Department of Cardiology, The Second Xiangya Hospital, Central South University, 139 Middle Renmin Road, Changsha, 410011, China.
National Key Laboratory of Human Factors Engineering, 1 west Yuanmin Yuan Road, Beijing, 100094, China.
Lipids Health Dis. 2020 Feb 4;19(1):18. doi: 10.1186/s12944-020-1201-6.
Non-alcoholic fatty liver disease (NAFLD) is currently the major cause of chronic liver disease globally. Bile acids (BAs) have emerged as relevant signaling molecules that are associated with NAFLD development. This study was aimed to examine the association of serum total bile acids (TBAs) with NAFLD in a large population of Chinese subjects.
This cross sectional study recruited 152,336 participants from the Second Xiangya Hospital, China. NAFLD was diagnosed based on the presence of hepatic steatosis on ultrasonography, without significant alcohol consumption and other known causes for chronic liver disease. A multivariate logistic regression model was used to test for the association of serum TBAs with NAFLD, adjusting for conventional risk factors of NAFLD.
A total of 27.4% of the participants had NAFLD. Patients with NAFLD had slightly higher TBA levels than those without, 3.4 vs. 3.0 μmol/L (p < 0.001). However, TBA levels were not associated with NAFLD in the multivariate logistic regression model, which adjusted for age, gender and other acknowledged risk factors for NAFLD (OR = 1.00. 95% CI: 1.00-1.00, p = 0.797).
We found that the serum TBA levels were not associated with NAFLD. Future studies in a large population, focusing on serum BA composition may improve the understating of the role of BAs in NAFLD.
非酒精性脂肪性肝病(NAFLD)是目前全球慢性肝病的主要病因。胆汁酸(BAs)已成为与 NAFLD 发展相关的重要信号分子。本研究旨在检查中国人群中血清总胆汁酸(TBAs)与 NAFLD 的相关性。
本横断面研究共纳入来自中国湘雅二医院的 152336 名参与者。根据超声检查存在肝脂肪变性、无明显饮酒和其他已知慢性肝病病因诊断为 NAFLD。采用多变量 logistic 回归模型,在调整 NAFLD 的常规危险因素后,检验血清 TBAs 与 NAFLD 的相关性。
共有 27.4%的参与者患有 NAFLD。与无 NAFLD 者相比,NAFLD 患者的 TBA 水平略高,分别为 3.4μmol/L 和 3.0μmol/L(p<0.001)。然而,在调整年龄、性别和其他公认的 NAFLD 危险因素的多变量 logistic 回归模型中,TBA 水平与 NAFLD 无关(OR=1.00,95%CI:1.00-1.00,p=0.797)。
我们发现血清 TBA 水平与 NAFLD 无关。未来在更大人群中,针对血清 BA 组成的研究可能会提高对 BAs 在 NAFLD 中作用的认识。