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The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis

BACKGROUND: Children (<15 years) are vulnerable to TB disease following infection, but no systematic review or meta-analysis has quantified the effects of HIV-related immunosuppression or antiretroviral therapy (ART) on their TB incidence. OBJECTIVES: Determine the impact of HIV infection and ART...

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Autores principales: Dodd, P J, Prendergast, A J, Beecroft, C, Kampmann, B, Seddon, J A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520282/
https://www.ncbi.nlm.nih.gov/pubmed/28115682
http://dx.doi.org/10.1136/thoraxjnl-2016-209421
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author Dodd, P J
Prendergast, A J
Beecroft, C
Kampmann, B
Seddon, J A
author_facet Dodd, P J
Prendergast, A J
Beecroft, C
Kampmann, B
Seddon, J A
author_sort Dodd, P J
collection PubMed
description BACKGROUND: Children (<15 years) are vulnerable to TB disease following infection, but no systematic review or meta-analysis has quantified the effects of HIV-related immunosuppression or antiretroviral therapy (ART) on their TB incidence. OBJECTIVES: Determine the impact of HIV infection and ART on risk of incident TB disease in children. METHODS: We searched MEDLINE and Embase for studies measuring HIV prevalence in paediatric TB cases (‘TB cohorts’) and paediatric HIV cohorts reporting TB incidence (‘HIV cohorts’). Study quality was assessed using the Newcastle-Ottawa tool. TB cohorts with controls were meta-analysed to determine the incidence rate ratio (IRR) for TB given HIV. HIV cohort data were meta-analysed to estimate the trend in log-IRR versus CD4%, relative incidence by immunological stage and ART-associated protection from TB. RESULTS: 42 TB cohorts and 22 HIV cohorts were included. In the eight TB cohorts with controls, the IRR for TB was 7.9 (95% CI 4.5 to 13.7). HIV-infected children exhibited a reduction in IRR of 0.94 (95% credible interval: 0.83–1.07) per percentage point increase in CD4%. TB incidence was 5.0 (95% CI 4.0 to 6.0) times higher in children with severe compared with non-significant immunosuppression. TB incidence was lower in HIV-infected children on ART (HR: 0.30; 95% CI 0.21 to 0.39). Following initiation of ART, TB incidence declined rapidly over 12 months towards a HR of 0.10 (95% CI 0.04 to 0.25). CONCLUSIONS: HIV is a potent risk factor for paediatric TB, and ART is strongly protective. In HIV-infected children, early diagnosis and ART initiation reduces TB risk. TRIAL REGISTRATION NUMBER: CRD42014014276.
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spelling pubmed-55202822017-07-31 The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis Dodd, P J Prendergast, A J Beecroft, C Kampmann, B Seddon, J A Thorax Tuberculosis BACKGROUND: Children (<15 years) are vulnerable to TB disease following infection, but no systematic review or meta-analysis has quantified the effects of HIV-related immunosuppression or antiretroviral therapy (ART) on their TB incidence. OBJECTIVES: Determine the impact of HIV infection and ART on risk of incident TB disease in children. METHODS: We searched MEDLINE and Embase for studies measuring HIV prevalence in paediatric TB cases (‘TB cohorts’) and paediatric HIV cohorts reporting TB incidence (‘HIV cohorts’). Study quality was assessed using the Newcastle-Ottawa tool. TB cohorts with controls were meta-analysed to determine the incidence rate ratio (IRR) for TB given HIV. HIV cohort data were meta-analysed to estimate the trend in log-IRR versus CD4%, relative incidence by immunological stage and ART-associated protection from TB. RESULTS: 42 TB cohorts and 22 HIV cohorts were included. In the eight TB cohorts with controls, the IRR for TB was 7.9 (95% CI 4.5 to 13.7). HIV-infected children exhibited a reduction in IRR of 0.94 (95% credible interval: 0.83–1.07) per percentage point increase in CD4%. TB incidence was 5.0 (95% CI 4.0 to 6.0) times higher in children with severe compared with non-significant immunosuppression. TB incidence was lower in HIV-infected children on ART (HR: 0.30; 95% CI 0.21 to 0.39). Following initiation of ART, TB incidence declined rapidly over 12 months towards a HR of 0.10 (95% CI 0.04 to 0.25). CONCLUSIONS: HIV is a potent risk factor for paediatric TB, and ART is strongly protective. In HIV-infected children, early diagnosis and ART initiation reduces TB risk. TRIAL REGISTRATION NUMBER: CRD42014014276. BMJ Publishing Group 2017-06 2017-01-23 /pmc/articles/PMC5520282/ /pubmed/28115682 http://dx.doi.org/10.1136/thoraxjnl-2016-209421 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Tuberculosis
Dodd, P J
Prendergast, A J
Beecroft, C
Kampmann, B
Seddon, J A
The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis
title The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis
title_full The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis
title_fullStr The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis
title_full_unstemmed The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis
title_short The impact of HIV and antiretroviral therapy on TB risk in children: a systematic review and meta-analysis
title_sort impact of hiv and antiretroviral therapy on tb risk in children: a systematic review and meta-analysis
topic Tuberculosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5520282/
https://www.ncbi.nlm.nih.gov/pubmed/28115682
http://dx.doi.org/10.1136/thoraxjnl-2016-209421
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