Metabolic‐associated fatty liver disease is associated with acute pancreatitis with more severe course: Post hoc analysis of a prospectively collected international registry

Author:

Váncsa Szilárd123ORCID,Sipos Zoltán14,Váradi Alex156ORCID,Nagy Rita127,Ocskay Klementina17,Juhász Félix Márk17,Márta Katalin23,Teutsch Brigitta12,Mikó Alexandra18,Hegyi Péter Jenő123ORCID,Vincze Áron9,Izbéki Ferenc10,Czakó László11,Papp Mária12,Hamvas József13,Varga Márta14,Török Imola15,Mickevicius Artautas1617ORCID,Erőss Bálint123,Párniczky Andrea127ORCID,Szentesi Andrea118,Pár Gabriella19,Hegyi Péter12318ORCID,

Affiliation:

1. Institute for Translational Medicine Medical School University of Pécs Pécs Hungary

2. Centre for Translational Medicine Semmelweis University Budapest Hungary

3. Institute of Pancreatic Diseases Semmelweis University Budapest Hungary

4. Institute of Bioanalysis Medical School University of Pécs Pécs Hungary

5. Department of Metagenomics University of Debrecen Debrecen Hungary

6. Department of Laboratory Medicine Medical School University of Pécs Pécs Hungary

7. Heim Pál National Pediatric Institute Budapest Hungary

8. Department of Medical Genetics Medical School University of Pécs Pécs Hungary

9. Division of Gastroenterology First Department of Medicine Medical School University of Pécs Pécs Hungary

10. Szent György University Teaching Hospital of Fejér County Székesfehérvár Hungary

11. Department of Medicine Albert Szent‐Györgyi Medical School University of Szeged Szeged Hungary

12. Department of Gastroenterology Institute of Internal Medicine Faculty of Medicine University of Debrecen Debrecen Hungary

13. Peterfy Hospital Budapest Hungary

14. Department of Gastroenterology BMKK Dr. Réthy Pál Hospital Békéscsaba Hungary

15. County Emergency Clinical Hospital of Targu Mures ‐ Gastroenterology and George Emil Palade University of Medicine Pharmacy, Science and Technology of Targu Mures Targu Mures Romania

16. Vilnius University Hospital Santaros Clinics Vilnius Lithuania

17. Clinics of Abdominal Surgery, Nephrology and Gastroenterology Faculty of Medicine Vilnius University Vilnius Lithuania

18. Translational Pancreatology Research Group Interdisciplinary Centre of Excellence for Research Development and Innovation University of Szeged Szeged Hungary

Abstract

AbstractIntroductionNon‐alcoholic fatty liver disease (NAFLD) is a proven risk factor for acute pancreatitis (AP). However, NAFLD has recently been redefined as metabolic‐associated fatty liver disease (MAFLD). In this post hoc analysis, we quantified the effect of MAFLD on the outcomes of AP.MethodsWe identified our patients from the multicentric, prospective International Acute Pancreatitis Registry of the Hungarian Pancreatic Study Group. Next, we compared AP patients with and without MAFLD and the individual components of MAFLD regarding in‐hospital mortality and AP severity based on the revised Atlanta classification. Lastly, we calculated odds ratios (ORs) with 95% confidence intervals (CIs) using multivariate logistic regression analysis.ResultsMAFLD had a high prevalence in AP, 39% (801/2053). MAFLD increased the odds of moderate‐to‐severe AP (OR = 1.43, CI: 1.09–1.89). However, the odds of in‐hospital mortality (OR = 0.89, CI: 0.42–1.89) and severe AP (OR = 1.70, CI: 0.97–3.01) were not higher in the MAFLD group. Out of the three diagnostic criteria of MAFLD, the highest odds of severe AP was in the group based on metabolic risk abnormalities (OR = 2.68, CI: 1.39–5.09). In addition, the presence of one, two, and three diagnostic criteria dose‐dependently increased the odds of moderate‐to‐severe AP (OR = 1.23, CI: 0.88–1.70, OR = 1.38, CI: 0.93–2.04, and OR = 3.04, CI: 1.63–5.70, respectively) and severe AP (OR = 1.13, CI: 0.54–2.27, OR = 2.08, CI: 0.97–4.35, and OR = 4.76, CI: 1.50–15.4, respectively). Furthermore, in patients with alcohol abuse and aged ≥60 years, the effect of MAFLD became insignificant.ConclusionsMAFLD is associated with AP severity, which varies based on the components of its diagnostic criteria. Furthermore, MAFLD shows a dose‐dependent effect on the outcomes of AP.

Publisher

Wiley

Subject

Gastroenterology,Oncology

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