Lavine Joel E, Schwimmer Jeffrey B, Van Natta Mark L, Molleston Jean P, Murray Karen F, Rosenthal Philip, Abrams Stephanie H, Scheimann Ann O, Sanyal Arun J, Chalasani Naga, Tonascia James, Ünalp Aynur, Clark Jeanne M, Brunt Elizabeth M, Kleiner David E, Hoofnagle Jay H, Robuck Patricia R
Department of Pediatrics, Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Columbia University, New York, New York, USA.
JAMA. 2011 Apr 27;305(16):1659-68. doi: 10.1001/jama.2011.520.
Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disease in US children and adolescents and can present with advanced fibrosis or nonalcoholic steatohepatitis (NASH). No treatment has been established.
To determine whether children with NAFLD would improve from therapeutic intervention with vitamin E or metformin.
DESIGN, SETTING, AND PATIENTS: Randomized, double-blind, double-dummy, placebo-controlled clinical trial conducted at 10 university clinical research centers in 173 patients (aged 8-17 years) with biopsy-confirmed NAFLD conducted between September 2005 and March 2010. Interventions Daily dosing of 800 IU of vitamin E (58 patients), 1000 mg of metformin (57 patients), or placebo (58 patients) for 96 weeks.
The primary outcome was sustained reduction in alanine aminotransferase (ALT) defined as 50% or less of the baseline level or 40 U/L or less at visits every 12 weeks from 48 to 96 weeks of treatment. Improvements in histological features of NAFLD and resolution of NASH were secondary outcome measures.
Sustained reduction in ALT level was similar to placebo (10/58; 17%; 95% CI, 9% to 29%) in both the vitamin E (15/58; 26%; 95% CI, 15% to 39%; P = .26) and metformin treatment groups (9/57; 16%; 95% CI, 7% to 28%; P = .83). The mean change in ALT level from baseline to 96 weeks was -35.2 U/L (95% CI, -56.9 to -13.5) with placebo vs -48.3 U/L (95% CI, -66.8 to -29.8) with vitamin E (P = .07) and -41.7 U/L (95% CI, -62.9 to -20.5) with metformin (P = .40). The mean change at 96 weeks in hepatocellular ballooning scores was 0.1 with placebo (95% CI, -0.2 to 0.3) vs -0.5 with vitamin E (95% CI, -0.8 to -0.3; P = .006) and -0.3 with metformin (95% CI, -0.6 to -0.0; P = .04); and in NAFLD activity score, -0.7 with placebo (95% CI, -1.3 to -0.2) vs -1.8 with vitamin E (95% CI, -2.4 to -1.2; P = .02) and -1.1 with metformin (95% CI, -1.7 to -0.5; P = .25). Among children with NASH, the proportion who resolved at 96 weeks was 28% with placebo (95% CI, 15% to 45%; 11/39) vs 58% with vitamin E (95% CI, 42% to 73%; 25/43; P = .006) and 41% with metformin (95% CI, 26% to 58%; 16/39; P = .23). Compared with placebo, neither therapy demonstrated significant improvements in other histological features.
Neither vitamin E nor metformin was superior to placebo in attaining the primary outcome of sustained reduction in ALT level in patients with pediatric NAFLD.
clinicaltrials.gov Identifier: NCT00063635.
非酒精性脂肪性肝病(NAFLD)是美国儿童和青少年中最常见的慢性肝病,可出现晚期纤维化或非酒精性脂肪性肝炎(NASH)。目前尚未确立治疗方法。
确定NAFLD患儿接受维生素E或二甲双胍治疗干预后是否会有所改善。
设计、地点和患者:在10个大学临床研究中心进行的随机、双盲、双模拟、安慰剂对照临床试验,纳入173例(8至17岁)经活检确诊为NAFLD的患者,研究时间为2005年9月至2010年3月。干预措施为每日服用800 IU维生素E(58例患者)、1000 mg二甲双胍(57例患者)或安慰剂(58例患者),为期96周。
主要结局为丙氨酸氨基转移酶(ALT)持续降低,定义为治疗48至96周期间每12周访视时ALT水平降至基线水平的50%或更低或40 U/L或更低。NAFLD组织学特征的改善和NASH的缓解为次要观察指标。
维生素E治疗组(15/58;26%;95%CI,15%至39%;P = 0.26)和二甲双胍治疗组(9/57;16%;95%CI,7%至28%;P = 0.83)中ALT水平持续降低的情况与安慰剂组(10/58;17%;95%CI,9%至29%)相似。从基线到96周,安慰剂组ALT水平的平均变化为-35.2 U/L(95%CI,-56.9至-13.5),维生素E组为-48.3 U/L(95%CI,-66.8至-29.8)(P = 0.07),二甲双胍组为-41.7 U/L(95%CI,-62.9至-20.5)(P = 0.40)。96周时肝细胞气球样变评分的平均变化,安慰剂组为0.1(95%CI,-0.2至0.3),维生素E组为-0.5(95%CI,-0.8至-0.3;P = 0.006),二甲双胍组为-0.3(95%CI,-0.6至-0.0;P = 0.04);NAFLD活动评分方面,安慰剂组为-0.7(95%CI,-1.3至-0.2),维生素E组为-1.8(95%CI,-2.4至-1.2;P = 0.02),二甲双胍组为-?1.1(95%CI,-1.7至-0.5;P = 0.25)。在患有NASH的儿童中,96周时病情缓解的比例安慰剂组为28%(95%CI,15%至45%;11/39),维生素E组为58%(95%CI,42%至73%;25/43;P = 0.006),二甲双胍组为41%(95%CI,26%至58%;16/39;P = 0.23)。与安慰剂相比,两种治疗方法在其他组织学特征方面均未显示出显著改善。
在实现小儿NAFLD患者ALT水平持续降低这一主要结局方面,维生素E和二甲双胍均不优于安慰剂。
clinicaltrials.gov标识符:NCT00063635 。