI-1)、血管内皮生长因子和 11 个临床因素在单变量逻辑回归分析中与 SVR 有显著相关性。多变量分析中的四个显著因素;血清 PAI-1(优势比[OR] = 15.42)、体重指数(OR = 4.56)、rs8099917(OR = 4.95)和纤维化分期(OR = 5.18)被确定为独立预测因子。我们构建了一个基于这些因素(除了纤维化分期)存在的简单且微创的 SVR 预测评分。该评分的准确性为 73%,并通过包含 31 例患者的独立验证队列得到了证实(68%)。PAI-1 水平与血小板计数之间的相关性最强(r = 0.38,P = 1.8×10(-7)),且 PAI-1 水平与纤维化分期呈负相关。血清 PAI-1 是丙型肝炎病毒 1b 慢性感染联合治疗反应的新预测因子,可能与肝纤维化有关。