# Serum fibroblast growth factor 21 is a novel biomarker of cachexia in chronic liver disease

**Authors:** Takatsugu Tanaka, Goki Suda, Masatsugu Ohara, Osamu Maehara, Tomoka Yoda, Qingjie Fu, Zijian Yang, Naohiro Yasuura, Akimitsu Meno, Takashi Sasaki, Risako Kohya, Takashi Kitagataya, Naoki Kawagishi, Masato Nakai, Takuya Sho, Shunsuke Ohnishi, Naoya Sakamoto

PMC · DOI: 10.3389/fnut.2026.1730695 · Frontiers in Nutrition · 2026-02-18

## TL;DR

Serum FGF21 is a new biomarker for identifying cachexia in chronic liver disease patients, which could help improve early detection and treatment.

## Contribution

FGF21 is identified as a novel and independent serum biomarker for cachexia in chronic liver disease.

## Key findings

- Patients with cachexia had significantly higher serum FGF21 levels compared to those without.
- FGF21 was the only biomarker independently associated with cachexia in multivariable analysis.
- Cachexia independently predicted worse overall survival in CLD patients.

## Abstract

Cachexia is associated with poor prognosis in chronic liver disease (CLD), yet robust predictors remain poorly defined. This study examined clinical factors and serum biomarkers associated with cachexia in patients with CLD.

We analyzed 356 of 526 patients with CLD who had complete cachexia assessment and available stored serum samples. In a discovery cohort (n = 240; Aug 2014–Jun 2023), serum fibroblast growth factor 21 (FGF21), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) were measured. Multivariable logistic regression and receiver operating characteristic analyses were used to identify independent predictors and optimal cutoff values. Findings were subsequently evaluated in an independent validation cohort (n = 116; Jul 2023–May 2025).

Median age was 68 years (range 19–90), 65.8% of participants were male, and 24.6% had cachexia, which independently predicted worse overall survival (hazard ratio 1.64; 95% CI 1.03–2.62; p = 0.038). Patients with cachexia had higher serum FGF21 concentrations than those without cachexia (median, 292 vs. 177 pg./mL; p = 0.002), whereas IL-6 and TNF-α levels did not differ significantly between groups. FGF21 was the only biomarker independently associated with cachexia (odds ratio, 1.71; 95% CI, 1.10–2.66; p = 0.016). Advanced Child–Pugh class and platelet count were identified as additional independent clinical predictors.

Serum FGF21 independently predicts cachexia in CLD and may facilitate earlier identification of at-risk patients, enabling timely intervention to improve clinical outcomes.

## Linked entities

- **Proteins:** IL6 (interleukin 6)

## Full-text entities

- **Genes:** SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, FGF21 (fibroblast growth factor 21) [NCBI Gene 26291], ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, FAP (fibroblast activation protein alpha) [NCBI Gene 2191] {aka DPPIV, FAPA, FAPalpha, SIMP}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, KLB (klotho beta) [NCBI Gene 152831] {aka BKL}
- **Diseases:** death (MESH:D003643), undernutrition (MESH:D044342), decreased muscle strength (MESH:D009123), hepatic deterioration (MESH:D017114), weight loss (MESH:D015431), appetite loss (MESH:D001068), heart failure (MESH:D006333), chronic illnesses (MESH:D002908), HCC (MESH:D006528), metabolic disturbances (MESH:D024821), CLD (MESH:D008107), inflammation (MESH:D007249), muscle atrophy (MESH:D009133), anorexia (MESH:D000855), chronic kidney disease (MESH:D051436), LC (MESH:D008103), diabetes mellitus (MESH:D003920), muscle weakness (MESH:D018908), starvation (MESH:D013217), cancer (MESH:D009369), reduced handgrip strength (MESH:D001523), chronic obstructive pulmonary disease (MESH:D029424), Cachexia (MESH:D002100), metabolic dysfunction-associated steatohepatitis (MESH:D005234), metabolic (MESH:D008659)
- **Chemicals:** carbohydrate (MESH:D002241), BCAA (MESH:D000597)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12956663/full.md

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Source: https://tomesphere.com/paper/PMC12956663