Sequential SAFE Score and Transient Elastography for Detecting Significant Fibrosis in Asian Patients with MASLD

Metabolic dysfunction–associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD),1 represents a global public health issue. Fibrosis stage is the most important risk for long-term undesirable outcomes.2,3 From recent meta-analyses, all-cause and liver-rela...

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Veröffentlicht in:Clinical gastroenterology and hepatology 2024-12, Vol.22 (12), p.2535-2537
Hauptverfasser: Kaewdech, Apichat, Sripongpun, Pimsiri, Treeprasertsuk, Sombat, Charatcharoenwitthaya, Phunchai, Chan, Wah Kheong, Chamroonkul, Naichaya, Ng, Cheng Han, Muthiah, Mark Dhinesh, Dan, Yock Young, Kim, W. Ray
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Sprache:eng
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Zusammenfassung:Metabolic dysfunction–associated steatotic liver disease (MASLD), formerly known as nonalcoholic fatty liver disease (NAFLD),1 represents a global public health issue. Fibrosis stage is the most important risk for long-term undesirable outcomes.2,3 From recent meta-analyses, all-cause and liver-related mortalities significantly increased from fibrosis stage 2 (significant fibrosis; F≥2) onward.4,5 In primary care setting, those with F≥2 should be referred to hepatologists; therefore, noninvasive tests to stratify risk of patients with MASLD are crucial. Steatosis-associated fibrosis estimator (SAFE) was recently developed to predict F≥2.6 SAFE has been externally validated and outperformed fibrosis-4 (FIB-4) and NAFLD fibrosis score (NFS).7,8 Recently, international guidelines proposed sequential diagnostic steps, initially using FIB-4 and then transient elastography (TE) in non-low-risk patients.9,10 However, the guidelines focused on identifying advanced fibrosis (F≥3), which might be too late. This study aimed to compare the performance among SAFE, FIB-4, and NFS, and evaluate SAFE-TE sequential approach. We hypothesized that by initially using SAFE, the proportion of patients misclassified as low risk despite already having F≥2 could be diminished.
ISSN:1542-3565
1542-7714
1542-7714
DOI:10.1016/j.cgh.2024.06.003