Cargando…

A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment

Objectives: To establish an individualized nomogram to predict the probability of drug-induced liver injury (DILI) in tuberculosis patients receiving anti-tuberculosis treatment. Methods: The clinical information of patients admitted to a tertiary hospital between January 2010 and December 2022 was...

Descripción completa

Detalles Bibliográficos
Autores principales: Ji, Songjun, Lu, Bin, Pan, Xinling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232814/
https://www.ncbi.nlm.nih.gov/pubmed/37274095
http://dx.doi.org/10.3389/fphar.2023.1153815
_version_ 1785052076214059008
author Ji, Songjun
Lu, Bin
Pan, Xinling
author_facet Ji, Songjun
Lu, Bin
Pan, Xinling
author_sort Ji, Songjun
collection PubMed
description Objectives: To establish an individualized nomogram to predict the probability of drug-induced liver injury (DILI) in tuberculosis patients receiving anti-tuberculosis treatment. Methods: The clinical information of patients admitted to a tertiary hospital between January 2010 and December 2022 was retrospectively reviewed from the clinical records. Patients with baseline liver diseases (hepatis B or C infection and fatty liver) or taking liver protective drugs were excluded. The maximum values in liver function test within 180 days after anti-tuberculosis treatment were collected to determine the occurrence of DILI. The candidate variables used for establishing prediction model in this study were the last results within the 30 days before the treatment onset. The final variables were included after univariate and multivariate logistic regression analyses and applied to establish the nomogram model. The discrimination power and prediction accuracy of the prediction model were assessed using the area under the receiver operating characteristic (AUC) curve and a calibration chart. The clinical effectiveness was assessed via decision curve analysis (DCA). The established model was validated in two validation groups. Results: A total of 1979 patients with 25 variables were enrolled in this study, and the incidence of DILI was 4.2% (n = 83). The patients with complete variables were divided into training group (n = 1,121), validation group I (n = 492) and validation group II (n = 264). Five variables were independent factors for DILI and included in the final prediction model presented as nomogram: age (odds ratio [OR] 1.022, p = 0.023), total bilirubin ≥17.1 μmol/L (OR 11.714, p < 0.001), uric acid (OR 0.977, p = 0.047), neutrophil count (OR 2.145, 0.013) and alcohol consumption (OR 3.209, p = 0.002). The AUCs of the prediction model in the training group, validation group I and validation group II were 0.833, 0.668, and 0.753, respectively. The p-values of calibration charts in the three groups were 0.800, 0.996, and 0.853. The DCA curves of the prediction model were above the two extreme curves. Conclusion: The nomogram model in this study could effectively predict the DILI risk among patients under anti-tuberculosis drug treatment.
format Online
Article
Text
id pubmed-10232814
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-102328142023-06-02 A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment Ji, Songjun Lu, Bin Pan, Xinling Front Pharmacol Pharmacology Objectives: To establish an individualized nomogram to predict the probability of drug-induced liver injury (DILI) in tuberculosis patients receiving anti-tuberculosis treatment. Methods: The clinical information of patients admitted to a tertiary hospital between January 2010 and December 2022 was retrospectively reviewed from the clinical records. Patients with baseline liver diseases (hepatis B or C infection and fatty liver) or taking liver protective drugs were excluded. The maximum values in liver function test within 180 days after anti-tuberculosis treatment were collected to determine the occurrence of DILI. The candidate variables used for establishing prediction model in this study were the last results within the 30 days before the treatment onset. The final variables were included after univariate and multivariate logistic regression analyses and applied to establish the nomogram model. The discrimination power and prediction accuracy of the prediction model were assessed using the area under the receiver operating characteristic (AUC) curve and a calibration chart. The clinical effectiveness was assessed via decision curve analysis (DCA). The established model was validated in two validation groups. Results: A total of 1979 patients with 25 variables were enrolled in this study, and the incidence of DILI was 4.2% (n = 83). The patients with complete variables were divided into training group (n = 1,121), validation group I (n = 492) and validation group II (n = 264). Five variables were independent factors for DILI and included in the final prediction model presented as nomogram: age (odds ratio [OR] 1.022, p = 0.023), total bilirubin ≥17.1 μmol/L (OR 11.714, p < 0.001), uric acid (OR 0.977, p = 0.047), neutrophil count (OR 2.145, 0.013) and alcohol consumption (OR 3.209, p = 0.002). The AUCs of the prediction model in the training group, validation group I and validation group II were 0.833, 0.668, and 0.753, respectively. The p-values of calibration charts in the three groups were 0.800, 0.996, and 0.853. The DCA curves of the prediction model were above the two extreme curves. Conclusion: The nomogram model in this study could effectively predict the DILI risk among patients under anti-tuberculosis drug treatment. Frontiers Media S.A. 2023-05-18 /pmc/articles/PMC10232814/ /pubmed/37274095 http://dx.doi.org/10.3389/fphar.2023.1153815 Text en Copyright © 2023 Ji, Lu and Pan. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Ji, Songjun
Lu, Bin
Pan, Xinling
A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment
title A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment
title_full A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment
title_fullStr A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment
title_full_unstemmed A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment
title_short A nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment
title_sort nomogram model to predict the risk of drug-induced liver injury in patients receiving anti-tuberculosis treatment
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232814/
https://www.ncbi.nlm.nih.gov/pubmed/37274095
http://dx.doi.org/10.3389/fphar.2023.1153815
work_keys_str_mv AT jisongjun anomogrammodeltopredicttheriskofdruginducedliverinjuryinpatientsreceivingantituberculosistreatment
AT lubin anomogrammodeltopredicttheriskofdruginducedliverinjuryinpatientsreceivingantituberculosistreatment
AT panxinling anomogrammodeltopredicttheriskofdruginducedliverinjuryinpatientsreceivingantituberculosistreatment
AT jisongjun nomogrammodeltopredicttheriskofdruginducedliverinjuryinpatientsreceivingantituberculosistreatment
AT lubin nomogrammodeltopredicttheriskofdruginducedliverinjuryinpatientsreceivingantituberculosistreatment
AT panxinling nomogrammodeltopredicttheriskofdruginducedliverinjuryinpatientsreceivingantituberculosistreatment