Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
Clin Gastroenterol Hepatol. 2023 Apr;21(4):931-939.e5. doi: 10.1016/j.cgh.2022.04.014. Epub 2022 May 2.
BACKGROUND & AIMS: Fibrosis is a key determinant of clinical outcomes in nonalcoholic fatty liver disease (NAFLD), but time-dependent risk of mortality has not been reported in previous meta-analyses. We performed an updated time-to-event meta-analysis to provide robust estimates for all-cause and liver-related mortality in biopsy-confirmed NAFLD with comparisons between fibrosis stages.
Medline and Embase databases were searched to include cohort studies reporting survival outcomes by fibrosis stage in biopsy-proven NAFLD. Survival estimates were pooled using reconstructed individual participant data. Conventional meta-analysis was conducted to pool adjusted hazard ratios (HRs) using DerSimonian and Laird random effects model.
A total of 14 articles involving 17,301 patients with NAFLD were included. All-cause mortality at 1, 5, and 10 years for stage 0 to 2 fibrosis was 0.1%, 3.3%, and 7.7% vs 0.3%, 20.6%, and 41.5% for stage 4 fibrosis. Compared with stage 0 fibrosis, all-cause mortality increased with fibrosis stage: stage 2; HR, 1.46 (95% confidence interval [CI], 1.08-1.98), stage 3; HR, 1.96 (95% CI, 1.41-2.72), and stage 4; HR, 3.66 (95% CI, 2.65-5.05). Risk for liver-related mortality increased exponentially as fibrosis stage increased: stage 2; HR, 4.07 (95% CI, 1.44-11.5), stage 3; HR, 7.59 (95% CI, 2.80-20.5), and stage 4; HR, 15.1 (95% CI, 5.27-43.4). Stage 3 to 4 fibrosis had a higher all-cause (HR, 3.32) and liver-related mortality (HR, 10.40) compared with stage 0 to 2 fibrosis, whereas stage 4 fibrosis had higher all-cause (HR, 2.67; 95% CI, 1.47-4.83) and liver-related mortality (HR, 2.57; 95% CI, 1.22-5.42) vs stage 3 fibrosis.
Risk of all-cause and liver-related mortality increases substantially with fibrosis stage. These data have important implications for prognostication and trial design.
纤维化是非酒精性脂肪性肝病(NAFLD)临床结局的关键决定因素,但之前的荟萃分析并未报告随时间变化的死亡率风险。我们进行了一项更新的时间事件荟萃分析,以提供活检证实的 NAFLD 纤维化分期之间比较的全因和肝脏相关死亡率的可靠估计。
检索 Medline 和 Embase 数据库,纳入了报告纤维化分期的活检证实的 NAFLD 患者生存结局的队列研究。使用重建的个体参与者数据汇总生存估计值。使用 DerSimonian 和 Laird 随机效应模型进行常规荟萃分析,以汇总调整后的风险比(HR)。
共纳入了 14 项涉及 17301 例 NAFLD 患者的研究。纤维化分期 0 至 2 级的全因死亡率在 1、5 和 10 年时分别为 0.1%、3.3%和 7.7%,而纤维化分期 4 级的全因死亡率分别为 0.3%、20.6%和 41.5%。与纤维化分期 0 级相比,全因死亡率随纤维化分期的增加而增加:分期 2 级 HR 为 1.46(95%可信区间 [CI],1.08-1.98),分期 3 级 HR 为 1.96(95%CI,1.41-2.72),分期 4 级 HR 为 3.66(95%CI,2.65-5.05)。肝脏相关死亡率的风险随纤维化分期的增加呈指数增加:分期 2 级 HR 为 4.07(95%CI,1.44-11.5),分期 3 级 HR 为 7.59(95%CI,2.80-20.5),分期 4 级 HR 为 15.1(95%CI,5.27-43.4)。与纤维化分期 0 至 2 级相比,纤维化分期 3 至 4 级的全因(HR,3.32)和肝脏相关死亡率(HR,10.40)更高,而纤维化分期 4 级的全因(HR,2.67;95%CI,1.47-4.83)和肝脏相关死亡率(HR,2.57;95%CI,1.22-5.42)均高于纤维化分期 3 级。
全因和肝脏相关死亡率的风险随纤维化分期显著增加。这些数据对预后和试验设计具有重要意义。