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dc.contributor.authorTang, L. J.-
dc.contributor.authorSun, D. Q.-
dc.contributor.authorSong, S. J.-
dc.contributor.authorYip, T. C. F.-
dc.contributor.authorWong, G. L. H.-
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. S.-
dc.contributor.authorZheng, M. H.-
dc.date.accessioned2024-04-26T04:08:17Z-
dc.date.available2024-04-26T04:08:17Z-
dc.date.issued2024-
dc.identifier.citationLiver International 44(5):1129-1141, 2024-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/9530-
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.-
dc.subjectNephrology-
dc.subjectHepatology-
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.doihttps://dx.doi.org/10.1111/liv.15878-
dc.subject.keywordsrenal insufficiency, chronic-
dc.subject.keywordschronic kidney failure-
dc.subject.keywordsfatty liver-
dc.subject.keywordsfibrosis-
dc.subject.keywordskidney fibrosis-
dc.subject.keywordsliver disease-
dc.subject.keywordsliver fibrosis-
dc.subject.keywordsnon-alcoholic fatty liver disease-
dc.identifier.journaltitleLiver International-
dc.identifier.departmentGastroenterology and Hepatology-
dc.contributor.wslhdEslam, Mohammed-
dc.contributor.wslhdGeorge, Jacob-
dc.type.studyortrialCohort Analysis-
dc.type.studyortrialControlled Study-
dc.type.studyortrialDiagnostic Test Accuracy Study-
dc.type.studyortrialMajor Clinical Study-
dc.type.studyortrialRetrospective Study-
dc.identifier.pmid38426611-
dc.identifier.affiliationMAFLD Research Center, Department of Hepatology, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China-
dc.identifier.affiliationCancer Center, Faculty of Health Sciences, University of Macau, SAR, Taipa, Macao-
dc.identifier.affiliationDepartment of Nephrology, Jiangnan University Medical Center, Wuxi, China-
dc.identifier.affiliationAffiliated Wuxi Clinical College of Nantong University, Wuxi, China-
dc.identifier.affiliationDepartment of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong-
dc.identifier.affiliationState Key Laboratory of Digestive Disease, The Chinese University of Hong Kong, Hong Kong-
dc.identifier.affiliationDepartment of Laboratory Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China-
dc.identifier.affiliationDepartment of Pathology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China-
dc.identifier.affiliationNordic Bioscience Biomarkers and Research A/S, Herlev, Denmark-
dc.identifier.affiliationFosun Diagnostics Co., Ltd, Shanghai, China-
dc.identifier.affiliationMOE Frontier Science Centre for Precision Oncology, University of Macau, SAR, Taipa, Macao-
dc.identifier.affiliationSouthampton National Institute for Health and Care Research, Biomedical Research Centre, University of Southampton and University Hospital Southampton, Southampton, United Kingdom-
dc.identifier.affiliationDepartment of Medicine, University of Verona, Verona, Italy-
dc.identifier.affiliationIRCCS Sacro Cuore Don Calabria Hospital, Negrar di Valpolicella, Italy-
dc.identifier.affiliationStorr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital, Westmead, NSW, Australia-
dc.identifier.affiliationUniversity of Sydney, Sydney, NSW, Australia-
dc.identifier.affiliationInstitute of Hepatology, Wenzhou Medical University, Wenzhou, China-
dc.identifier.affiliationKey Laboratory of Diagnosis and Treatment for the Development of Chronic Liver Disease in Zhejiang Province, Wenzhou, China-
dc.identifier.facilityBlacktown-
dc.identifier.facilityWestmead-
Appears in Collections:Blacktown Mount Druitt Hospital

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