Wallace Carolyn, Gamkrelidze Ivane, Estes Chris, Razavi Homie, Sanyal Arun J
Center for Disease Analysis Foundation, Lafayette, Colorado, USA.
Center for Disease Analysis Foundation, Lafayette, Colorado, USA.
J Hepatol. 2025 Jan 18. doi: 10.1016/j.jhep.2025.01.009.
BACKGROUND & AIMS: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a common condition leading to chronic liver disease which generates substantial healthcare costs. Our aim was to model the impact of a hypothetical pharmacologic therapy which halts MASLD fibrosis progression on disease and economic burden.
The US MASLD disease burden model is a Markov model which forecasts disease progression and the impact of diagnosis and treatment. Diagnostic costs for all patients and direct costs for patients with MASLD-related liver disease were also incorporated. MASLD disease burden and economic impacts were modeled for five scenarios: a no treatment case and four interventions incorporating the impact of gradually increasing awareness, screening, and diagnosis, and treatment with anti-steatotic therapy and a future, hypothetical therapy that halts fibrosis progression.
Treatment with therapy which only reverses steatosis had minimal (<1 to 2%) effect on cumulative chronic liver disease cases and healthcare costs averted. The scenarios in which a hypothetical therapy halts fibrosis progression resulted in reductions in cases of decompensated cirrhosis (11-39%), hepatocellular carcinoma (10-34%), and liver-related deaths (8-31%), a 9-31% reduction in cumulative DALYs, and $40.5 to $99.1B incremental healthcare costs averted.
Increasing diagnosis and treatment for the MASLD population with moderate-to-advanced fibrosis will prevent advanced liver disease and death and will result in reducing the associated direct healthcare costs. Increasing awareness, screening and diagnosis along with introducing pharmacologic therapies that halt fibrosis progression are necessary to realize health and economic benefits for the MASLD population.
Metabolic dysfunction-associated steatotic liver disease (MASLD), the most rapidly increasing and prevalent cause of chronic liver disease, is associated with substantial healthcare costs. As disease burden and costs mount, pharmacologic therapy which halts MASLD fibrosis progression is coming to fruition. Modeling the impact on disease progression of a hypothetical pharmacologic therapy which halts MASLD fibrosis progression through multiple scenarios provides insights into the key drivers of the disease and costs associated with it. This should help to facilitate best policies and practices to mitigate the burden of MASLD.
代谢功能障碍相关脂肪性肝病(MASLD)是导致慢性肝病的常见病症,会产生高昂的医疗费用。我们的目的是建立一个假设的药物治疗模型,该治疗可阻止MASLD纤维化进展,评估其对疾病和经济负担的影响。
美国MASLD疾病负担模型是一个马尔可夫模型,用于预测疾病进展以及诊断和治疗的影响。还纳入了所有患者的诊断成本和与MASLD相关肝病患者的直接成本。针对五种情况对MASLD疾病负担和经济影响进行建模:一种是不治疗的情况,以及四种干预措施,包括逐渐提高认知、筛查、诊断的影响,采用抗脂肪变性疗法进行治疗,以及一种未来可阻止纤维化进展的假设疗法。
仅逆转脂肪变性的治疗对累积慢性肝病病例和避免的医疗费用影响极小(<1%至2%)。假设疗法可阻止纤维化进展的情况导致失代偿性肝硬化病例减少(11% - 39%)、肝细胞癌减少(10% - 34%)、肝相关死亡减少(8% - 31%),累积伤残调整生命年减少9% - 31%,避免的医疗费用增量为405亿至991亿美元。
对中重度纤维化的MASLD患者增加诊断和治疗将预防晚期肝病和死亡,并降低相关的直接医疗费用。提高认知、筛查和诊断水平,同时引入可阻止纤维化进展的药物治疗,对于实现MASLD患者的健康和经济效益是必要的。
代谢功能障碍相关脂肪性肝病(MASLD)是慢性肝病中增长最快且最普遍的病因,与高昂的医疗费用相关。随着疾病负担和成本的增加,可阻止MASLD纤维化进展的药物治疗即将实现。通过多种情况对可阻止MASLD纤维化进展的假设药物治疗对疾病进展的影响进行建模,可为该疾病的关键驱动因素及其相关成本提供见解。这应有助于促进最佳政策和实践,以减轻MASLD的负担。