Division of Gastroenterology and Hepatology, Department of Medicine, University of California-San Francisco, San Francisco, CA.
Division of Transplant Surgery, Department of Surgery, University of California-San Francisco, San Francisco, CA.
J Hepatol. 2020 Sep;73(3):575-581. doi: 10.1016/j.jhep.2020.03.029. Epub 2020 Mar 30.
BACKGROUND & AIMS: To date, studies evaluating the association between frailty and mortality in patients with cirrhosis have been limited to assessments of frailty at a single time point. We aimed to evaluate changes in frailty over time and their association with death/delisting in patients too sick for liver transplantation.
Adults with cirrhosis, listed for liver transplantation at 8 US centers, underwent ambulatory longitudinal frailty testing using the liver frailty index (LFI). We used multilevel linear mixed-effects regression to model and predict changes in LFI (ΔLFI) per 3 months, based on age, gender, model for end-stage liver disease (MELD)-Na, ascites, and hepatic encephalopathy, categorizing patients by frailty trajectories. Competing risk regression evaluated the subhazard ratio (sHR) of baseline LFI and predicted ΔLFI on death/delisting, with transplantation as the competing risk.
We analyzed 2,851 visits from 1,093 outpatients with cirrhosis. Patients with severe worsening of frailty had worse baseline LFI and were more likely to have non-alcoholic fatty liver disease, diabetes, or dialysis-dependence. After a median follow-up of 11 months, 223 (20%) of the overall cohort died/were delisted because of sickness. The cumulative incidence of death/delisting increased by worsening ΔLFI group. In competing risk regression adjusted for baseline LFI, age, height, MELD-Na, and albumin, a 0.1 unit change in ΔLFI per 3 months was associated with a 2.04-fold increased risk of death/delisting (95% CI 1.35-3.09).
Worsening frailty was significantly associated with death/delisting independent of baseline frailty and MELD-Na. Notably, patients who experienced improvements in frailty had a lower risk of death/delisting. Our data support the longitudinal measurement of frailty, using the LFI, in patients with cirrhosis and lay the foundation for interventional work aimed at reversing frailty.
Frailty, as measured at a single time point, is predictive of death in patients with cirrhosis, but whether changes in frailty over time are associated with death is unknown. In a study of over 1,000 patients with cirrhosis who underwent frailty testing, we demonstrate that worsening frailty is strongly linked with mortality, regardless of baseline frailty and liver disease severity. Notably, patients who experienced improvements in frailty over time had a lower risk of death/delisting. Our data support the longitudinal measurement of frailty in patients with cirrhosis and lay the foundation for interventional work aimed at reversing frailty.
迄今为止,评估肝硬化患者衰弱与死亡率之间关联的研究仅限于单次评估衰弱情况。我们旨在评估衰弱随时间的变化及其与不适于进行肝移植的患者死亡/退出的关系。
8 家美国中心的肝移植候选者中,患有肝硬化的成年人接受了使用肝衰弱指数(LFI)的门诊纵向衰弱测试。我们使用多级线性混合效应回归来基于年龄、性别、终末期肝病模型(MELD)-Na、腹水和肝性脑病,对每 3 个月的 LFI(ΔLFI)变化进行建模和预测,根据衰弱轨迹对患者进行分类。竞争风险回归评估基线 LFI 和预测的ΔLFI 对死亡/退出的亚危险比(sHR),以移植为竞争风险。
我们分析了来自 1093 名门诊患者的 2851 次就诊。严重衰弱恶化的患者基线 LFI 较差,且更有可能患有非酒精性脂肪性肝病、糖尿病或透析依赖。在中位随访 11 个月后,整体队列中有 223 名(20%)因疾病而死亡/被取消资格。随着ΔLFI 恶化组的累积发病率增加,死亡/退出的累积发生率增加。在调整基线 LFI、年龄、身高、MELD-Na 和白蛋白的竞争风险回归中,每 3 个月 LFI 变化 0.1 个单位与死亡/退出的风险增加 2.04 倍(95%CI 1.35-3.09)相关。
衰弱恶化与死亡/退出显著相关,与基线衰弱和 MELD-Na 无关。值得注意的是,衰弱改善的患者死亡/退出的风险较低。我们的数据支持使用 LFI 对肝硬化患者进行衰弱的纵向测量,并为旨在逆转衰弱的干预工作奠定了基础。
非专业人士请谨慎阅读