Noninvasive assessment of liver disease severity in patients with nonalcoholic fatty liver disease (NAFLD) and type 2 diabetes

Author:

Pennisi Grazia1ORCID,Enea Marco1ORCID,Falco Vincenzo2ORCID,Aithal Guruprasad P.34ORCID,Palaniyappan Naaventhan34ORCID,Yilmaz Yusuf5ORCID,Boursier Jerome67ORCID,Cassinotto Christophe8ORCID,de Lédinghen Victor9ORCID,Chan Wah Kheong10ORCID,Mahadeva Sanjiv10ORCID,Eddowes Peter34ORCID,Newsome Philip34ORCID,Karlas Thomas11ORCID,Wiegand Johannes11ORCID,Wong Vincent Wai-Sun12ORCID,Schattenberg Jörn M.1314ORCID,Labenz Christian1314ORCID,Kim Won15ORCID,Lee Myoung Seok15ORCID,Lupsor-Platon Monica16ORCID,Cobbold Jeremy F. L.17ORCID,Fan Jian-Gao18ORCID,Shen Feng18ORCID,Staufer Katharina1920ORCID,Trauner Michael19ORCID,Stauber Rudolf21ORCID,Nakajima Atsushi22ORCID,Yoneda Masato22ORCID,Bugianesi Elisabetta23ORCID,Younes Ramy23ORCID,Gaia Silvia23ORCID,Zheng Ming-Hua2425ORCID,Cammà Calogero12ORCID,Anstee Quentin M.2627ORCID,Mózes Ferenc E.28ORCID,Pavlides Michael1728ORCID,Petta Salvatore12ORCID

Affiliation:

1. Sezione di Gastroenterologia, PROMISE, University of Palermo, Italy

2. Department of Economics and Statistics, University of Palermo, Palermo, Italy

3. NIHR Nottingham Biomedical Research Centre (BRC), Nottingham University Hospitals NHS Trust and the University of Nottingham, Nottingham, UK

4. Nottingham Digestive Diseases Centre, Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK

5. Department of Gastroenterology, School of Medicine, Recep Tayyip Erdogan University, Rize, Turkey

6. Hepato-Gastroenterology Department, Angers University Hospital, Angers, France

7. HIFIH Laboratory, UPRES EA3859, Angers University, Angers, France

8. Department of Diagnostic and Interventional Radiology, Saint-Eloi Hospital, University Hospital of Montpellier, Montpellier, France

9. Hepatology Unit, University Hospital Bordeaux and INSERM U-1053, Bordeaux University, Pessac, France

10. Department of Medicine, Faculty of Medicine, University of Malaya, Malaysia

11. Department of Oncology, Gastroenterology, Hepatology, Pulmonology and Infectious Diseases, University Hospital Leipzig, Leipzig, Germany

12. Department of Medicine and Therapeutics, Faculty of Medicine, The Chinese University of Hong Kong

13. Department of Internal Medicine I, University Medical Center of the Johannes Gutenberg-University, Mainz, Germany

14. Cirrhosis Center Mainz (CCM), University Medical Center of the Johannes Gutenberg-University, Mainz, Germany

15. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul Metropolitan Government Boramae Medical Center, Seoul, Korea

16. Department of Medical Imaging, Iuliu Hatieganu, University of Medicine and Pharmacy, Regional Institute of Gastroenterology and Hepatology “Prof. Dr. Octavian Fodor”, Cluj-Napoca, Romania

17. Translational Gastroenterology Unit, University of Oxford, Oxford, UK

18. Department of Gastroenterology, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China

19. Division of Gastroenterology & Hepatology, Department of Internal Medicine III, Medical University of Vienna, Austria

20. Division of Transplantation, Department of General Surgery, Medical University of Vienna, Austria

21. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Medical University of Graz, Austria

22. Department of Gastroenterology and Hepatology, Yokohama City University School of Medicine, Yokohama, Japan

23. Division of Gastroenterology and Hepatology, Department of Medical Sciences, University of Turin, Italy

24. Department of Hepatology, MAFLD Research Center, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China

25. Key Laboratory of Diagnosis and Treatment for The Development of Chronic Liver Disease in Zhejiang Province, Wenzhou, China

26. Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, Tyne and Wear, UK

27. Newcastle NIHR Biomedical Research Center, Newcastle upon Tyne Hospitals NHS Trust, Newcastle upon Tyne, Tyne and Wear, UK

28. Radcliffe Department of Medical Sciences, Cardiovascular Medicine, University of Oxford, Oxford, UK

Abstract

Background and Aims: We evaluated the diagnostic accuracy of simple, noninvasive tests (NITs) in NAFLD patients with type 2 diabetes (T2D). Methods and Results: This was an individual patient data meta-analysis of 1780 patients with biopsy-proven NAFLD and T2D. The index tests of interest were FIB-4, NAFLD Fibrosis Score (NFS), aspartate aminotransferase-to-platelet ratio index, liver stiffness measurement (LSM) by vibration-controlled transient elastography, and AGILE 3+. The target conditions were advanced fibrosis, NASH, and fibrotic NASH(NASH plus F2-F4 fibrosis). The diagnostic performance of noninvasive tests. individually or in sequential combination, was assessed by area under the receiver operating characteristic curve and by decision curve analysis. Comparison with 2278 NAFLD patients without T2D was also made. In NAFLD with T2D LSM and AGILE 3+ outperformed, both NFS and FIB-4 for advanced fibrosis (area under the receiver operating characteristic curve:LSM 0.82, AGILE 3+ 0.82, NFS 0.72, FIB-4 0.75, aspartate aminotransferase-to-platelet ratio index 0.68; p < 0.001 of LSM-based versus simple serum tests), with an uncertainty area of 12%–20%. The combination of serum-based with LSM-based tests for advanced fibrosis led to a reduction of 40%–60% in necessary LSM tests. Decision curve analysis showed that all scores had a modest net benefit for ruling out advanced fibrosis at the risk threshold of 5%–10% of missing advanced fibrosis. LSM and AGILE 3+ outperformed both NFS and FIB-4 for fibrotic NASH (area under the receiver operating characteristic curve:LSM 0.79, AGILE 3+ 0.77, NFS 0.71, FIB-4 0.71; p < 0.001 of LSM-based versus simple serum tests). All noninvasive scores were suboptimal for diagnosing NASH. Conclusions: LSM and AGILE 3+ individually or in low availability settings in sequential combination after FIB-4 or NFS have a similar good diagnostic accuracy for advanced fibrosis and an acceptable diagnostic accuracy for fibrotic NASH in NAFLD patients with T2D.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Hepatology

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