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The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies
Drug-induced liver injury (DILI) is a common adverse drug reaction leading to the interruption of tuberculosis (TB) therapy. We aimed to identify whether the hepatitis B virus (HBV) infection would increase the risk of DILI during first-line TB treatment. A meta-analysis of cohort studies searched i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cambridge University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770377/ https://www.ncbi.nlm.nih.gov/pubmed/33222713 http://dx.doi.org/10.1017/S0950268820002861 |
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author | Zheng, Jing Guo, Mei-Hong Peng, He-Wei Cai, Xiao-Ling Wu, Yun-Li Peng, Xian-E |
author_facet | Zheng, Jing Guo, Mei-Hong Peng, He-Wei Cai, Xiao-Ling Wu, Yun-Li Peng, Xian-E |
author_sort | Zheng, Jing |
collection | PubMed |
description | Drug-induced liver injury (DILI) is a common adverse drug reaction leading to the interruption of tuberculosis (TB) therapy. We aimed to identify whether the hepatitis B virus (HBV) infection would increase the risk of DILI during first-line TB treatment. A meta-analysis of cohort studies searched in PubMed, Web of Science and China National Knowledge Infrastructure was conducted. Effect sizes were reported as risk ratios (RRs) and 95% confidence intervals (CIs) and calculated by R software. Sixteen studies with 3960 TB patients were eligible for analysis. The risk of DILI appeared to be higher in TB patients co-infected with HBV (RR 2.66; 95% CI 2.13–3.32) than those without HBV infection. Moreover, patients with positive hepatitis B e antigen (HBeAg) were more likely to develop DILI (RR 3.42; 95% CI 1.95–5.98) compared to those with negative HBeAg (RR 2.30; 95% CI 1.66–3.18). Co-infection with HBV was not associated with a higher rate of anti-TB DILI in latent TB patients (RR 4.48; 95% CI 0.80–24.99). The effect of HBV infection on aggravating anti-TB DILI was independent of study participants, whether they were newly diagnosed with TB or not. Besides, TB and HBV co-infection patients had a longer duration of recovery from DILI compared to non-co-infected patients (SMD 2.26; 95% CI 1.87–2.66). To conclude, the results demonstrate that HBV infection would increase the risk of DILI during TB therapy, especially in patients with positive HBeAg, and close liver function monitoring is needed for TB and HBV co-infection patients. |
format | Online Article Text |
id | pubmed-7770377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cambridge University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77703772021-01-15 The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies Zheng, Jing Guo, Mei-Hong Peng, He-Wei Cai, Xiao-Ling Wu, Yun-Li Peng, Xian-E Epidemiol Infect Original Paper Drug-induced liver injury (DILI) is a common adverse drug reaction leading to the interruption of tuberculosis (TB) therapy. We aimed to identify whether the hepatitis B virus (HBV) infection would increase the risk of DILI during first-line TB treatment. A meta-analysis of cohort studies searched in PubMed, Web of Science and China National Knowledge Infrastructure was conducted. Effect sizes were reported as risk ratios (RRs) and 95% confidence intervals (CIs) and calculated by R software. Sixteen studies with 3960 TB patients were eligible for analysis. The risk of DILI appeared to be higher in TB patients co-infected with HBV (RR 2.66; 95% CI 2.13–3.32) than those without HBV infection. Moreover, patients with positive hepatitis B e antigen (HBeAg) were more likely to develop DILI (RR 3.42; 95% CI 1.95–5.98) compared to those with negative HBeAg (RR 2.30; 95% CI 1.66–3.18). Co-infection with HBV was not associated with a higher rate of anti-TB DILI in latent TB patients (RR 4.48; 95% CI 0.80–24.99). The effect of HBV infection on aggravating anti-TB DILI was independent of study participants, whether they were newly diagnosed with TB or not. Besides, TB and HBV co-infection patients had a longer duration of recovery from DILI compared to non-co-infected patients (SMD 2.26; 95% CI 1.87–2.66). To conclude, the results demonstrate that HBV infection would increase the risk of DILI during TB therapy, especially in patients with positive HBeAg, and close liver function monitoring is needed for TB and HBV co-infection patients. Cambridge University Press 2020-11-23 /pmc/articles/PMC7770377/ /pubmed/33222713 http://dx.doi.org/10.1017/S0950268820002861 Text en © The Author(s) 2020 http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Paper Zheng, Jing Guo, Mei-Hong Peng, He-Wei Cai, Xiao-Ling Wu, Yun-Li Peng, Xian-E The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies |
title | The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies |
title_full | The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies |
title_fullStr | The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies |
title_full_unstemmed | The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies |
title_short | The role of hepatitis B infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies |
title_sort | role of hepatitis b infection in anti-tuberculosis drug-induced liver injury: a meta-analysis of cohort studies |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7770377/ https://www.ncbi.nlm.nih.gov/pubmed/33222713 http://dx.doi.org/10.1017/S0950268820002861 |
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