Helal Gouda K, Gad Magdy A, Abd-Ellah Mohamed F, Mahgoup Elsayed M
aDepartment of Pharmacology, Faculty of Pharmacy, Al-Azhar University, Cairo bDepartment of Hepatology, Gastroenterology and Infectious Diseases, Faculty of Medicine, Benha University, Benha, Egypt.
Eur J Gastroenterol Hepatol. 2016 May;28(5):553-7. doi: 10.1097/MEG.0000000000000587.
Ezetimibe has been reported to inhibit viral entry and to reduce BMI and has been proposed as a novel therapeutic agent for chronic hepatitis C (CHC), potentiating the effects of pegylated interferon and ribavirin (peg-IFN/RBV).
The aim of the study was to assess the effects of ezetimibe coadministration with peg-IFN/RBV combination on the early virological response (EVR) rates in nonobese and obese patients with CHC genotype 4 (CHC-4).
A total of 144 CHC-4 patients were divided into two groups; group 1 included nonobese patients (n=76) and group 2 included obese patients (n=68). Each group was further subclassified into equal control and treated groups. The control groups received peg-IFN/RBV combination for 24 weeks, and the treated groups received peg-IFN/RBV plus ezetimibe for 12 weeks and then only peg-IFN/RBV for the remaining 12 weeks.
The study revealed that EVR significantly improved in the obese patients (85.3 vs. 64.7% in the treated and control groups, respectively, at P<0.05) without any significant improvement in the nonobese patients. Biochemical responses (defined as normalization of alanine aminotransferase at week 12) were markedly improved in the treated groups in both the nonobese and obese groups compared with their respective controls.
The addition of ezetimibe to peg-IFN/RBV combination significantly improves EVR rates in obese patients compared with nonobese patients, and remarkably improves the biochemical responses in both obese and nonobese patients with CHC-4. This may shed light on a new strategy for the treatment of CHC, particularly in obese Egyptian patients.
依泽替米贝已被报道可抑制病毒进入并降低体重指数,并且已被提议作为一种新型治疗药物用于慢性丙型肝炎(CHC),增强聚乙二醇化干扰素和利巴韦林(聚乙二醇干扰素/利巴韦林,peg-IFN/RBV)的疗效。
本研究旨在评估依泽替米贝与聚乙二醇干扰素/利巴韦林联合用药对4型CHC(CHC-4)非肥胖和肥胖患者早期病毒学应答(EVR)率的影响。
总共144例CHC-4患者被分为两组;第1组包括非肥胖患者(n = 76),第2组包括肥胖患者(n = 68)。每组再进一步分为相等的对照组和治疗组。对照组接受聚乙二醇干扰素/利巴韦林联合用药24周,治疗组接受聚乙二醇干扰素/利巴韦林加依泽替米贝治疗12周,然后在剩余12周仅接受聚乙二醇干扰素/利巴韦林治疗。
研究显示,肥胖患者的EVR显著改善(治疗组和对照组分别为85.3%和64.7%,P<0.05),而非肥胖患者无显著改善。与各自的对照组相比,非肥胖和肥胖组的治疗组中生化应答(定义为第12周时丙氨酸转氨酶正常化)均显著改善。
与非肥胖患者相比,在聚乙二醇干扰素/利巴韦林联合用药中添加依泽替米贝可显著提高肥胖患者的EVR率,并显著改善CHC-4肥胖和非肥胖患者的生化应答。这可能为CHC的治疗,尤其是肥胖埃及患者的治疗,提供一种新策略。