Publication:
Age as a Confounding Factor for the Accurate Non-Invasive Diagnosis of Advanced NAFLD Fibrosis.

cris.virtualsource.author-orcid1db177e5-b0b4-4b1c-b039-8b18d729f454
datacite.rightsopen.access
dc.contributor.authorMcPherson, Stuart
dc.contributor.authorHardy, Tim
dc.contributor.authorDufour, Jean-François
dc.contributor.authorPetta, Salvatore
dc.contributor.authorRomero-Gomez, Manuel
dc.contributor.authorAllison, Mike
dc.contributor.authorOliveira, Claudia P
dc.contributor.authorFrancque, Sven
dc.contributor.authorVan Gaal, Luc
dc.contributor.authorSchattenberg, Jörn M
dc.contributor.authorTiniakos, Dina
dc.contributor.authorBurt, Alastair
dc.contributor.authorBugianesi, Elisabetta
dc.contributor.authorRatziu, Vlad
dc.contributor.authorDay, Christopher P
dc.contributor.authorAnstee, Quentin M
dc.date.accessioned2024-10-24T19:02:33Z
dc.date.available2024-10-24T19:02:33Z
dc.date.issued2017-05
dc.description.abstractOBJECTIVES Non-invasive fibrosis scores are widely used to identify/exclude advanced fibrosis in patients with non-alcoholic fatty liver disease (NAFLD). However, these scores were principally developed and validated in patients aged between 35 and 65 years of age. The objective of this study was to assess the effect of age on the performance of non-invasive fibrosis tests in NAFLD. METHODS Patients were recruited from European specialist hepatology clinics. The cohort was divided into five age-based groups: ≤35 (n=74), 36-45 (n=96), 46-55 (n=197), 56-64 (n=191), and ≥65 years (n=76), and the performance of the aspartate aminotransferase (AST)/alanine transaminase (ALT) ratio, fibrosis 4 (FIB-4), and NAFLD fibrosis score (NFS) for advanced fibrosis (stage F3-F4) for each group was assessed using liver biopsy as the standard. RESULTS Six hundred and thirty-four patients were included. The diagnostic accuracy of the AST/ALT ratio was lower than NFS and FIB-4 in all the age groups. The AST/ALT ratio, NFS, and FIB-4 score performed poorly for a diagnosis of advanced fibrosis in those aged ≤35 years (area under the receiver operating characteristic curves (AUROCs 0.52, 0.52, and 0.60, respectively). For all groups >35 years, AUROCs for advanced fibrosis were similar for the NFS and FIB-4 score (range 0.77-0.84). However, the specificity for advanced fibrosis using the FIB-4 and NFS declined with age, becoming unacceptably low in those aged ≥65 years (35% for FIB-4 and 20% for NFS). New cutoffs were derived (and validated) for those aged ≥65 years, which improved specificity to 70% without adversely affecting sensitivity (FIB-4 2.0, sensitivity 77%; NFS 0.12, sensitivity 80%). CONCLUSIONS The NFS and FIB-4 scores have similar accuracy for advanced fibrosis in patients aged >35 years. However, the specificity for advanced fibrosis is unacceptably low in patients aged ≥65 years, resulting in a high false positive rate. New thresholds for use in patients aged ≥65 years are proposed to address this issue.Am J Gastroenterol advance online publication, 11 October 2016; doi:10.1038/ajg.2016.453.
dc.description.numberOfPages12
dc.description.sponsorshipDepartement Klinische Forschung, Hepatologie Forschung
dc.identifier.doi10.7892/boris.93541
dc.identifier.pmid27725647
dc.identifier.publisherDOI10.1038/ajg.2016.453
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/148432
dc.language.isoen
dc.publisherNature Publishing Group
dc.relation.ispartofThe American journal of gastroenterology
dc.relation.issn1572-0241
dc.relation.organizationDCD5A442BBC5E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442C6DFE17DE0405C82790C4DE2
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleAge as a Confounding Factor for the Accurate Non-Invasive Diagnosis of Advanced NAFLD Fibrosis.
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage751
oaire.citation.issue5
oaire.citation.startPage740
oaire.citation.volume112
oairecerif.author.affiliationDepartement Klinische Forschung, Hepatologie Forschung
oairecerif.author.affiliation2Universitätsklinik für Viszerale Chirurgie und Medizin, Hepatologie
oairecerif.author.affiliation3Universitätsklinik für Viszerale Chirurgie und Medizin, Hepatologie
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unibe.eprints.legacyId93541
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unibe.subtype.articlejournal

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