Prospective direct comparison of non‐invasive liver tests in outpatients with type 2 diabetes using intention‐to‐diagnose analysis

Author:

Poynard Thierry12ORCID,Deckmyn Olivier2,Peta Valentina2,Paradis Valérie3,Gautier Jean‐Francois4,Brzustowski Angélique5,Bedossa Pierre3,Castera Laurent5,Pol Stanislas6ORCID,Valla Dominique5,

Affiliation:

1. Centre de Recherche Saint‐Antoine (CRSA) INSERM, Institute of Cardiometabolism and Nutrition (ICAN), Sorbonne Université Paris France

2. BioPredictive Paris France

3. Department of Pathology AP‐HP, Beaujon Hospital Clichy France

4. Department of Diabetes and Endocrinology APHP, INSERM U1138, Hôpital Lariboisière Paris France

5. Department of Hepatology AP‐HP, Beaujon Hospital Clichy France

6. Department of Hepatology Cochin Hospital, Université Paris Descartes Paris France

Abstract

SummaryBackgroundNo prospective diagnostic studies have directly compared widespread non‐invasive liver tests in patients with type 2 diabetes (T2D) using the intention‐to‐diagnose method for each of the three main histological features of metabolic dysfunction associated steatotic liver disease ‐ namely fibrosis, metabolic dysfunction‐associated steatohepatitis (MASH), and steatosis.AimsTo compare the performance of nine tests using the intention‐to‐diagnose rather than the standard method, which would exclude non‐evaluable participantsMethodsBiopsy was used as the reference with predetermined cut‐offs, advanced fibrosis being the main endpoint. The Nash‐FibroTest panel including FibroTest‐T2D, SteatoTest‐T2D and MashTest‐T2D was optimised for type 2 diabetes. FibroTest‐T2D was compared to vibration‐controlled transient elastography stiffness (VCTE), two‐dimensional shear‐wave elastography stiffness (TD‐SWE), and Fibrosis‐4 blood test. NashTest‐T2D was compared to aspartate aminotransferase. SteatoTest‐T2D was compared to the controlled attenuation parameter and the hepatorenal gradient.ResultsAmong 402 cases, non‐evaluable tests were 6.7% for VCTE, 4.0% for hepatorenal gradient, 3.2% for controlled attenuation parameter, 1.5% for TD‐SWE, 1.2% for NashTest‐T2D, and 0.02% for Fibrosis‐4, aspartate aminotransferase and SteatoTest‐T2D. The VCTE AUROC for advanced fibrosis was over‐estimated by 6% (0.83 [95% CI: 0.78–0.87]) by standard analysis compared to intention‐to‐diagnose (0.77 [0.72–0.81] p = 0.008). The AUROCs for advanced fibrosis did not differ significantly in intention‐to‐diagnose between FibroTest‐T2D (0.77; 95% CI: 0.73–0.82), VCTE (0.77; 95% CI: 0.72–0.81) and TD‐SWE(0.78; 0.74–0.83) but were all higher than the Fibrosis‐4 score (0.70; 95% CI all differences ≥7%; p ≤ 0.03). For MASH, MashTest‐T2D had a higher AUROC (0.76; 95% CI: 0.70–0.80) than aspartate aminotransferase (0.72; 95% CI: 0.66–0.77; p = 0.035). For steatosis, AUROCs did not differ significantly between SteatoTest‐T2D, controlled attenuation parameter and hepatorenal gradient.ConclusionsIn intention‐to‐diagnose analysis, FibroTest‐T2D, TD‐SWE and VCTE performed similarly for staging fibrosis, and out‐performed Fibrosis‐4 in outpatients with type 2 diabetes. The standard analysis over‐estimated VCTE performance.ClinicalTrial.gov: NCT03634098.

Funder

Université Paris Descartes

Centre National de la Recherche Scientifique

Publisher

Wiley

Subject

Pharmacology (medical),Gastroenterology,Hepatology

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