Pellicano Rinaldo, Puglisi Giovanni, Ciancio Alessia, Balzola Federico, Saracco Giorgio, Ciccone Giovannino, Baldi Ileana, Abate Maria Lorena, Smedile Antonina, Rizzetto Mario
Department of Gastro-Hepatology, San Giovanni Battista (Molinette) Hospital, Torino, Italy.
J Med Virol. 2008 Apr;80(4):628-31. doi: 10.1002/jmv.21123.
Several factors, including metabolic profile, are predictive of response to standard antiviral therapy in patients with chronic hepatitis C. In a retrospective study, it was investigated whether uric acid, involved in metabolic syndrome, could be included. A total of 153 patients (56.2% males; mean age 45.7 +/- 11.3 years) treated with pegylated-interferon and ribavirin were included. Eighty-five were infected with hepatitis C virus (HCV) genotype 1 or 4 and 68 with genotype 2 or 3. Viral load was >1,000,000 IU/ml in 101, < or =1,000,000 IU/ml in 35 and unknown in 17 patients. Ishak fibrosis score was < or =4 in 81, >4 in 15 and unknown in 57 patients. Mean serum uric acid was 5.05 +/- 1.3 mg/dl. Sustained virological response (negative serum HCV-RNA 6 months after treatment cessation) was achieved in 102 patients (67%). In the final logistic model, serum uric acid level > or =5.8 mg/dl (OR = 0.46; 95% CI: 0.30-0.62), viral load (OR = 0.29; 95% CI: 0.09-0.92) and HCV genotype (OR = 0.23; 95% CI: 0.09-0.60) were identified as the most important factors independently influencing clinical outcome. The prognostic role of serum uric acid was confirmed on the sub-sample reporting Ishak fibrosis score (OR = 0.49; 95% CI: 0.28-0.85). Serum uric acid level > or =5.8 mg/dl is predictive of poor response to HCV treatment. Prospective studies are needed to clarify the issue.
包括代谢谱在内的多种因素可预测慢性丙型肝炎患者对标准抗病毒治疗的反应。在一项回顾性研究中,对参与代谢综合征的尿酸是否可纳入其中进行了调查。共有153例接受聚乙二醇干扰素和利巴韦林治疗的患者(男性占56.2%;平均年龄45.7±11.3岁)纳入研究。其中85例感染丙型肝炎病毒(HCV)基因1型或4型,68例感染基因2型或3型。101例患者病毒载量>1,000,000 IU/ml,35例≤1,000,000 IU/ml,17例患者病毒载量未知。81例患者Ishak纤维化评分≤4,15例>4,57例未知。血清尿酸平均水平为5.05±1.3 mg/dl。102例患者(67%)实现了持续病毒学应答(治疗停止6个月后血清HCV-RNA阴性)。在最终的逻辑模型中,血清尿酸水平≥5.8 mg/dl(比值比[OR]=0.46;95%可信区间[CI]:0.30-0.62)、病毒载量(OR=0.29;95% CI:0.09-0.92)和HCV基因型(OR=0.23;95% CI:0.09-0.60)被确定为独立影响临床结局的最重要因素。血清尿酸的预后作用在报告Ishak纤维化评分的子样本中得到证实(OR=0.49;95% CI:0.28-0.85)。血清尿酸水平≥5.8 mg/dl可预测HCV治疗反应不佳。需要进行前瞻性研究以阐明该问题。