Division of Pediatric Gastroenterology and Nutrition, Johns Hopkins School of Medicine, Baltimore, MD, USA.
Am J Clin Nutr. 2012 Apr;95(4):892-900. doi: 10.3945/ajcn.111.020156. Epub 2012 Feb 15.
There is significant histologic and biochemical overlap between nonalcoholic fatty liver disease (NAFLD) and steatohepatitis associated with choline deficiency.
We sought to determine whether subjects with biopsy-proven NAFLD and evidence of an inadequate intake of choline had more severe histologic features.
We performed a cross-sectional analysis of 664 subjects enrolled in the multicenter, prospective Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN) with baseline data on diet composition (from a recall-based food-frequency questionnaire) within 6 mo of a liver biopsy. Food questionnaires were analyzed with proprietary software to estimate daily intakes of choline. Liver biopsies were centrally read, and consensus was scored with the NASH CRN-developed scoring system. Because choline needs vary by age, sex, and menopausal status, participants were segregated into corresponding categories (children 9-13 y old, males ≥14 y old, premenopausal women ≥19 y old, and postmenopausal women) on the basis of the Institute of Medicine's definition of adequate intake (AI) for choline. Deficient intake was defined as <50% AI.
Postmenopausal women with deficient choline intake had worse fibrosis (P = 0.002) once factors associated with NAFLD (age, race-ethnicity, obesity, elevated triglycerides, diabetes, alcohol use, and steroid use) were considered in multiple ordinal logistic regression models. Choline intake was not identified as a contributor to disease severity in children, men, or premenopausal women.
Decreased choline intake is significantly associated with increased fibrosis in postmenopausal women with NAFLD. The Pioglitazone vs Vitamin E vs Placebo for Treatment of Non-Diabetic Patients With Nonalcoholic Steatohepatitis trial was registered at clinicaltrials.gov as NCT00063622, and the Treatment of Nonalcoholic Fatty Liver Disease in Children trial was registered at clinicaltrials.gov as NCT00063635.
非酒精性脂肪性肝病(NAFLD)与胆碱缺乏相关的脂肪性肝炎在组织学和生物化学上有很大的重叠。
我们旨在确定活检证实为 NAFLD 且胆碱摄入不足的患者是否具有更严重的组织学特征。
我们对 664 例参加多中心、前瞻性非酒精性脂肪性肝炎临床研究网络(NASH CRN)的患者进行了横断面分析,这些患者在肝活检前 6 个月内进行了饮食成分的基线数据(来自基于回忆的食物频率问卷)。食物问卷通过专有软件进行分析,以估计胆碱的日摄入量。肝活检由中心读取,并使用 NASH CRN 开发的评分系统进行共识评分。由于胆碱的需求量因年龄、性别和绝经状态而异,因此根据医学研究所(IOM)对胆碱的充足摄入量(AI)的定义,将参与者分为相应的类别(9-13 岁的儿童、≥14 岁的男性、≥19 岁的绝经前女性和绝经后女性)。摄入不足定义为<50% AI。
在考虑了与 NAFLD 相关的因素(年龄、种族-民族、肥胖、甘油三酯升高、糖尿病、饮酒和类固醇使用)后,摄入胆碱不足的绝经后妇女的纤维化程度更差(P=0.002),在多个有序逻辑回归模型中。在儿童、男性或绝经前妇女中,胆碱摄入未被确定为疾病严重程度的一个因素。
在患有 NAFLD 的绝经后妇女中,胆碱摄入减少与纤维化增加显著相关。吡格列酮与维生素 E 或安慰剂治疗非糖尿病非酒精性脂肪性肝炎患者的试验在 clinicaltrials.gov 上注册为 NCT00063622,治疗儿童非酒精性脂肪性肝病的试验在 clinicaltrials.gov 上注册为 NCT00063635。