Cargando…

Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment?

Drug induced liver injury (DILI) is a potentially serious adverse reaction in a few susceptible individuals under therapy by various drugs. Health care professionals facing DILI are confronted with a wealth of drug-unrelated liver diseases with high incidence and prevalence rates, which can confound...

Descripción completa

Detalles Bibliográficos
Autores principales: Teschke, Rolf, Schulze, Johannes, Eickhoff, Axel, Danan, Gaby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412387/
https://www.ncbi.nlm.nih.gov/pubmed/28398242
http://dx.doi.org/10.3390/ijms18040803
_version_ 1783232989622173696
author Teschke, Rolf
Schulze, Johannes
Eickhoff, Axel
Danan, Gaby
author_facet Teschke, Rolf
Schulze, Johannes
Eickhoff, Axel
Danan, Gaby
author_sort Teschke, Rolf
collection PubMed
description Drug induced liver injury (DILI) is a potentially serious adverse reaction in a few susceptible individuals under therapy by various drugs. Health care professionals facing DILI are confronted with a wealth of drug-unrelated liver diseases with high incidence and prevalence rates, which can confound the DILI diagnosis. Searching for alternative causes is a key element of RUCAM (Roussel Uclaf Causality Assessment Method) to assess rigorously causality in suspected DILI cases. Diagnostic biomarkers as blood tests would be a great help to clinicians, regulators, and pharmaceutical industry would be more comfortable if, in addition to RUCAM, causality of DILI can be confirmed. High specificity and sensitivity are required for any diagnostic biomarker. Although some risk factors are available to evaluate liver safety of drugs in patients, no valid diagnostic or prognostic biomarker exists currently for idiosyncratic DILI when a liver injury occurred. Identifying a biomarker in idiosyncratic DILI requires detailed knowledge of cellular and biochemical disturbances leading to apoptosis or cell necrosis and causing leakage of specific products in blood. As idiosyncratic DILI is typically a human disease and hardly reproducible in animals, pathogenetic events and resulting possible biomarkers remain largely undisclosed. Potential new diagnostic biomarkers should be evaluated in patients with DILI and RUCAM-based established causality. In conclusion, causality assessment in cases of suspected idiosyncratic DILI is still best achieved using RUCAM since specific biomarkers as diagnostic blood tests that could enhance RUCAM results are not yet available.
format Online
Article
Text
id pubmed-5412387
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-54123872017-05-05 Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment? Teschke, Rolf Schulze, Johannes Eickhoff, Axel Danan, Gaby Int J Mol Sci Review Drug induced liver injury (DILI) is a potentially serious adverse reaction in a few susceptible individuals under therapy by various drugs. Health care professionals facing DILI are confronted with a wealth of drug-unrelated liver diseases with high incidence and prevalence rates, which can confound the DILI diagnosis. Searching for alternative causes is a key element of RUCAM (Roussel Uclaf Causality Assessment Method) to assess rigorously causality in suspected DILI cases. Diagnostic biomarkers as blood tests would be a great help to clinicians, regulators, and pharmaceutical industry would be more comfortable if, in addition to RUCAM, causality of DILI can be confirmed. High specificity and sensitivity are required for any diagnostic biomarker. Although some risk factors are available to evaluate liver safety of drugs in patients, no valid diagnostic or prognostic biomarker exists currently for idiosyncratic DILI when a liver injury occurred. Identifying a biomarker in idiosyncratic DILI requires detailed knowledge of cellular and biochemical disturbances leading to apoptosis or cell necrosis and causing leakage of specific products in blood. As idiosyncratic DILI is typically a human disease and hardly reproducible in animals, pathogenetic events and resulting possible biomarkers remain largely undisclosed. Potential new diagnostic biomarkers should be evaluated in patients with DILI and RUCAM-based established causality. In conclusion, causality assessment in cases of suspected idiosyncratic DILI is still best achieved using RUCAM since specific biomarkers as diagnostic blood tests that could enhance RUCAM results are not yet available. MDPI 2017-04-11 /pmc/articles/PMC5412387/ /pubmed/28398242 http://dx.doi.org/10.3390/ijms18040803 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Teschke, Rolf
Schulze, Johannes
Eickhoff, Axel
Danan, Gaby
Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment?
title Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment?
title_full Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment?
title_fullStr Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment?
title_full_unstemmed Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment?
title_short Drug Induced Liver Injury: Can Biomarkers Assist RUCAM in Causality Assessment?
title_sort drug induced liver injury: can biomarkers assist rucam in causality assessment?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5412387/
https://www.ncbi.nlm.nih.gov/pubmed/28398242
http://dx.doi.org/10.3390/ijms18040803
work_keys_str_mv AT teschkerolf druginducedliverinjurycanbiomarkersassistrucamincausalityassessment
AT schulzejohannes druginducedliverinjurycanbiomarkersassistrucamincausalityassessment
AT eickhoffaxel druginducedliverinjurycanbiomarkersassistrucamincausalityassessment
AT danangaby druginducedliverinjurycanbiomarkersassistrucamincausalityassessment