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. 2025 Aug 7.
doi: 10.1055/a-2592-1431. Online ahead of print.

UDFF and Auto pSWE accurately assess liver steatosis and fibrosis risk in obese patients with MASLD

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Free article

UDFF and Auto pSWE accurately assess liver steatosis and fibrosis risk in obese patients with MASLD

Nina Dominik et al. Ultraschall Med. .
Free article

Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) can progress to fibrosis and cirrhosis. Fibrosis and steatosis assessment with vibration-controlled transient elastography (VCTE) and controlled attenuation parameter (CAP) requires a dedicated device and time to obtain ≥10 reliable measurements. Auto pSWE allows for the simultaneous collection of 15 ARFI-based liver stiffness measurements (LSM) and UDFF-based steatosis assessment in a single acquisition.This prospective study included patients undergoing liver biopsy, primarily during bariatric surgery, between 11/2021-12/2023. Paired LSM by Auto pSWE/VCTE and steatosis assessments by UDFF/CAP were performed within a median of 1 day before or after biopsy.134 patients (65% women, mean age: 42.6±13.3 years) with a high prevalence of obesity (mean BMI: 42.7±10.4; MASLD etiology: 88%) were included. Liver biopsy showed significant fibrosis (≥F2) in 27% of patients and moderate steatosis (≥S2) in 51%. A single 1×15 Auto pSWE acquisition and one UDFF measurement were as accurate as the median of 5 measurements. Auto pSWE (AUC: ≥F2=0.58, ≥F3=0.96, F4=0.97) and VCTE (AUC: ≥F2=0.60, ≥F3=0.92, F4=0.93) demonstrated high accuracy for advanced fibrosis stages. UDFF (AUC: ≥S1=0.79, ≥S2=0.78, S3=0.67) and CAP showed similar diagnostic accuracy.Auto pSWE and UDFF provide accurate, noninvasive tests for advanced liver fibrosis and steatosis in MASLD, even in severely obese patients. Notably, Auto pSWE captures 15 LSM with UDFF in a single acquisition, saving time and eliminating the need for a dedicated device.

Die mit Stoffwechselstörungen assoziierte steatotische Lebererkrankung (Metabolic dysfunction-associated steatotic liver disease; MASLD) kann zu Fibrose und Zirrhose führen. Die nicht-invasive Beurteilung von Fibrose und Steatose mittels vibrationskontrollierter transienter Elastografie (VCTE) und Controlled-Attenuation-Parameter-(CAP-)Technologie erfordert ein spezielles Gerät und mindestens 10 verlässliche Messungen. Die ultraschall-basierte Fettfraktion (UDFF) und die Auto-Punkt-Scherwelle (Auto-pSWE) ermöglichen eine Quantifizierung von Lebersteatose und -fibrose in nur einer Akquisition.Diese prospektive Studie umfasste Patient:innen, die zwischen 11/2021 und 12/2023 eine Leberbiopsie erhielten. Paarweise Lebersteifigkeits- und Steatosemessungen durch Auto pSWE/UDFF und VCTE/CAP wurden einen Tag vor oder nach der Leberbiopsie durchgeführt.134 Patient:innen mit hoher Adipositas-Prävalenz wurden eingeschlossen. Eine einzige Akquisition (welche 15 pSWE-Messungen erfasst) durch Auto-pSWE lieferte dieselbe diagnostische Genauigkeit wie der Median aus 5 Messungen. Auto-pSWE (≥F2, AUC=0,58; ≥F3, AUC=0,96; F4, AUC=0,97) und VCTE zeigten eine hohe diagnostische Genauigkeit für die Erfassung einer fortgeschrittenen Fibrose. Die Diagnosegenauigkeit von UDFF (≥S1, AUC=0,79; ≥S2, AUC=0,78) war vergleichbar mit CAP.Auto pSWE und UDFF sind präzise, nicht-invasive Methoden zur Diagnostik fortgeschrittener Leberfibrose und -steatose bei Patient:innen mit MASLD. Die simultane Erfassung von 15 pSWE-Messungen und UDFF in einer Akquisition ist zeitsparend und erfordert kein spezielles Gerät.

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Conflict of interest statement

The following authors declared no conflicts: N.D., L.N., M.S., B.H., Lu.H., Lo.H., L.F., J.J., L.G., F.B.L., and G.P. M.J. has served as a speaker and consultant for Gilead Sciences and has received travel support from the same company. G.S. received travel support from Gilead. B.Si. received travel support from both AbbVie and Gilead. L.B. received speaker fees from Chiesi and Gilead. M.T. received speaker fees from BMS, Falk Foundation, Gilead, Intercept, Janssen, Madrigal, MSD, and Roche. He has also served as an advisor for AbbVie, Albireo, BiomX, Boehringer Ingelheim, Cymabay, Falk Pharma GmbH, Genfit, Gilead, Hightide, Intercept, Janssen, MSD, Novartis, Phenex, Pliant, Rectify, Regulus, Siemens, and Shire. In addition, he received travel support from AbbVie, Falk, Gilead, Intercept, and Janssen, and research grants from Albireo, Alnylam, Cymabay, Falk, Gilead, Intercept, MSD, Takeda, and UltraGenyx. He is also a co-inventor on patents concerning the medical use of norUDCA, filed by the Medical Universities of Graz and Vienna. B.M. received a speaker fee from Astellas Pharma. M.M. served as a speaker, consultant, and/or advisory board member for AbbVie, Collective Acumen, Gilead, Takeda, and W. L. Gore & Associates, and received travel support from AbbVie and Gilead. T.R. received grant support from AbbVie, Boehringer Ingelheim, Gilead, Gore, Intercept, MSD, Myr Pharmaceuticals, Philips Healthcare, Pliant, and Siemens; speaker honoraria from AbbVie, Gilead, Gore, Intercept, Roche, and MSD; consulting/advisory board fees from AbbVie, Bayer, Boehringer Ingelheim, Gilead, Intercept, MSD, and Siemens; and travel support from AbbVie, Boehringer Ingelheim, Gilead, and Roche. D.B. received grant support from Gilead, travel support from Siemens, AbbVie, and Gilead, and speaker honoraria from AbbVie and Siemens.

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