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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

Authors :
Jane I. Grove
Camilla Stephens
M. Isabel Lucena
Raúl J. Andrade
Sabine Weber
Alexander Gerbes
Einar S. Bjornsson
Guido Stirnimann
Ann K. Daly
Matthias Hackl
Kseniya Khamina-Kotisch
Jose J. G. Marin
Maria J. Monte
Sara A. Paciga
Melanie Lingaya
Shiva S. Forootan
Christopher E. P. Goldring
Oliver Poetz
Rudolf Lombaard
Alexandra Stege
Helgi K. Bjorrnsson
Mercedes Robles-Diaz
Dingzhou Li
Thi Dong Binh Tran
Shashi K. Ramaiah
Sophia L. Samodelov
Gerd A. Kullak-Ublick
Guruprasad P. Aithal
on behalf of the TransBioLine consortium
Source :
Diagnostic and Prognostic Research, Vol 7, Iss 1, Pp 1-15 (2023)
Publication Year :
2023
Publisher :
BMC, 2023.

Abstract

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.

Subjects

Subjects :
Medicine (General)
R5-920

Details

Language :
English
ISSN :
23977523
Volume :
7
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Diagnostic and Prognostic Research
Publication Type :
Academic Journal
Accession number :
edsdoj.01c9031ea63844faa64609c76d355eda
Document Type :
article
Full Text :
https://doi.org/10.1186/s41512-023-00155-z