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dc.contributor.authorTang, L. J.-
dc.contributor.authorSun, D. Q.-
dc.contributor.authorSong, S. J.-
dc.contributor.authorYip, T. C.-
dc.contributor.authorWong, G. L.-
dc.contributor.authorZhu, P. W.-
dc.contributor.authorChen, S. D.-
dc.contributor.authorKarsdal, M.-
dc.contributor.authorLeeming, D. J.-
dc.contributor.authorJiang, P.-
dc.contributor.authorWang, C.-
dc.contributor.authorChen, Q.-
dc.contributor.authorByrne, C. D.-
dc.contributor.authorTargher, G.-
dc.contributor.authorEslam, Mohammed-
dc.contributor.authorGeorge, Jacob-
dc.contributor.authorWong, V. W.-
dc.contributor.authorZheng, M. H.-
dc.date.accessioned2024-05-16T03:11:28Z-
dc.date.available2024-05-16T03:11:28Z-
dc.date.issued2024-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/9640-
dc.description.abstractBACKGROUND: Metabolic dysfunction-associated fatty liver disease (MAFLD) is an emerging risk factor for chronic kidney disease (CKD). N-terminal propeptide of collagen type 3 (PRO-C3) is a biomarker of advanced fibrosis in MAFLD and PRO-C3 may be involved in renal fibrosis. We aimed to use PRO-C3 measurements to generate a new algorithmic score to test the prediction of MAFLD with chronic kidney disease (MAFLD-CKD). METHODS: A derivation and independent validation cohort of 750 and 129 Asian patients with biopsy-confirmed MAFLD were included. Serum PRO-C3 concentration was measured and regression analyses were performed to examine associations with MAFLD-CKD. A derivative algorithm for MAFLD-CKD risk prediction was evaluated with receiver operator characteristic (ROC) curve analysis. RESULTS: The study included two Asian cohorts (n = 180 with MAFLD-CKD; mean-eGFR: 94.93 mL/min/1.73 m2; median-urinary albumin-to-creatinine ratio: 6.58 mg/mmol). PRO-C3 was associated with the severity of MAFLD-CKD and independently associated with MAFLD-CKD (adjusted odds ratio = 1.16, 95% confidence interval [CI]: 1.08-1.23, p < .001). A new non-invasive score (termed PERIOD) including PRO-C3 efficiently predicted MAFLD-CKD (AUROC = .842, 95% CI: .805-.875). Accuracy, specificity and negative predictive values were 80.2%, 85.1% and 88.4%, respectively. In the validation cohort, the PERIOD score had good diagnostic performance (AUROC = .807, 95% CI: .691-.893) with similar results in all patient subgroups. In the MAFLD-CKD subgroup, the accuracy for identifying advanced fibrosis was further improved by combining the PRO-C3-based ADAPT with the Agile 3+ scores (AUROC = .90, 95% CI: .836-.964). CONCLUSIONS: The PERIOD score is helpful for accurately predicting the risk of MAFLD-CKD. PRO-C3 can also be used to assess liver fibrosis in people with MAFLD-CKD. Copyright 2024 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.-
dc.subjectComplement C3-
dc.subjectLiver Cirrhosis-
dc.subjectNon-alcoholic Fatty Liver Disease-
dc.subjectRenal Insufficiency, Chronic-
dc.subjectAsian People-
dc.titleSerum PRO-C3 is useful for risk prediction and fibrosis assessment in MAFLD with chronic kidney disease in an Asian cohort-
dc.typeJournal Article-
dc.identifier.doiStorr Liver Centre-
dc.identifier.journaltitleLiver International-
dc.identifier.departmentLiver International 44(5):1129-1141, 2024-
dc.contributor.wslhdEslam, Mohammed-
dc.contributor.wslhdGeorge, Jacob-
dc.identifier.pmid38426611-
dc.identifier.facilityWestmead-
Appears in Collections:Westmead Hospital 2019 - 2024

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