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Study design for development of novel safety biomarkers of drug-induced liver injury by the translational safety biomarker pipeline (TransBioLine) consortium : a study protocol for a nested case-control study

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dc.contributor.author TransBioLine consortium
dc.date.accessioned 2023-10-21T01:08:15Z
dc.date.available 2023-10-21T01:08:15Z
dc.date.issued 2023-09-12
dc.identifier.citation TransBioLine consortium 2023 , ' Study design for development of novel safety biomarkers of drug-induced liver injury by the translational safety biomarker pipeline (TransBioLine) consortium : a study protocol for a nested case-control study ' , Diagnostic and prognostic research , vol. 7 , no. 1 , pp. 18 . https://doi.org/10.1186/s41512-023-00155-z
dc.identifier.issn 2397-7523
dc.identifier.other 197603631
dc.identifier.other 17b9151c-0d2a-4c32-9d51-74e60fbfc3fd
dc.identifier.other 37697410
dc.identifier.other PubMedCentral: PMC10496294
dc.identifier.other unpaywall: 10.1186/s41512-023-00155-z
dc.identifier.uri https://hdl.handle.net/20.500.11815/4513
dc.description © 2023. BioMed Central Ltd., part of Springer Nature.
dc.description.abstract A lack of biomarkers that detect drug-induced liver injury (DILI) accurately continues to hinder early- and late-stage drug development and remains a challenge in clinical practice. The Innovative Medicines Initiative's TransBioLine consortium comprising academic and industry partners is developing a prospective repository of deeply phenotyped cases and controls with biological samples during liver injury progression to facilitate biomarker discovery, evaluation, validation and qualification.In a nested case-control design, patients who meet one of these criteria, alanine transaminase (ALT) ≥ 5 × the upper limit of normal (ULN), alkaline phosphatase ≥ 2 × ULN or ALT ≥ 3 ULN with total bilirubin > 2 × ULN, are enrolled. After completed clinical investigations, Roussel Uclaf Causality Assessment and expert panel review are used to adjudicate episodes as DILI or alternative liver diseases (acute non-DILI controls). Two blood samples are taken: at recruitment and follow-up. Sample size is as follows: 300 cases of DILI and 130 acute non-DILI controls. Additional cross-sectional cohorts (1 visit) are as follows: Healthy volunteers (n = 120), controls with chronic alcohol-related or non-alcoholic fatty liver disease (n = 100 each) and patients with psoriasis or rheumatoid arthritis (n = 100, 50 treated with methotrexate) are enrolled. Candidate biomarkers prioritised for evaluation include osteopontin, glutamate dehydrogenase, cytokeratin-18 (full length and caspase cleaved), macrophage-colony-stimulating factor 1 receptor and high mobility group protein B1 as well as bile acids, sphingolipids and microRNAs. The TransBioLine project is enabling biomarker discovery and validation that could improve detection, diagnostic accuracy and prognostication of DILI in premarketing clinical trials and for clinical healthcare application.
dc.format.extent 1989125
dc.format.extent 18
dc.language.iso en
dc.relation.ispartofseries Diagnostic and prognostic research; 7(1)
dc.rights info:eu-repo/semantics/openAccess
dc.subject Meltingarlæknisfræði
dc.title Study design for development of novel safety biomarkers of drug-induced liver injury by the translational safety biomarker pipeline (TransBioLine) consortium : a study protocol for a nested case-control study
dc.type /dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article
dc.description.version Peer reviewed
dc.identifier.doi 10.1186/s41512-023-00155-z
dc.contributor.department Other departments
dc.contributor.department Faculty of Medicine


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