Chen Vincent L, Wright Andrew P, Halligan Brian, Chen Yanhua, Du Xiaomeng, Handelman Samuel K, Long Michelle T, Kiel Douglas P, Speliotes Elizabeth K
Division of Gastroenterology and Hepatology, Department of Medicine University of Michigan Health System Ann Arbor MI.
Department of Computational Medicine and Bioinformatics University of Michigan Medical School Ann Arbor MI.
Hepatol Commun. 2019 Jun 18;3(8):1073-1084. doi: 10.1002/hep4.1391. eCollection 2019 Aug.
Up to 25% of patients with nonalcoholic fatty liver disease (NAFLD) are not obese but may have a fat or muscle composition that predisposes them to NAFLD. Our aim was to determine whether body composition parameters associate with NAFLD and to identify genetic contributors to this association. This study included two cohorts. The first included 2,249 participants from the Framingham Heart Study who underwent a computed tomography scan to evaluate hepatic steatosis, dual-energy x-ray absorptiometry testing to assess body composition, and clinical examination. Body composition parameters were normalized to total body weight. A subset of participants underwent genotyping with an Affymetrix 550K single-nucleotide polymorphism array. The second cohort, Michigan Genomics Initiative, included 19,239 individuals with genotyping on the Illumina HumanCoreExome v.12.1 array and full electronic health record data. Using sex-stratified multivariable linear regression, greater central body fat associated with increased hepatic steatosis while greater lower extremity body fat associated with decreased hepatic steatosis. Greater appendicular lean mass was associated with decreased hepatic steatosis in men but not in women. A polygenic risk score for lipodystrophy (regional or global loss of adipose tissue) was associated with increased hepatic steatosis, increased liver fibrosis, and decreased lower extremity fat mass. Greater central body fat associated with increased hepatic steatosis, while greater lower extremity body fat and, in men, greater appendicular lean mass were associated with decreased hepatic steatosis. A genetic risk score for lipodystrophy was associated with NAFLD and liver fibrosis. Our results suggest that buffering of excess energy by peripheral fat and muscle may protect against NAFLD and liver fibrosis in the general population.
高达25%的非酒精性脂肪性肝病(NAFLD)患者并不肥胖,但可能具有使其易患NAFLD的脂肪或肌肉组成。我们的目的是确定身体成分参数是否与NAFLD相关,并识别这种关联的遗传因素。本研究包括两个队列。第一个队列包括来自弗雷明汉心脏研究的2249名参与者,他们接受了计算机断层扫描以评估肝脂肪变性、双能X线吸收法检测以评估身体成分以及临床检查。身体成分参数以总体重进行标准化。一部分参与者使用Affymetrix 550K单核苷酸多态性阵列进行基因分型。第二个队列是密歇根基因组计划,包括19239名在Illumina HumanCoreExome v.12.1阵列上进行基因分型并拥有完整电子健康记录数据的个体。使用按性别分层的多变量线性回归分析,较高的中心体脂肪与肝脂肪变性增加相关,而较高的下肢体脂肪与肝脂肪变性减少相关。较高的上肢瘦体重与男性肝脂肪变性减少相关,但与女性无关。脂肪营养不良(局部或全身性脂肪组织丢失)的多基因风险评分与肝脂肪变性增加、肝纤维化增加和下肢脂肪量减少相关。较高的中心体脂肪与肝脂肪变性增加相关,而较高的下肢体脂肪以及在男性中较高的上肢瘦体重与肝脂肪变性减少相关。脂肪营养不良的遗传风险评分与NAFLD和肝纤维化相关。我们的结果表明,外周脂肪和肌肉对多余能量的缓冲作用可能在一般人群中预防NAFLD和肝纤维化。