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dc.contributor.authorMiller, Hamish
dc.contributor.authorHarman, David
dc.contributor.authorAithal, Guruprasad Padur
dc.contributor.authorManousou, Pinelopi
dc.contributor.authorCobbold, Jeremy F
dc.contributor.authorParker, Richard
dc.contributor.authorSheridan, David
dc.contributor.authorNewsome, Philip N
dc.contributor.authorKarpe, Fredrik
dc.contributor.authorNeville, Matthew
dc.contributor.authorArlt, Wiebke
dc.contributor.authorSitch, Alice J
dc.contributor.authorKorbonits, Marta
dc.contributor.authorBiehl, Michael
dc.contributor.authorAlazawi, William
dc.contributor.authorTomlinson, Jeremy W
dc.date.accessioned2024-03-06T15:05:41Z
dc.date.available2024-03-06T15:05:41Z
dc.date.issued2024-01-18
dc.identifier.citationMiller H, Harman D, Aithal GP, Manousou P, Cobbold JF, Parker R, Sheridan D, Newsome PN, Karpe F, Neville M, Arlt W, Sitch AJ, Korbonits M, Biehl M, Alazawi W, Tomlinson JW. Translating the potential of the urine steroid metabolome to stage NAFLD (TrUSt-NAFLD): study protocol for a multicentre, prospective validation study. BMJ Open. 2024 Jan 18;14(1):e074918. doi: 10.1136/bmjopen-2023-074918.en_US
dc.identifier.eissn2044-6055
dc.identifier.doi10.1136/bmjopen-2023-074918
dc.identifier.pmid38238179
dc.identifier.urihttp://hdl.handle.net/20.500.14200/3901
dc.description.abstractIntroduction: Non-alcoholic fatty liver disease (NAFLD) affects approximately one in four individuals and its prevalence continues to rise. The advanced stages of NAFLD with significant liver fibrosis are associated with adverse morbidity and mortality outcomes. Currently, liver biopsy remains the 'gold-standard' approach to stage NAFLD severity. Although generally well tolerated, liver biopsies are associated with significant complications, are resource intensive, costly, and sample only a very small area of the liver as well as requiring day case admission to a secondary care setting. As a result, there is a significant unmet need to develop non-invasive biomarkers that can accurately stage NAFLD and limit the need for liver biopsy. The aim of this study is to validate the use of the urine steroid metabolome as a strategy to stage NAFLD severity and to compare its performance against other non-invasive NAFLD biomarkers. Methods and analysis: The TrUSt-NAFLD study is a multicentre prospective test validation study aiming to recruit 310 patients with biopsy-proven and staged NAFLD across eight centres within the UK. 150 appropriately matched control patients without liver disease will be recruited through the Oxford Biobank. Blood and urine samples, alongside clinical data, will be collected from all participants. Urine samples will be analysed by liquid chromatography-tandem mass spectroscopy to quantify a panel of predefined steroid metabolites. A machine learning-based classifier, for example, Generalized Matrix Relevance Learning Vector Quantization that was trained on retrospective samples, will be applied to the prospective steroid metabolite data to determine its ability to identify those patients with advanced, as opposed to mild-moderate, liver fibrosis as a consequence of NAFLD. Ethics and dissemination: Research ethical approval was granted by West Midlands, Black Country Research Ethics Committee (REC reference: 21/WM/0177). A substantial amendment (TrUSt-NAFLD-SA1) was approved on 26 November 2021. Trial registration number: ISRCTN19370855.en_US
dc.language.isoenen_US
dc.publisherBMJ Publishing Groupen_US
dc.relation.urlhttp://bmjopen.bmj.com/en_US
dc.rights© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY. Published by BMJ.
dc.subjectEndocrinologyen_US
dc.titleTranslating the potential of the urine steroid metabolome to stage NAFLD (TrUSt-NAFLD): study protocol for a multicentre, prospective validation study.en_US
dc.typeArticle
dc.source.journaltitleBMJ Open
dc.source.volume14
dc.source.issue1
dc.source.beginpagee074918
dc.source.endpage
dc.source.countryUnited Kingdom
dc.source.countryEngland
rioxxterms.versionNAen_US
dc.contributor.trustauthorNewsome, Philip N
dc.contributor.departmentLiveren_US
dc.contributor.roleAdmin and Clericalen_US
oa.grant.openaccessnaen_US


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