Publication:
Non-invasive fibrosis markers for assessment of liver fibrosis in chronic hepatitis delta

dc.contributor.coauthorKalkan, Çağdaş
dc.contributor.coauthorYılmaz, Yusufcan
dc.contributor.coauthorErdoğan, Beyza Doğanay
dc.contributor.coauthorSavaş, Berna
dc.contributor.coauthorYurdcu, Esra
dc.contributor.coauthorÇalışkan, Aysun
dc.contributor.coauthorKeskin, Onur
dc.contributor.coauthorTörüner, Murat
dc.contributor.coauthorBozdayi, A. Mithat
dc.contributor.coauthorIdilman, Ramazan
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorGençdal, Genco
dc.contributor.kuauthorYurdaydın, Süleyman Cihan
dc.contributor.kuauthorZeybel, Müjdat
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:04:35Z
dc.date.issued2023
dc.description.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.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.indexedbyWOS
dc.description.openaccessYES
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.WoSQuartileQ3
dc.identifier.doi10.1111/jvh.13806
dc.identifier.eissn1365-2893
dc.identifier.embargoN/A
dc.identifier.endpage416
dc.identifier.issn1352-0504
dc.identifier.issue5
dc.identifier.pubmed36651603
dc.identifier.scopus2-s2.0-85147505829
dc.identifier.startpage406
dc.identifier.urihttps://doi.org/10.1111/jvh.13806
dc.identifier.urihttps://hdl.handle.net/20.500.14288/8664
dc.identifier.volume30
dc.identifier.wos000928876300001
dc.keywordsChronic hepatitis B
dc.keywordsChronic hepatitis delta
dc.keywordsSerum fibrosis markers
dc.keywordsTransient elastography
dc.language.isoeng
dc.publisherWiley
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofJournal of Viral Hepatitis
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectGastroenterology
dc.subjectHepatology
dc.subjectInfectious diseases
dc.subjectVirology
dc.titleNon-invasive fibrosis markers for assessment of liver fibrosis in chronic hepatitis delta
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorYurtaydın, Süleyman Cihan
local.contributor.kuauthorGençdal, Genco
local.contributor.kuauthorZeybel, Müjdat
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