TY - JOUR
T1 - Global patterns of utilization of noninvasive tests for the clinical management of metabolic dysfunction–associated steatotic liver disease
AU - Allen, Alina M.
AU - Lazarus, Jeffrey V.
AU - Alkhouri, Naim
AU - Noureddin, Mazen
AU - Wong, Vincent Wai Sun
AU - Tsochatzis, Emmanuel A.
AU - de Avila, Leyla
AU - Racila, Andrei
AU - Nader, Fatema
AU - Mark, Henry E.
AU - Henry, Linda
AU - Stepanova, Maria
AU - Castera, Laurent
AU - Younossi, Zobair M.
N1 - Publisher Copyright:
Copyright © 2025 The Author(s).
PY - 2025/4/30
Y1 - 2025/4/30
N2 - Background: Noninvasive tests (NITs) are used to risk-stratify metabolic dysfunction–associated steatotic liver disease. The aim was to survey global patterns of real-world use of NITs. Methods: A 38-item survey was designed by the Global NASH Council. Providers were asked about risks for advanced fibrosis, which NITs (cutoff values) they use to risk-stratify liver disease, monitor progression, and which professional guidelines they follow. Results: A total of 321 participants from 43 countries completed the survey (54% hepatologists, 28% gastroenterologists, and 18% other). Of the respondents, 85% would risk-stratify patients with type 2 diabetes, obesity (82%), or abnormal liver enzymes (73%). Among NITs to rule out significant or advanced fibrosis, transient elastography (TE) and fibrosis-4 (FIB-4) were most used, followed by NAFLD Fibrosis Score, Enhanced Liver Fibrosis, and magnetic resonance elastography. The cutoffs for ruling out significant fibrosis varied considerably between practices and from guidelines, with only 50% using TE < 8 kPa, 65% using FIB-4 < 1.30 for age < 65, and 41% using FIB-4 < 2.00 for age ≥ 65. Similar variability was found for ruling in advanced fibrosis, where thresholds of FIB-4 ≥ 2.67 and TE ≥ 10 kPa were used by 20% and 17%, respectively. To establish advanced fibrosis, 48% would use 2 NITs while 23% would consider 1 NIT, and 17% would confirm with liver biopsy. TE was used by > 75% to monitor, and 66% would monitor (intermediate or high risk) annually. Finally, 65% follow professional guideline recommendations regarding NITs. Conclusions: In clinical practice, there is variability in NIT use and their thresholds. Additionally, there is suboptimal adherence to professional societies’ guidelines.
AB - Background: Noninvasive tests (NITs) are used to risk-stratify metabolic dysfunction–associated steatotic liver disease. The aim was to survey global patterns of real-world use of NITs. Methods: A 38-item survey was designed by the Global NASH Council. Providers were asked about risks for advanced fibrosis, which NITs (cutoff values) they use to risk-stratify liver disease, monitor progression, and which professional guidelines they follow. Results: A total of 321 participants from 43 countries completed the survey (54% hepatologists, 28% gastroenterologists, and 18% other). Of the respondents, 85% would risk-stratify patients with type 2 diabetes, obesity (82%), or abnormal liver enzymes (73%). Among NITs to rule out significant or advanced fibrosis, transient elastography (TE) and fibrosis-4 (FIB-4) were most used, followed by NAFLD Fibrosis Score, Enhanced Liver Fibrosis, and magnetic resonance elastography. The cutoffs for ruling out significant fibrosis varied considerably between practices and from guidelines, with only 50% using TE < 8 kPa, 65% using FIB-4 < 1.30 for age < 65, and 41% using FIB-4 < 2.00 for age ≥ 65. Similar variability was found for ruling in advanced fibrosis, where thresholds of FIB-4 ≥ 2.67 and TE ≥ 10 kPa were used by 20% and 17%, respectively. To establish advanced fibrosis, 48% would use 2 NITs while 23% would consider 1 NIT, and 17% would confirm with liver biopsy. TE was used by > 75% to monitor, and 66% would monitor (intermediate or high risk) annually. Finally, 65% follow professional guideline recommendations regarding NITs. Conclusions: In clinical practice, there is variability in NIT use and their thresholds. Additionally, there is suboptimal adherence to professional societies’ guidelines.
KW - 2D-SWE
KW - ELF
KW - Fib-4
KW - risk stratification
KW - VCTE
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U2 - 10.1097/HC9.0000000000000678
DO - 10.1097/HC9.0000000000000678
M3 - Article
C2 - 40304566
AN - SCOPUS:105005178178
SN - 2471-254X
VL - 9
JO - Hepatology Communications
JF - Hepatology Communications
IS - 5
M1 - e0678
ER -