Affiliation:
1. Medical Data Analytics Center, Department of Medicine and Therapeutics The Chinese University of Hong Kong Hong Kong
2. State Key Laboratory of Digestive Disease, Institute of Digestive Disease The Chinese University of Hong Kong Hong Kong
3. Division of Gastroenterology and Hepatology, Department of Medicine Stanford University Redwood City California USA
4. Gastroenterology and Hepatology Unit, Division of Internal Medicine Prince of Songkla University Hat Yai Thailand
Abstract
AbstractBackground & AimsThe steatosis‐associated fibrosis estimator (SAFE) score was developed to detect clinically significant liver fibrosis in patients with NAFLD in the United States. We compare the performance of the SAFE score and other non‐invasive tests to diagnose liver fibrosis and to correlate the scores with liver‐related outcomes in patients with NAFLD in Hong Kong.MethodsThis was a retrospective cohort study involving two data sets. The first cohort was a biopsy cohort of NAFLD patients (n = 279), and the second was a territory‐wide cohort of NAFLD patients (n = 4603) retrieved from a territory‐wide electronic healthcare database in Hong Kong.ResultsIn detecting significant fibrosis, liver stiffness measured by transient elastography had the highest area under the receiver operating characteristic curve (AUROC) (.844), followed by SAFE score (.773). SAFE score had the highest AUROC among blood‐based algorithms (.773 vs. .746 for FIB‐4, .697 for APRI). Based on cut‐off values of SAFE score (0 and 100 points), 854 (18.6%), 1596 (34.6%) and 2153 (46.8%) were in the low‐, intermediate‐ and high‐risk groups, respectively, in the territory‐wide cohort. Six (.7%), 15 (.9%) and 59 (2.7%) developed liver‐related events in those three groups respectively. Among patients who had liver‐related events at 5 years, using the high cut‐off, SAFE score could predict 84.9% of patients accurately, compared to 40.9% for FIB‐4 and 27.2% for APRI.ConclusionThe SAFE score performed well and better than other blood‐based markers in diagnosing significant fibrosis and predicting liver‐related events in Asian patients with NAFLD.
Funder
Chinese University of Hong Kong
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