Diago M, Castellano G, García-Samaniego J, Pérez C, Fernández I, Romero M, Iacono O L, García-Monzón C
Section of Hepatology, University General Hospital, Valencia, Spain.
Gut. 2006 Mar;55(3):374-9. doi: 10.1136/gut.2005.074062. Epub 2005 Sep 8.
Increased serum and intrahepatic interferon gamma inducible protein 10 (IP-10) levels in patients with chronic hepatitis C (CHC) have been described.
To analyse the possible association of serum IP-10 levels with different outcomes to antiviral therapy.
A total of 137 CHC patients treated with peginterferon plus ribavirin.
Serum IP-10 levels were determined by enzyme linked immunosorbent assay before therapy, after 12 weeks of treatment, and 24 weeks after cessation of therapy. Variables significantly associated with a sustained virological response (SVR) on univariate analysis were included in a multivariate logistic regression model.
Pretreatment serum IP-10 levels in patients with SVR were significantly lower than in non-responders (NR) (332.4 (222.1) v 476.8 (305.3) pg/ml, respectively; p=0.004). Serum IP-10 concentrations significantly decreased in patients with SVR (pretreatment: 332.4 (222.1) pg/ml; post-treatment: 170.2 (140.1) pg/ml; p<0.001) but not in NR (pretreatment: 476.8 (305.3) pg/ml; post treatment: 387.3 (268.1) pg/ml; p=0.06). By multivariate analysis, non-1 genotype (odds ratio (OR) 3.5 (95% confidence interval (CI) 1.1-10.4); p=0.003) and low viral load at baseline (OR 0.34 (95% CI 0.14-0.79); p=0.01) were independent predictors of SVR in all patients. When multivariate analysis was restricted to patients with genotype 1, only baseline viral load (OR 0.38 (95% CI 0.155-0.96); p=0.04) and pretreatment serum IP-10 levels (OR 0.99 (95% CI 0.996-0.999); p=0.03) were identified as predictive factors of SVR.
Pretreatment serum IP-10 behaves as a predictive factor of SVR to peginterferon plus ribavirin therapy in genotype 1 infected patients.
已有报道称慢性丙型肝炎(CHC)患者血清及肝内干扰素γ诱导蛋白10(IP-10)水平升高。
分析血清IP-10水平与抗病毒治疗不同结局之间的可能关联。
共137例接受聚乙二醇干扰素联合利巴韦林治疗的CHC患者。
采用酶联免疫吸附测定法在治疗前、治疗12周后及治疗停止后24周测定血清IP-10水平。单因素分析中与持续病毒学应答(SVR)显著相关的变量纳入多因素逻辑回归模型。
SVR患者治疗前血清IP-10水平显著低于无应答者(NR)(分别为332.4(222.1)与476.8(305.3)pg/ml;p = 0.004)。SVR患者血清IP-10浓度显著降低(治疗前:332.4(222.1)pg/ml;治疗后:170.2(140.1)pg/ml;p < 0.001),但NR患者未降低(治疗前:476.8(305.3)pg/ml;治疗后:387.3(268.1)pg/ml;p = 0.06)。多因素分析显示,非1基因型(比值比(OR)3.5(95%置信区间(CI)1.1 - 10.4);p = 0.003)和基线低病毒载量(OR 0.34(95% CI 0.14 - 0.79);p = 0.01)是所有患者SVR的独立预测因素。当多因素分析仅限于1基因型患者时,仅基线病毒载量(OR 0.38(95% CI 0.155 - 0.96);p = 0.04)和治疗前血清IP-10水平(OR 0.99(95% CI 0.996 - 0.999);p = 0.03)被确定为SVR的预测因素。
治疗前血清IP-10是1基因型感染患者对聚乙二醇干扰素联合利巴韦林治疗SVR的预测因素。