The relationship between frailty and cirrhosis etiology: From the Functional Assessment in Liver Transplantation (FrAILT) Study. (14th July 2021)

• Record Type: Journal Article
• Authors: Xu, Chelsea Q.; Mohamad, Yara; Kappus, Matthew R.; Boyarsky, Brian; Ganger, Daniel R.; Volk, Michael L.; Rahimi, Robert S.; Duarte‐Rojo, Andres; McAdams‐DeMarco, Mara; Segev, Dorry L.; Ladner, Daniela P.; Verna, Elizabeth C.; Grab, Joshua; Tincopa, Monica; Dunn, Michael A.; Lai, Jennifer C.
• Is Part Of: Liver international. Volume 41:Number 10(2021)
• Page Start: 2467
• Page End: 2473
• Publication Date: 2021-07-14
• Subjects: frailty -- malnutrition -- NAFLD -- non‐alcoholic fatty liver disease -- physical function -- sarcopenia; Liver -- Periodicals; Liver -- Diseases -- Periodicals; 616.362
• DOI: 10.1111/liv.15006
• Languages: English
• ISSNs: 1478-3223

Abstract

Abstract: Background & Aims: Cirrhosis leads to malnutrition and muscle wasting that manifests as frailty, which may be influenced by cirrhosis aetiology. We aimed to characterize the relationship between frailty and cirrhosis aetiology. Methods: Included were adults with cirrhosis listed for liver transplantation (LT) at 10 US centrer who underwent ambulatory testing with the Liver Frailty Index (LFI; 'frail' = LFI ≥ 4.4). We used logistic regression to associate aetiologies and frailty, and competing risk regression (LT as the competing risk) to determine associations with waitlist mortality (death/delisting for sickness). Results: Of 1, 623 patients, rates of frailty differed by aetiology: 22% in chronic hepatitis C, 31% in alcohol‐associated liver disease (ALD), 32% in non‐alcoholic fatty liver disease (NAFLD), 21% in autoimmune/cholestatic and 31% in 'other' ( P < .001). In univariable logistic regression, ALD (OR 1.53, 95% CI 1.12‐2.09), NAFLD (OR 1.64, 95% CI 1.18‐2.29) and 'other' (OR 1.58, 95% CI 1.06‐2.36) were associated with frailty. In multivariable logistic regression, only ALD (OR 1.40; 95% 1.01‐1.94) and 'other' (OR 1.59; 95% 1.05‐2.40) remained associated with frailty. A total of 281 (17%) patients died/were delisted for sickness. In multivariable competing risk regression, LFI was associated with waitlist mortality (sHR 1.05, 95% CI 1.03‐1.06), but aetiology was not ( P > .05 for each). No interaction between frailty and aetiology on the association with waitlist mortality was found ( P > .05 for each interaction term). Conclusions: Frailty is more common in patients with ALD, NAFLD and 'other' aetiologies. However, frailty was associated with waitlist mortality independent of cirrhosis aetiology, supporting the applicability of frailty across all cirrhosis aetiologies.