# Newly Developed Sarcopenia as a Prognostic Factor for Survival in Patients who Underwent Liver Transplantation

**Authors:** Ja Young Jeon, Hee-Jung Wang, So Young Ock, Weiguang Xu, Jung-Dong Lee, Jei Hee Lee, Hae Jin Kim, Dae Jung Kim, Kwan Woo Lee, Seung Jin Han

PMC · DOI: 10.1371/journal.pone.0143966 · PLoS ONE · 2015-11-30

## TL;DR

Newly developed sarcopenia after liver transplantation is linked to higher mortality risk, offering a new way to assess patient survival.

## Contribution

Identifies newly developed sarcopenia as a novel prognostic factor for post-LT survival.

## Key findings

- 14% of patients developed sarcopenia within one year after liver transplantation.
- Newly developed sarcopenia was an independent predictor of increased post-LT mortality.
- Sarcopenia in pre-LT patients did not improve after the transplant.

## Abstract

The relationship between a perioperative change in sarcopenic status and clinical outcome of liver transplantation (LT) is unknown. We investigated whether post-LT sarcopenia and changes in sarcopenic status were associated with the survival of patients.

This retrospective study was based on a cohort of 145 patients from a single transplant center who during a mean of 1 year after LT underwent computed tomography imaging evaluation. The cross-sectional area of the psoas muscle of LT patients was compared with that of age- and sex-matched healthy individuals. The Cox proportional hazards regression model was used to determine whether post-LT sarcopenia and changes in sarcopenic status affect post-LT survival.

The mean age at LT of the 116 male and 29 female patients was 50.2 ± 7.9 years; the mean follow-up duration was 51.6 ± 32.9 months. All pre-LT patients with sarcopenia still had sarcopenia 1 year after LT; 14 (15%) patients had newly developed sarcopenia. The mean survival duration was 91.8 ± 4.2 months for non-sarcopenic patients and 80.0 ± 5.2 months for sarcopenic patients (log-rank test, p = 0.069). In subgroup analysis, newly developed sarcopenia was an independent negative predictor for post-LT survival (hazard ratio: 10.53, 95% confidence interval: 1.37–80.93, p = 0.024).

Sarcopenia in LT recipients did not improve in any of the previously sarcopenic patients and newly developed within 1 year in others. Newly developed sarcopenia was associated with increased mortality. Newly developed sarcopenia can be used to stratify patients with regard to the risk of post-LT mortality.

## Full-text entities

- **Genes:** CABIN1 (calcineurin binding protein 1) [NCBI Gene 23523] {aka CAIN, KB-318B8.7, PPP3IN}
- **Diseases:** hepatic encephalopathy (MESH:D006501), infections (MESH:D007239), dyslipidemia (MESH:D050171), ascites (MESH:D001201), Sarcopenia (MESH:D055948), hepatomegaly (MESH:D006529), LT (MESH:D017093), People (MESH:C000719191), colon cancer (MESH:D015179), renal failure (MESH:D051437), end-stage liver disease (MESH:D058625), gastric cancer (MESH:D013274), loss of muscle mass (MESH:C536030), Death (MESH:D003643), acute myeloid leukemia (MESH:D015470), hypertension (MESH:D006973), HCC (MESH:D006528), ESRD (MESH:D007676), DM (MESH:D003920), fatty (MESH:D008067), hepatitis B virus cirrhosis (MESH:D006509), hypermetabolism (MESH:C565498), cirrhosis (MESH:D005355), biliary complications (MESH:D008107), acute liver failure (MESH:D017114), Cancer (MESH:D009369), bloodstream infection (MESH:D018805)
- **Chemicals:** CSA (MESH:D016572), methylprednisolone (MESH:D008775), Creatinine (MESH:D003404), MMF (MESH:D009173), lipid (MESH:D008055), Basiliximab (MESH:D000077552), glucose (MESH:D005947), Tacrolimus (MESH:D016559), mycopenolate mofetil (-), insulin (MESH:D007328), Steroid (MESH:D013256), carbohydrate (MESH:D002241)
- **Species:** Hepatitis B virus (no rank) [taxon 10407], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC4664264/full.md

## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC4664264/full.md

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Source: https://tomesphere.com/paper/PMC4664264