Revisiting the steatosis‐associated fibrosis estimator score in young Asian subjects with steatotic liver disease and consideration for population variability

Author:

Yang Jiwon1,Choi Won‐Mook1ORCID,Lee Danbi1,Shim Ju Hyun1,Kim Kang Mo1ORCID,Lim Young‐Suk1ORCID,Lee Han Chu1ORCID,Choi Jonggi1ORCID

Affiliation:

1. Department of Gastroenterology Liver Center, Asan Medical Center, University of Ulsan College of Medicine Seoul Republic of Korea

Abstract

AbstractBackground and AimThe steatosis‐associated fibrosis estimator (SAFE) score has been developed to distinguish clinically significant fibrosis in patients with steatotic liver disease (SLD). However, validation of its performance in Asian subjects is limited. This study aimed to evaluate the performance of the SAFE score in Asian subjects with biopsy‐proven SLD and in different subgroups according to age, sex, and body mass index.MethodsWe retrospectively analyzed 6383 living liver donors who underwent a liver biopsy between 2005 and 2023. Of these, 1551 subjects with biopsy‐proven SLD were included. The performance of the SAFE score was evaluated using areas under the curve and compared with those of the nonalcoholic fatty liver disease fibrosis score (NFS) and fibrosis‐4 index (FIB‐4).ResultsThe prevalence of clinically significant fibrosis in the cohort was 2.2%. The proportion of subjects with a “low‐risk” SAFE score was the highest (91.0%), followed by those with “intermediate‐risk” (7.8%) and “high‐risk” (1.2%) scores. The prevalence of fibrosis in subjects with low‐risk, intermediate‐risk, and high‐risk scores was 1.6%, 6.6%, and 21.1%, respectively. The SAFE outperformed FIB‐4 and NFS (area under the curve: 0.70 vs 0.64 for both NFS and FIB‐4). However, it showed low diagnostic accuracy and sensitivity (27%) at the low cutoff (SAFE < 0) in subjects aged 30–39 years (fibrosis: 1.2%), despite having a high negative predictive value (0.99).ConclusionWhile the SAFE score demonstrates superior performance compared with other noninvasive tests in Asian subjects with SLD, its performance varies across age groups. In younger subjects, particularly, its performance may be more limited.

Funder

National Research Foundation of Korea

Gilead Research Scholars

Publisher

Wiley

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