TY - JOUR
T1 - MetALD
T2 - Diagnosis and Prognosis With Non-Invasive Tests
AU - Torp, Nikolaj
AU - Israelsen, Mads
AU - Johansen, Stine
AU - Semmler, Georg
AU - Dalby Hansen, Camilla
AU - Bech, Katrine Tholstrup
AU - Andersen, Mette Lehmann
AU - Thorhauge, Katrine Holtz
AU - Andersen, Peter
AU - Schnefeld, Helle Lindholm
AU - Hansen, Johanne Kragh
AU - Jensen, Ellen Lyngbeck
AU - Hansen, Emil Deleuran
AU - Villesen, Ida
AU - Lindvig, Katrine Prier
AU - Leeming, Diana Julie
AU - Karsdal, Morten
AU - Tsochatzis, Emmanuel A.
AU - Thiele, Maja
AU - Krag, Aleksander
N1 - Publisher Copyright:
© 2025 The Author(s). Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd.
PY - 2025/11
Y1 - 2025/11
N2 - Background: Non-invasive tests (NITs) are central to diagnosing and stratifying risk in steatotic liver disease (SLD). However, it remains unclear whether guideline-recommended NIT cut-offs apply to metabolic and alcohol-related liver disease (MetALD). Aim: Evaluate the diagnostic and prognostic performance of five NITs in patients with MetALD. Methods: Single-centre study with 423 SLD patients, of whom 102 (24%) had MetALD. Patients were classified using histological or controlled attenuation parameter-defined hepatic steatosis and self-reported alcohol intake. We assessed the circulating markers of FIB-4, LiverRisk score, ELF and ADAPT together with transient elastography (TE) using established cut-offs for advanced fibrosis (≥ F3). Liver histology served as reference. Prognostic performance for hepatic decompensation and all-cause mortality was evaluated over a median follow-up of 62 months. Results: Among circulating NITs in MetALD, ELF and ADAPT both had the highest diagnostic accuracy (AUROC = 0.90), while it was lowest with LiverRisk score (AUROC = 0.74). The indeterminate zone between rule-out and rule-in cut-offs was largest for FIB-4 (34%). TE and circulating NIT concordance was highest for LiverRisk score (81%) to rule-out ≥ F3, and highest for ELF (88%) to rule-in ≥ F3. All included NITs predicted decompensation-free survival with their corresponding rule-out or rule-in cut-offs. A sequential 2-tier testing strategy (FIB-4 → TE) effectively stratified risk of decompensation. Incorporating a second-tier test (ELF or ADAPT) before TE reduced the number of TE referrals by 43% and 45%, without loss of prognostic performance. Conclusion: Widely available NITs are applicable for MetALD, where cut-offs can be used to diagnose advanced fibrosis and predict clinical outcomes.
AB - Background: Non-invasive tests (NITs) are central to diagnosing and stratifying risk in steatotic liver disease (SLD). However, it remains unclear whether guideline-recommended NIT cut-offs apply to metabolic and alcohol-related liver disease (MetALD). Aim: Evaluate the diagnostic and prognostic performance of five NITs in patients with MetALD. Methods: Single-centre study with 423 SLD patients, of whom 102 (24%) had MetALD. Patients were classified using histological or controlled attenuation parameter-defined hepatic steatosis and self-reported alcohol intake. We assessed the circulating markers of FIB-4, LiverRisk score, ELF and ADAPT together with transient elastography (TE) using established cut-offs for advanced fibrosis (≥ F3). Liver histology served as reference. Prognostic performance for hepatic decompensation and all-cause mortality was evaluated over a median follow-up of 62 months. Results: Among circulating NITs in MetALD, ELF and ADAPT both had the highest diagnostic accuracy (AUROC = 0.90), while it was lowest with LiverRisk score (AUROC = 0.74). The indeterminate zone between rule-out and rule-in cut-offs was largest for FIB-4 (34%). TE and circulating NIT concordance was highest for LiverRisk score (81%) to rule-out ≥ F3, and highest for ELF (88%) to rule-in ≥ F3. All included NITs predicted decompensation-free survival with their corresponding rule-out or rule-in cut-offs. A sequential 2-tier testing strategy (FIB-4 → TE) effectively stratified risk of decompensation. Incorporating a second-tier test (ELF or ADAPT) before TE reduced the number of TE referrals by 43% and 45%, without loss of prognostic performance. Conclusion: Widely available NITs are applicable for MetALD, where cut-offs can be used to diagnose advanced fibrosis and predict clinical outcomes.
KW - hepatic fibrosis
KW - liver disease management
KW - prognostic biomarkers
KW - referral pathways
KW - risk stratification
UR - https://www.scopus.com/pages/publications/105012876174
U2 - 10.1111/apt.70281
DO - 10.1111/apt.70281
M3 - Journal article
C2 - 40785346
AN - SCOPUS:105012876174
SN - 0269-2813
VL - 62
SP - 990
EP - 1002
JO - Alimentary Pharmacology and Therapeutics
JF - Alimentary Pharmacology and Therapeutics
IS - 10
ER -