Division of Gastroenterology, Department of Internal Medicine, Nippon Medical School Chiba Hokusoh Hospital, Chiba, Japan.
J Gastroenterol Hepatol. 2013 Jan;28(1):51-6. doi: 10.1111/j.1440-1746.2012.07267.x.
Although the anti-hepatitis C virus (HCV) effect of statins in vitro and clinical efficacy of fluvastatin combined with Pegylated interferon (PEG-IFN)/ribavirin therapy for chronic hepatitis C (CHC) have been reported, the details of clinical presentation are largely unknown. We focused on viral relapse that influences treatment outcome, and performed a post-hoc analysis by using data from a randomized controlled trial.
Thirty-four patients in the fluvastatin group and 33 patients in the non-fluvastatin group who achieved virological response (complete early virological response [cEVR] or late virological response [LVR]) with PEG-IFN/ribavirin therapy were subjected to this analysis. Factors contributing to viral relapse were identified by using multiple logistic regression analysis.
Relapse rate in patients with cEVR was significantly lower in the fluvastatin group (2 of 23, 8.7%) than in the non-fluvastatin group (9 of 26, 34.6%; P = 0.042). The use of fluvastatin decreased relapse rate in patients with LVR (27.3% vs 57.1%), though not significantly. Overall, relapse rate was significantly lower in the fluvastatin group (14.7%; 5 of 34) than in the non-fluvastatin group (39.4%; 13 of 33; P = 0.027). Multivariate analysis identified absence of fluvastatin (P = 0.027, odds ratio [OR] = 3.98, 95% confidence interval [CI] = 1.05-15.11) and low total ribavirin dose (P = 0.002, OR = 2.41, 95% CI = 1.38-4.19) as independent factors contributing to relapse.
The concomitant addition of fluvastatin significantly suppressed viral relapse, resulting in the improvement of sustained virological response rate, in PEG-IFN/ribavirin therapy for CHC patients with HCV genotype 1b and high viral load.
尽管已有研究表明他汀类药物具有体外抗丙型肝炎病毒(HCV)作用,以及氟伐他汀联合聚乙二醇干扰素(PEG-IFN)/利巴韦林治疗慢性丙型肝炎(CHC)的临床疗效,但对于具体的临床表现仍知之甚少。我们重点关注影响治疗效果的病毒复发,并利用一项随机对照试验的数据进行了事后分析。
对接受 PEG-IFN/利巴韦林治疗后获得病毒学应答(完全早期病毒学应答[cEVR]或晚期病毒学应答[LVR])的氟伐他汀组 34 例患者和非氟伐他汀组 33 例患者进行了此项分析。采用多因素逻辑回归分析确定病毒复发的相关因素。
cEVR 患者中氟伐他汀组的复发率明显低于非氟伐他汀组(23 例中有 2 例,8.7% vs 26 例中有 9 例,34.6%;P = 0.042)。氟伐他汀的使用降低了 LVR 患者的复发率(27.3% vs 57.1%),但差异无统计学意义。总体而言,氟伐他汀组的复发率明显低于非氟伐他汀组(14.7%,5 例;33 例中有 13 例,39.4%;P = 0.027)。多因素分析确定未使用氟伐他汀(P = 0.027,比值比[OR] = 3.98,95%置信区间[CI] = 1.05-15.11)和低总利巴韦林剂量(P = 0.002,OR = 2.41,95% CI = 1.38-4.19)是导致复发的独立因素。
氟伐他汀的联合应用可显著抑制病毒复发,从而提高 HCV 基因型 1b 且病毒载量高的 CHC 患者接受 PEG-IFN/利巴韦林治疗的持续病毒学应答率。