作者
Elina Cho,C. Ang,Jingxuan Quek,Clarissa Elysia Fu,Lincoln Kai En Lim,Zane En Qi Heng,Darren Jun Hao Tan,Wen Hui Lim,Jie Ning Yong,Rebecca Wenling Zeng,Douglas Chee,Benjamin Nah,Cosmas Rinaldi Adithya Lesmana,Aung Hlaing Bwa,Khin Maung Win,Claire Faulkner,Majd B. Aboona,Mei Chin Lim,Nicholas Syn,Anand V. Kulkarni,Hiroyuki Suzuki,Hirokazu Takahashi,Nobuharu Tamaki,Karn Wijarnpreecha,Daniel Q. Huang,Mark Muthiah,Cheng Han Ng,Rohit Loomba
摘要
Non-alcoholic fatty liver disease (NAFLD) is the leading cause of chronic liver disease, with type 2 diabetes mellitus (T2DM) as a major predictor. Insulin resistance and chronic inflammation are key pathways in the pathogenesis of T2DM leading to NAFLD and vice versa, with the synergistic effect of NAFLD and T2DM increasing morbidity and mortality risks. This meta-analysis aims to quantify the prevalence of NAFLD and the prevalence of clinically significant and advanced fibrosis in people with T2DM.MEDLINE and Embase databases were searched from inception until 13 February 2023. The primary outcomes were the prevalence of NAFLD, non-alcoholic steatohepatitis (NASH) and fibrosis in people with T2DM. A generalised linear mixed model with Clopper-Pearson intervals was used for the analysis of proportions with sensitivity analysis conducted to explore heterogeneity between studies.156 studies met the inclusion criteria, and a pooled analysis of 1 832 125 patients determined that the prevalence rates of NAFLD and NASH in T2DM were 65.04% (95% CI 61.79% to 68.15%, I2=99.90%) and 31.55% (95% CI 17.12% to 50.70%, I2=97.70%), respectively. 35.54% (95% CI 19.56% to 55.56%, I2=100.00%) of individuals with T2DM with NAFLD had clinically significant fibrosis (F2-F4), while 14.95% (95% CI 11.03% to 19.95%, I2=99.00%) had advanced fibrosis (F3-F4).This study determined a high prevalence of NAFLD, NASH and fibrosis in people with T2DM. Increased efforts are required to prevent T2DM to combat the rising burden of NAFLD.CRD42022360251.