Hoofnagle Jay H, Wahed Abdus S, Brown Robert S, Howell Charles D, Belle Steven H
Liver Disease Research Branch, Division of Digestive Diseases and Nutrition, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda 20817, USA.
J Infect Dis. 2009 Apr 15;199(8):1112-20. doi: 10.1086/597384.
Early changes in hepatitis C virus (HCV) RNA levels were assessed in a large cohort of African American and white patients with chronic hepatitis C due to HCV genotype 1 who underwent therapy with peginterferon alfa-2a and ribavirin in the Study of Viral Resistance to Antiviral Therapy of Hepatitis C (Virahep-C). Analyses were restricted to 341 patients who completed the first 28 days of therapy without dose modification. HCV RNA levels decreased in virtually all patients, but the amount of the change varied markedly. The overall 28-day decrease in HCV RNA levels was at least as predictive of a sustained virological response as the first- or second-phase viral kinetics responses. Factors associated with a smaller decrease in the HCV RNA level between baseline and day 28 included African American race, higher initial HCV RNA level, more severe hepatic fibrosis, and higher body weight. African American patients with similar 28-day decreases in viral levels as white patients were still less likely to achieve a sustained virological response. These results suggest that racial differences in the response to antiviral therapy are due to greater unresponsiveness to intracellular actions of interferon in African American individuals and that standard doses of peginterferon and ribavirin may be suboptimal for patients with higher body weights. Trial registration. ClinicalTrials.gov identifier: NCT00038974 .
在丙型肝炎抗病毒治疗病毒抗性研究(Virahep-C)中,对一大群因丙型肝炎病毒1型感染导致慢性丙型肝炎的非裔美国人和白人患者,评估了丙型肝炎病毒(HCV)RNA水平的早期变化。这些患者接受了聚乙二醇化干扰素α-2a和利巴韦林治疗。分析仅限于341例在未调整剂量的情况下完成治疗前28天的患者。几乎所有患者的HCV RNA水平均下降,但下降幅度差异显著。HCV RNA水平在28天内的总体下降情况与第一阶段或第二阶段病毒动力学反应一样,至少能预测持续病毒学应答。与基线至第28天HCV RNA水平下降较小相关的因素包括非裔美国人种族、初始HCV RNA水平较高、肝纤维化更严重以及体重较高。病毒水平在28天内下降情况与白人患者相似的非裔美国患者,实现持续病毒学应答的可能性仍然较低。这些结果表明,抗病毒治疗反应中的种族差异是由于非裔美国人个体对干扰素细胞内作用的反应性较低,并且对于体重较高的患者,标准剂量的聚乙二醇化干扰素和利巴韦林可能并非最佳选择。试验注册。ClinicalTrials.gov标识符:NCT00038974 。