# Screening for Malnutrition, Sarcopenia, and Physical Frailty Beyond One Year after Liver Transplantation

**Authors:** Amal Trigui, Crystèle Hogue, Mélanie Tremblay, Geneviève Huard, Christopher F. Rose, Chantal Bémeur

PMC · DOI: 10.1016/j.jceh.2025.103421 · Journal of Clinical and Experimental Hepatology · 2025-11-29

## TL;DR

This study found that liver transplant patients remain at risk for malnutrition, sarcopenia, and frailty up to three years post-transplant, emphasizing the need for long-term care.

## Contribution

The study provides novel long-term follow-up data on malnutrition, sarcopenia, and frailty risks beyond one year after liver transplantation.

## Key findings

- Malnutrition, sarcopenia, and frailty risks remained stable up to three years post-transplant.
- Energy intake and muscle function were significant predictors of malnutrition and sarcopenia.
- Only a minority of patients returned to work within three years after liver transplantation.

## Abstract

Malnutrition, sarcopenia, and frailty negatively impact quality of life and increase mortality following liver transplantation (LT). However, long-term follow-up data remain limited. This study aimed primarily to assess the malnutrition risk at 1-, 2-, and 3-years post-LT. Secondary objectives included evaluating the sarcopenia and frailty risk, muscle function, physical activity, quality of life, and employment status at the same time points.

This cross-sectional study included LT recipients with a history of cirrhosis, transplanted between January 2019 and December 2021. Each participant completed a single virtual meeting during which nutritional risk, sarcopenia, frailty risk, muscle function, physical activity, quality of life, employment status, and dietary intakes were assessed.

Sixty-six LT recipients (63.6% male) were included: cohort A (1-year post-LT, n = 25), cohort B (2 years post-LT, n = 14), and cohort C (3 years post-LT, n = 27). The prevalence of malnutrition (12.0%, 14.3%, and 11.1%), sarcopenia (16.0%, 28.6%, and 18.5%), and frailty risks (12.0%, 28.6%, and 18.5%) in cohorts A, B, and C, respectively, remained stable over time (P = 0.957, 0.626, and 0.436). Energy intake was a significant predictor of both malnutrition and sarcopenia, with muscle function predicting the risk of sarcopenia and frailty post-LT. Muscle function was lowest in cohort B and inferior in age-matched adults in all cohorts. One-third of patients had low physical activity levels, with no significant change across cohorts (P = 0.096). Quality of life remained unchanged, except for lower emotional well-being and health change scores in cohort C compared to cohort A (P = 0.039 and P < 0.001, respectively). Only 28.0%, 42.9%, and 25.9% of participants in cohorts A, B, and C, respectively, returned to work.

Up to 3 years after LT, patients were still at risk of malnutrition, sarcopenia, and frailty. The results of this study highlight the need for targeted interventions to improve outcomes and support long-term quality of life post-LT.

## Linked entities

- **Diseases:** cirrhosis (MONDO:0005155), malnutrition (MONDO:0006873)

## Full-text entities

- **Genes:** MSTN (myostatin) [NCBI Gene 2660] {aka GDF8, MSLHP}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, CST12P (cystatin 12, pseudogene) [NCBI Gene 106478911] {aka Cst, Ctes4, E2}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** cholestatic (MESH:D002779), PSC (MESH:D015209), type II muscle fiber atrophy (MESH:D009133), loss of muscle function (MESH:D009135), fatigue (MESH:D005221), type 2 diabetes (MESH:D003924), end-stage liver disease (MESH:D058625), cancer (MESH:D009369), CHC (MESH:D006528), Cirrhosis (MESH:D005355), Sarcopenia (MESH:D055948), orthopedic complications (MESH:D009140), LT (MESH:D017093), hypertension (MESH:D006973), PBC (MESH:D008105), obesity (MESH:D009765), loss of muscle mass (MESH:C536030), Frailty (MESH:D000073496), alcoholic cirrhosis (MESH:D008104), infections (MESH:D007239), dyslipidemia (MESH:D050171), renal dysfunction (MESH:D007674), renal (MESH:D006030), non-alcoholic steato-hepatitis (MESH:D006519), pain (MESH:D010146), chronic renal failure (MESH:D007676), muscle hypertrophy (MESH:C536106), MA (MESH:C565640), chronic kidney disease (MESH:D051436), Malnutrition (MESH:D044342), cardiovascular disease (MESH:D002318), death (MESH:D003643), VA (MESH:C563443), biliary complications (MESH:D008107), overweight (MESH:D050177), weight loss (MESH:D015431), fulminant hepatitis (MESH:D017114), protein-calorie malnutrition (MESH:D011502), Diabetes (MESH:D003920), insulin resistance (MESH:D007333), NASH (MESH:D065626), Metabolic syndrome (MESH:D024821), depression (MESH:D003866), COVID-19 (MESH:D000086382), NODAT (MESH:C565715)
- **Chemicals:** creatinine (MESH:D003404), VA (-), lipid (MESH:D008055), vitamin D. (MESH:D014807), alcohol (MESH:D000438), triglyceride (MESH:D014280), Cholesterol (MESH:D002784), blood sugar (MESH:D001786), steroids (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** R24W

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12795668/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12795668/full.md

## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12795668/full.md

---
Source: https://tomesphere.com/paper/PMC12795668