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2019-2030 年加拿大非酒精性脂肪性肝病负担:建模研究。

Burden of nonalcoholic fatty liver disease in Canada, 2019-2030: a modelling study.

机构信息

Division of Gastroenterology and Hepatology (Swain, Shaheen), Cumming School of Medicine, University of Calgary, Calgary, Alta.; Division of Gastroenterology (Ramji), University of British Columbia, Vancouver, BC; Toronto Centre for Liver Disease (Patel), University Hospital Network, Toronto, Ont.; Division of Gastroenterology and Hepatology (Sebastiani), McGill University Health Centre, Montréal, Que.; LAIR Centre (Tam), Vancouver, BC; Division of Gastroenterology (Marotta), Department of Medicine, Schulich School of Medicine and Dentistry, University of Western Ontario, London, Ont.; Toronto Liver Centre (Elkhashab), Toronto, Ont.; LMC Diabetes and Endocrinology Brampton (Bajaj), Brampton, Ont.; Leadership Sinai Centre for Diabetes (Bajaj), Mount Sinai Hospital, Toronto, Ont.; Center for Disease Analysis Foundation (Estes, Razavi), Lafayette, Colo.

出版信息

CMAJ Open. 2020 Jun 9;8(2):E429-E436. doi: 10.9778/cmajo.20190212. Print 2020 Apr-Jun.

Abstract

BACKGROUND

Nonalcoholic fatty liver disease (NAFLD) and nonalcoholic steatohepatitis (NASH) account for a growing proportion of liver disease cases, and there is a need to better understand future disease burden. We used a modelling framework to forecast the burden of disease of NAFLD and NASH for Canada.

METHODS

We used a Markov model to forecast fibrosis progression from stage F0 (no fibrosis) to stage F4 (compensated cirrhosis) and subsequent progression to decompensated cirrhosis, hepatocellular carcinoma, liver transplantation and liver-related death among Canadians with NAFLD from 2019 to 2030. We used historical trends for obesity prevalence among adults to estimate longitudinal changes in the number of incident NAFLD cases.

RESULTS

The model projected that the number of NAFLD cases would increase by 20% between 2019 and 2030, from an estimated 7 757 000 cases to 9 305 000 cases. Increases in advanced fibrosis cases were relatively greater, as the number of model-estimated prevalent stage F3 cases would increase by 65%, to 357 000, and that of prevalent stage F4 cases would increase by 95%, to 195 000. Estimated incident cases of hepatocellular carcinoma and decompensated cirrhosis would increase by up to 95%, and the number of annual NAFLD-related deaths would double, to 5600.

INTERPRETATION

Increasing rates of obesity translate into increasing NAFLD-related cases of cirrhosis and hepatocellular carcinoma and related mortality. Prevention efforts should be aimed at reducing the incidence of NAFLD and slowing fibrosis progression among those already affected.

摘要

背景

非酒精性脂肪性肝病(NAFLD)和非酒精性脂肪性肝炎(NASH)在肝病病例中所占比例不断增加,因此需要更好地了解未来的疾病负担。我们使用建模框架预测加拿大的 NAFLD 和 NASH 疾病负担。

方法

我们使用马尔可夫模型来预测 2019 年至 2030 年期间加拿大 NAFLD 患者从无纤维化(F0 期)进展为纤维化 F4 期(代偿性肝硬化)及随后进展为失代偿性肝硬化、肝细胞癌、肝移植和与肝脏相关死亡的疾病进展情况。我们使用成年人肥胖患病率的历史趋势来估计新发 NAFLD 病例数量的纵向变化。

结果

该模型预测,2019 年至 2030 年期间,NAFLD 病例数将增加 20%,预计从 775.7 万例增加至 930.5 万例。进展性纤维化病例的增加相对更为显著,因为模型估计的 F3 期现患病例数将增加 65%,达到 35.7 万例,F4 期现患病例数将增加 95%,达到 19.5 万例。肝细胞癌和失代偿性肝硬化的估计新发病例数将增加 95%,每年与 NAFLD 相关的死亡人数将增加一倍,达到 5600 人。

结论

肥胖率的上升导致与 NAFLD 相关的肝硬化和肝细胞癌病例以及相关死亡率增加。预防措施应旨在降低 NAFLD 的发病率并减缓已经受影响人群的纤维化进展。

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