Department of Gastroenterology and Hepatology, Saiseikai Suita Hospital, 1-2 Kawazono-cho, Suita, Osaka, 564-0013, Japan.
J Gastroenterol. 2011 Jan;46(1):101-7. doi: 10.1007/s00535-010-0291-8. Epub 2010 Jul 24.
Hyperlipidemia, insulin resistance, and oxidative stress can heavily contribute to the initiation and progression of nonalcoholic fatty liver disease (NAFLD). Currently, there is no established treatment for this disease. Recently, several studies have shown that ezetimibe (EZ), a lipid-lowering drug, attenuates liver steatosis in an experimental NAFLD model. This study was designed to assess the efficacy of long-term EZ monotherapy in patients with NAFLD.
A total of 45 patients with newly diagnosed liver biopsy-proven NAFLD were treated with EZ (10 mg/day) for 24 months. NAFLD-related biochemical parameters, imaging by computerized tomography, and liver biopsy were studied before and after treatment.
Ezetimibe therapy significantly improved NAFLD-related metabolic parameters including visceral fat area, fasting insulin, homeostasis model assessment of insulin resistance (HOMA-R), triglycerides, total cholesterol, low-density lipoprotein cholesterol (LDL-Ch), oxidative-LDL, the net electronegative charge modified-LDL, profiles of lipoprotein particle size and fatty acids component, and estimated desaturase activity. EZ therapy also significantly lowered serum alanine aminotransferase and high-sensitivity C-reactive protein levels, whereas no significant changes were found in serum type IV collagen 7S, adiponectin, leptin, and resistin levels. Histological features of steatosis grade (P = 0.0003), necroinflammatory grade (P = 0.0456), ballooning score (P = 0.0253), and NAFLD activity score (NAS) (P = 0.0007) were significantly improved from baseline. However, the fibrosis stage was not significantly (P = 0.6547) changed.
The results in this study suggest that the long-term EZ therapy can lead to improvement in metabolic, biochemical, and histological abnormalities of NAFLD. Therefore, EZ may be a promising agent for treatment of NAFLD.
高脂血症、胰岛素抵抗和氧化应激可大大促进非酒精性脂肪性肝病(NAFLD)的发生和发展。目前,尚无针对该病的既定治疗方法。最近,多项研究表明,降脂药依泽替米贝(EZ)可减轻实验性 NAFLD 模型中的肝脂肪变性。本研究旨在评估 EZ 单药长期治疗 NAFLD 患者的疗效。
共 45 例经肝活检证实的初诊 NAFLD 患者接受 EZ(10 mg/天)治疗 24 个月。在治疗前后研究了与 NAFLD 相关的生化参数、计算机断层扫描成像和肝活检。
EZ 治疗可显著改善与 NAFLD 相关的代谢参数,包括内脏脂肪面积、空腹胰岛素、胰岛素抵抗评估的稳态模型(HOMA-R)、甘油三酯、总胆固醇、低密度脂蛋白胆固醇(LDL-Ch)、氧化型 LDL、经净负电荷修饰的 LDL、脂蛋白颗粒大小和脂肪酸成分谱以及估计的去饱和酶活性。EZ 治疗还显著降低了血清丙氨酸氨基转移酶和高敏 C 反应蛋白水平,而血清 IV 型胶原 7S、脂联素、瘦素和抵抗素水平无明显变化。肝组织学脂肪变性程度评分(P = 0.0003)、坏死性炎症程度评分(P = 0.0456)、气球样变评分(P = 0.0253)和 NAFLD 活动评分(NAS)(P = 0.0007)均较基线显著改善。然而,纤维化分期无显著变化(P = 0.6547)。
本研究结果表明,EZ 长期治疗可改善 NAFLD 的代谢、生化和组织学异常。因此,EZ 可能是治疗 NAFLD 的一种有前途的药物。