Njei Basile, Mezzacappa Catherine, John Binu V, Serper Marina, Kaplan David E, Taddei Tamar H, Mahmud Nadim
Section of Digestive Diseases, Yale University School of Medicine/VA Connecticut Healthcare System, New Haven, CT, USA.
University of Miami and Miami VA Health System, Miami, FL, USA.
Dig Dis Sci. 2025 Feb;70(2):802-813. doi: 10.1007/s10620-024-08764-4. Epub 2025 Jan 8.
Metabolic dysfunction-associated steatotic liver disease (MASLD) has a global prevalence of 25%. Studies on incident liver and cardiovascular outcomes in lean (Body mass index: BMI < 25 kg/m, or < 23 kg/m for Asians) vs. non-lean individuals with MASLD have reported mixed results. We aimed to compare incident clinical outcomes and mortality between lean and non-lean individuals with compensated MASLD cirrhosis in a large national cohort.
This was a retrospective cohort study of patients with newly diagnosed compensated MASLD cirrhosis in the Veterans Health Administration between 01/2008 and 05/2021. The primary outcome was incident hepatic decompensation, and secondary outcomes were incident major adverse cardiovascular events (MACE) and all-cause mortality. Multivariable Cox proportional hazard models were used to assess association. Fine and Gray competing risk regression was used where applicable.
The study included 15155 patients with MASLD cirrhosis: 1,597 lean and 13558 non-lean patients. Included patients were mostly male (95%), median age was 67 years, and 72.8% were non-Hispanic white. At baseline, the prevalence of diabetes was lower in lean vs. non-lean individuals (46.7 vs. 73.9%, p < 0.001). In multivariable models, lean status was associated with a 64% increased risk of all-cause mortality (aHR = 1.64) but decreased risk of hepatic decompensation (aSHR = 0.67). Lean individuals experienced significantly higher rates of cardiovascular-related mortality (aHR = 1.40).
Lean MASLD patients with compensated cirrhosis had a higher mortality risk but a lower risk of hepatic decompensation than non-lean patients. Despite having a better baseline cardiometabolic profile and similar rates of MACE, lean individuals with MASLD cirrhosis have a higher risk of cardiovascular mortality.
代谢功能障碍相关脂肪性肝病(MASLD)在全球的患病率为25%。关于瘦型(体重指数:BMI<25kg/m²,亚洲人为<23kg/m²)与非瘦型MASLD患者肝脏和心血管事件发生率的研究结果不一。我们旨在比较一个大型全国队列中瘦型与非瘦型代偿期MASLD肝硬化患者的临床事件发生率和死亡率。
这是一项对2008年1月至2021年5月期间退伍军人健康管理局新诊断的代偿期MASLD肝硬化患者进行的回顾性队列研究。主要结局是发生肝失代偿,次要结局是发生主要不良心血管事件(MACE)和全因死亡率。采用多变量Cox比例风险模型评估相关性。在适用的情况下使用Fine和Gray竞争风险回归模型。
该研究纳入了15155例MASLD肝硬化患者:1597例瘦型患者和13558例非瘦型患者。纳入的患者大多为男性(95%),中位年龄为67岁,72.8%为非西班牙裔白人。在基线时,瘦型个体的糖尿病患病率低于非瘦型个体(46.7%对73.9%,p<0.001)。在多变量模型中,瘦型状态与全因死亡率风险增加64%相关(调整后风险比[aHR]=1.64),但肝失代偿风险降低(调整后亚分布风险比[aSHR]=0.67)。瘦型个体的心血管相关死亡率显著更高(aHR=1.40)。
代偿期肝硬化的瘦型MASLD患者比非瘦型患者有更高的死亡风险,但肝失代偿风险更低。尽管瘦型MASLD肝硬化患者的基线心脏代谢状况较好且MACE发生率相似,但其心血管死亡风险更高。