Tai Chi-Ming, Huang Chih-Kun, Tu Hung-Pin, Hwang Jau-Chung, Yeh Ming-Lun, Huang Chung-Feng, Huang Jee-Fu, Dai Chia-Yen, Chuang Wan-Long, Yu Ming-Lung
From the Institute of Clinical Medicine, College of Medicine, Kaohsiung Medical University (C-MT, C-FH, J-FH, C-YD, W-LC, M-LY); Department of Internal Medicine (C-MT); Department of Bariatric and Metabolic International Surgery Center, E-Da Hospital, I-Shou University (C-MT, C-KH); Department of Public Health and Environmental Medicine, School of Medicine, College of Medicine, Kaohsiung Medical University, Kaohsiung (H-PT); Department of Pathology, Lin Shin Hospital, Taichung (J-CH); Hepatobiliary Division, Department of Internal Medicine and Hepatitis Center, Kaohsiung Medical University Hospital, Kaohsiung (M-LY, C-FH, J-FH, C-YD, W-LC, M-LY); Faculty of Internal Medicine, School of Medicine, College of Medicine, and Lipid Science and Aging Research Center, and Center for Infectious Disease and Cancer Research, Kaohsiung Medical University (M-LY); and Institute of Biomedical Sciences, National Sun Yat-Sen University, Kaohsiung, Taiwan (M-LY).
Medicine (Baltimore). 2016 Mar;95(12):e3120. doi: 10.1097/MD.0000000000003120.
The patatin-like phospholipase domain-containing protein 3 (PNPLA3) variant is associated with nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH). However, the role of genetic variations of the peroxisome proliferator-activated receptor gamma coactivator-1-alpha gene (PPARGC1A) and glucokinase regulatory (GCKR) gene on NASH in obese patients remains unclear. We studied the effects and interaction of these genetic polymorphisms on NASH in severely obese Taiwanese patients.The genotypes of PPARGC1A rs8192678, PNPLA3 rs738409, and GCKR rs780094 were determined in 177 severely obese patients who underwent bariatric surgery. NASH was evaluated by liver histopathology.Of 177 patients, 29 (16.4%), 57 (33.2%), and 91 (51.4%) were in the non-NAFLD, steatosis, and NASH groups, respectively. We found that the PPARGC1A and PNPLA3 variants, but not the GCKR variant, were associated with NASH. The PPARGC1A rs8192678 GA/AA genotype was associated with higher steatosis grade and presence of ballooning degeneration. The PNPLA3 rs738409 GG genotype was associated with higher severity in all histologic features except for fibrosis. In multivariate analysis, both the PPARGC1A rs8192678 GA/AA genotype (odds ratio [OR] 2.32; 95% confidence interval [CI] 1.08-4.98; P = 0.031) and the PNPLA3 rs738409 GG genotype (OR 4.05; 95% CI 1.24-13.23; P = 0.021), and also body mass index were independent risk factors for NASH. Further, there was an additive effect of the PPARGC1A rs8192678 GA/AA genotype and the PNPLA3 rs738409 GG genotype on the presence of NASH (OR 6.83; 95% CI 1.61-29.01; P = 0.009).The PPARGC1A rs8192678 GA/AA genotype and the PNPLA3 rs738409 GG genotype had an additive effect on NASH in severely obese Taiwanese patients.
含patatin样磷脂酶结构域蛋白3(PNPLA3)变体与非酒精性脂肪性肝病(NAFLD)和非酒精性脂肪性肝炎(NASH)相关。然而,过氧化物酶体增殖物激活受体γ辅激活因子-1α基因(PPARGC1A)和葡萄糖激酶调节(GCKR)基因的遗传变异对肥胖患者NASH的作用仍不清楚。我们研究了这些基因多态性对重度肥胖台湾患者NASH的影响及相互作用。在177例接受减肥手术的重度肥胖患者中测定了PPARGC1A rs8192678、PNPLA3 rs738409和GCKR rs780094的基因型。通过肝脏组织病理学评估NASH。177例患者中,非NAFLD、脂肪变性和NASH组分别有29例(16.4%)、57例(33.2%)和91例(51.4%)。我们发现PPARGC1A和PNPLA3变体与NASH相关,但GCKR变体与NASH无关。PPARGC1A rs8192678 GA/AA基因型与更高的脂肪变性分级和气球样变性的存在相关。PNPLA3 rs738409 GG基因型与除纤维化外的所有组织学特征的更高严重程度相关。在多变量分析中,PPARGC1A rs8192678 GA/AA基因型(比值比[OR] 2.32;95%置信区间[CI] 1.08 - 4.98;P = 0.031)和PNPLA3 rs738409 GG基因型(OR 4.05;95% CI 1.24 - 13.23;P = 0.021)以及体重指数都是NASH的独立危险因素。此外,PPARGC1A rs8192678 GA/AA基因型和PNPLA3 rs738409 GG基因型对NASH的存在有相加作用(OR 6.83;95% CI 1.61 - 29.01;P = 0.009)。PPARGC1A rs8192678 GA/AA基因型和PNPLA3 rs738409 GG基因型对重度肥胖台湾患者的NASH有相加作用。