Non‐invasive fibrosis markers for assessment of liver fibrosis in chronic hepatitis delta

Author:

Kalkan Çağdaş1ORCID,Yılmaz Yusufcan2ORCID,Erdoğan Beyza Doğanay3,Savaş Berna4,Yurdcu Esra5,Çalışkan Aysun1,Keskin Onur1,Gencdal Genco6,Zeybel Müjdat67,Törüner Murat1,Bozdayi A. Mithat5,Idilman Ramazan1,Yurdaydin Cihan16

Affiliation:

1. Department of Gastroenterology Ankara University Medical School Ankara Turkey

2. Department of Internal Medicine Ankara University Medical School Ankara Turkey

3. Department of Biostatistics Ankara University Medical School Ankara Turkey

4. Department of Pathology Ankara University Medical School Ankara Turkey

5. Hepatology Institute Ankara University Ankara Turkey

6. Department of Gastroenterology & Hepatology Koç University Medical School Istanbul Turkey

7. NIHR Nottingham Biomedical Research Centre Nottingham University Hospitals NHS Trust & University of Nottingham Nottingham UK

Abstract

AbstractAssessment of liver fibrosis by non‐invasive means is clinically important. Studies in chronic hepatitis delta (CHD) are scarce. We evaluated the performance of eight serum fibrosis markers [fibrosis‐4 score (FIB‐4), aspartate aminotransferase (AST) to alanine aminotransferase (ALT) ratio (AAR), age‐platelet index (API), AST‐to platelet‐ratio‐index (APRI), Goteborg University Cirrhosis Index (GUCI), Lok index, cirrhosis discriminant score (CDS) and Hui score] in CHD and chronic hepatitis B (CHB). Liver stiffness was assessed by transient elastography (TE) in CHD. The ability of fibrosis markers to detect significant fibrosis and cirrhosis were evaluated in 202 CHB and 108 CHD patients using published and new cut‐offs through receiver operating characteristics (ROC) analysis. The latter was also applied to obtain cut‐offs for TE. APRI, Fib‐4, API and Hui score were assessed for significant fibrosis, and APRI, GUCI, Lok index, CDS and AAR for cirrhosis determination. Fibrosis markers displayed weak performance in CHB for significant fibrosis with area under ROC (AUROC) curves between 0.62 and 0.71. They did slightly better for CHD. TE displayed an AUROC of 0.92 and performed better than serum fibrosis markers (p < 0.05 for fibrosis markers). For cirrhosis determination, CDS and Lok Index displayed an AUROC of 088 and 0.89 in CHB and GUCI, Lok index and APRI displayed AUROCs around 0.90 in CHD. TE displayed the best AUROC (0.95). Hence TE is superior to serum fibrosis markers for diagnosing significant liver fibrosis and cirrhosis. GUCI, Lok index and APRI displayed a reasonable performance in CHD, which needs further confirmation.

Publisher

Wiley

Subject

Virology,Infectious Diseases,Hepatology

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