Serum growth differentiation factor 15 is a novel biomarker with high predictive capability for liver cancer occurrence in patients with MASLD regardless of liver fibrosis

Author:

Kumazaki Shusuke1,Hikita Hayato1,Tahata Yuki1,Sung Ji Hyun1,Fukumoto Kenji1,Myojin Yuta1,Sakane Sadatsugu1,Murai Kazuhiro1,Sasaki Yoichi1,Shirai Kumiko1,Saito Yoshinobu1,Kodama Takahiro1,Kakita Naruyasu2,Takahashi Hirokazu3,Toyoda Hidenori4ORCID,Suda Goki5ORCID,Morii Eiichi6,Kojima Takashi7,Ebihara Takeshi7,Shimizu Kentaro7,Sasaki Yutaka8,Tatsumi Tomohide1,Takehara Tetsuo1ORCID

Affiliation:

1. Department of Gastroenterology and Hepatology Osaka University Graduate School of Medicine Osaka Japan

2. Department of Gastroenterology and Hepatology Kaizuka City Hospital Osaka Japan

3. Liver Center, Saga University Hospital, Faculty of Medicine Saga University Saga Japan

4. Department of Gastroenterology and Hepatology Ogaki Municipal Hospital Ogaki Japan

5. Department of Gastroenterology and Hepatology, Graduate School of Medicine Hokkaido University Sapporo Japan

6. Department of Pathology Osaka University Graduate School of Medicine Osaka Japan

7. Department of Traumatology and Acute Critical Medicine Osaka University Graduate School of Medicine Osaka Japan

8. Department of Gastroenterology Osaka Central Hospital Osaka Japan

Abstract

SummaryBackground and AimsAlthough metabolic dysfunction‐associated steatotic liver disease (MASLD) patients with a Fib‐4 index >1.3 are recommended for fibrosis evaluation via elastography or biopsy, a more convenient method identifying high‐risk populations requiring follow‐up is needed. We explored the utility of serum levels of growth differentiation factor‐15 (GDF15), a cell stress‐responsive cytokine related to metabolic syndrome, for stratifying the risk of clinical events in MASLD patients.MethodsSerum GDF15 levels were measured in 518 biopsy‐performed MASLD patients, 216 MASLD patients for validation, and 361 health checkup recipients with MASLD.ResultsIn the biopsy‐MASLD cohort, multivariate analysis indicated that the serum GDF15 level was a risk factor for liver cancer, independent of the fibrosis stage or Fib‐4 index. Using a GDF15 cutoff of 1.75 ng/mL based on the Youden index, high‐GDF15 patients, regardless of fibrosis status, had a higher liver cancer incidence rate. While patients with a Fib‐4 index <1.3 or low‐GDF15 rarely developed liver cancer, high‐GDF15 patients with a Fib‐4 index >1.3 developed liver cancer and decompensated liver events at significantly higher rates and had poorer prognoses. In the validation cohort, high‐GDF15 patients had significantly higher incidences of liver cancer and decompensated liver events and poorer prognoses than low‐GDF15 patients, whether limited to high‐Fib‐4 patients. Among health checkup recipients with MASLD, 23.0% had a Fib‐4 index >1.3, 2.7% had a Fib‐4 index >1.3 and >1.75 ng/mL GDF15.ConclusionsSerum GDF15 is a biomarker for liver cancer with high predictive capability and is useful for identifying MASLD patients requiring regular surveillance.

Funder

Japan Agency for Medical Research and Development

Japan Society for the Promotion of Science

Publisher

Wiley

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