Department of Gastroenterology, National Clinical Research Center for Digestive Disease, Beijing Friendship Hospital, Capital Medical University, Beijing Digestive Disease Center, Beijing Key Laboratory for Precancerous Lesion of Digestive Disease, Beijing, China.
Clinical Epidemiology and EBM Unit, National Clinical Research Center for Digestive Disease, Beijing Friendship Hospital, Capital Medical University, Beijing, China.
Front Endocrinol (Lausanne). 2021 May 13;12:657856. doi: 10.3389/fendo.2021.657856. eCollection 2021.
Obesity has been demonstrated to show a consistent link with the increased possibility of nonalcoholic fatty liver disease (NAFLD). Since both serum uric acid (SUA) and obesity are essential components of metabolic syndrome (MetS), it is uncertain whether the incidence of NAFLD results from serum uric acid, obesity, or other potential factors based on previous studies.
This study enrolled 16,839 participants with no history of alcohol consumption and no fatty liver disease in 2010. All participants completed a survey which included health and lifestyle questionnaires, and underwent physical examination, ultrasonography, and laboratory examinations of blood samples. After the four-year follow up, 5,104 (30.31%) participants were diagnosed with NAFLD. The associations between SUA, BMI or obesity, and incident NAFLD were assessed by multivariate linear regression, logistic regression analysis, and mediation analysis, respectively.
By adjusting demographic and serum characteristics, linear correlation coefficients between obesity and SUA were 20.26 [95% confidence interval (CI)]: 15.74, 24.77), 13.31 (95% CI: 6.63, 19.99) and 22.21 (95% CI: 16.41, 28.02) in the total population, and in the female and male groups, respectively. The odds ratios were 2.49 (95% CI: 1.61, 3.87) in the total population, 5.71 (95% CI: 2.25, 14.45) in the female group and 1.99 (95% CI: 1.15, 3.45) in the male group for the correlation between obesity and incident NAFLD. The mediation analysis showed that SUA contributed to 10.03%, 0.58%, and 12.54% of obesity-related NAFLD development in the total population, females and males, respectively.
The findings showed mediation linkages of both obesity and SUA with the incident NAFLD. The role of SUA as a mediator constitutes clinical significance that should be recognized and considered.
肥胖与非酒精性脂肪性肝病(NAFLD)的发生几率增加密切相关。由于血清尿酸(SUA)和肥胖均为代谢综合征(MetS)的重要组成部分,因此根据既往研究结果,尚不确定 NAFLD 的发生是否源于血清尿酸、肥胖或其他潜在因素。
本研究共纳入 16839 例 2010 年无饮酒史且无脂肪肝病史的参与者。所有参与者均完成了一份健康和生活方式调查问卷,并接受了体格检查、超声检查以及血液样本实验室检查。经过 4 年的随访,5104 例(30.31%)参与者被诊断为 NAFLD。采用多元线性回归、logistic 回归分析和中介分析分别评估了 SUA、BMI 或肥胖与新发 NAFLD 之间的关系。
在调整人口统计学和血清特征后,肥胖与 SUA 之间的线性相关系数在总人群中分别为 20.26(95%置信区间:15.74,24.77)、13.31(95%置信区间:6.63,19.99)和 22.21(95%置信区间:16.41,28.02),在女性和男性群体中,肥胖与 SUA 之间的相关系数分别为 22.21(95%置信区间:16.41,28.02)、13.31(95%置信区间:6.63,19.99)和 20.26(95%置信区间:15.74,24.77)。总人群中肥胖与新发 NAFLD 的比值比为 2.49(95%置信区间:1.61,3.87),女性组为 5.71(95%置信区间:2.25,14.45),男性组为 1.99(95%置信区间:1.15,3.45)。中介分析显示,SUA 导致肥胖相关 NAFLD 发展的比例分别为总人群中的 10.03%、女性组中的 0.58%和男性组中的 12.54%。
本研究结果表明肥胖和 SUA 与新发 NAFLD 之间存在中介关系。SUA 作为一种中介物具有重要的临床意义,值得进一步认识和考虑。