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      Tuberculosis infection and disease in South African adolescents with perinatally acquired HIV on antiretroviral therapy: a cohort study

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          Abstract

          Introduction

          There are limited data on Tuberculosis (TB) in adolescents with perinatally acquired HIV (APHIV). We examined the incidence and determinants of TB infection and disease in the Cape Town Adolescent Antiretroviral Cohort (CTAAC).

          Methods

          Youth between nine and fourteen years on antiretroviral therapy (ART) for more than six months in public sector care, and age‐matched HIV‐negative adolescents, were enrolled between July 2013 through March 2015 and followed six‐monthly. Data were censored on 31 October 2018. Symptom screening, chest radiograph, viral load, CD4 count, QuantiFERON (QFT) and sputum for Xpert MTB/RIF, microscopy, culture and sensitivity were performed annually. TB infection was defined by a QFT of >0.35 IU/mL. TB diagnosis was defined as confirmed (culture or Xpert MTB/RIF positive) or unconfirmed (clinical diagnosis and started on TB treatment). Analyses examined the incidence and determinants of TB infection and disease.

          Results

          Overall 496 HIV+ and 103 HIV‐negative participants (median age at enrolment 12 years (interquartile range, IQR 10.6 to 13.3) were followed for a median of 3.1 years (IQR 3.0 to 3.4); 50% (298/599) were male. APHIV initiated ART at median age 4.4 years (IQR 2.1 to 7.6). At enrolment, 376/496 (76%) had HIV viral load <40 copies/mL, median CD4 count was 713 cells/mm 3 and 179/559 (32%) were QFT+, with no difference by HIV status (APHIV 154/468, 33%; HIV negative 25/91, 27%; p = 0.31). The cumulative QFT+ prevalence was similar (APHIV 225/492, 46%; 95%CI 41% to 50%; HIV negative 44/98, 45%; 95% CI 35% to 55%; p = 0.88). APHIV had a higher incidence of all TB disease than HIV‐negative adolescents (2.2/100PY, 95% CI 1.6 to 3.1 vs. 0.3/100PY, 95% CI 0.04 to 2.2; IRR 7.36, 95% CI 1.01 to 53.55). The rate of bacteriologically confirmed TB in APHIV was 1.3/100 PY compared to 0.3/100PY for HIV‐negative adolescents, suggesting a fourfold increased risk of developing TB disease in APHIV despite access to ART. In addition, a positive QFT at enrolment was not predictive of TB in this population.

          Conclusions

          High incidence rates of TB disease occur in APHIV despite similar QFT conversion rates to HIV‐negative adolescents. Strategies to prevent TB in this vulnerable group must be strengthened.

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          Most cited references25

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          The natural history of childhood intra-thoracic tuberculosis: a critical review of literature from the pre-chemotherapy era.

          The pre-chemotherapy literature documented the natural history of tuberculosis in childhood. These disease descriptions remain invaluable for guiding public health policy and research, as the introduction of effective chemotherapy radically changed the history of disease. Specific high-risk groups were identified. Primary infection before 2 years of age frequently progressed to serious disease within the first 12 months without significant prior symptoms. Primary infection between 2 and 10 years of age rarely progressed to serious disease, and such progression was associated with significant clinical symptoms. In children aged >3 years the presence of symptoms represented a window of opportunity in which to establish a clinical diagnosis before serious disease progression. Primary infection after 10 years of age frequently progressed to adult-type disease. Early effective intervention in this group will reduce the burden of cavitating disease and associated disease transmission in the community. Although the pre-chemotherapy literature excluded the influence of human immune deficiency virus (HIV) infection, recent disease descriptions in HIV-infected children indicate that immune-compromised children behave in a similar fashion to immune immature children (less than 2 years of age). An important concept deduced from the natural history of tuberculosis in childhood is that of relevant disease. Deciding which children to treat may be extremely difficult in high-prevalence, low-resource settings. The concept of relevant disease provides guidance for more effective public health intervention.
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            Evaluation of tuberculosis diagnostics in children: 1. Proposed clinical case definitions for classification of intrathoracic tuberculosis disease. Consensus from an expert panel.

            There is a critical need for improved diagnosis of tuberculosis in children, particularly in young children with intrathoracic disease as this represents the most common type of tuberculosis in children and the greatest diagnostic challenge. There is also a need for standardized clinical case definitions for the evaluation of diagnostics in prospective clinical research studies that include children in whom tuberculosis is suspected but not confirmed by culture of Mycobacterium tuberculosis. A panel representing a wide range of expertise and child tuberculosis research experience aimed to develop standardized clinical research case definitions for intrathoracic tuberculosis in children to enable harmonized evaluation of new tuberculosis diagnostic technologies in pediatric populations. Draft definitions and statements were proposed and circulated widely for feedback. An expert panel then considered each of the proposed definitions and statements relating to clinical definitions. Formal group consensus rules were established and consensus was reached for each statement. The definitions presented in this article are intended for use in clinical research to evaluate diagnostic assays and not for individual patient diagnosis or treatment decisions. A complementary article addresses methodological issues to consider for research of diagnostics in children with suspected tuberculosis.
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              The prognosis of a positive tuberculin reaction in childhood and adolescence.

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                Author and article information

                Contributors
                frigati@sun.ac.za
                Journal
                J Int AIDS Soc
                J Int AIDS Soc
                10.1002/(ISSN)1758-2652
                JIA2
                Journal of the International AIDS Society
                John Wiley and Sons Inc. (Hoboken )
                1758-2652
                14 March 2021
                March 2021
                : 24
                : 3 ( doiID: 10.1002/jia2.v24.3 )
                : e25671
                Affiliations
                [ 1 ] Department of Paediatrics and Child Health University of Cape Town Cape South Africa
                [ 2 ] Family Center for Research with Ubuntu (FAMCRU) Department of Paediatrics and Child Health Stellenbosch University Cape Town South Africa
                [ 3 ] Wellcome Centre for Infectious Disease Research in Africa Institute of Infectious Disease and Molecular Medicine University of Cape Town Cape Town South Africa
                [ 4 ] The Francis Crick Institute London United Kingdom
                [ 5 ] Division of Epidemiology and Biostatistics School of Public Health and Family Medicine University of Cape Town Cape Town South Africa
                [ 6 ] Department of Pediatric Pulmonology, Immunology and Intensive Care Medicine Charité ‐ Universitätsmedizin Berlin Berlin Germany
                [ 7 ] Berlin Institute of Health Berlin Germany
                [ 8 ] SAMRC Unit on Child and Adolescent Health University of Cape Town Cape Town South Africa
                Author notes
                [*] [* ] Corresponding author: Lisa J Frigati, Research Centre for Adolescent and Child Health (REACH) and Medical Research (MRC) Unit on Child and Adolescent Health, University of Cape Town Department of Pediatrics and Child Health, Rondebosch 7700, Cape Town, South Africa. Tel: +27 216 585 111. ( frigati@ 123456sun.ac.za )

                Author information
                https://orcid.org/0000-0002-4097-3128
                https://orcid.org/0000-0001-8882-698X
                https://orcid.org/0000-0003-0480-0868
                https://orcid.org/0000-0003-2559-6034
                Article
                JIA225671
                10.1002/jia2.25671
                7957181
                33719199
                c6ab46f3-1a2d-4ac3-b9a4-9d88e7f6037c
                © 2021 The Authors. Journal of the International AIDS Society published by John Wiley & Sons Ltd on behalf of the International AIDS Society.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 December 2020
                : 27 August 2020
                : 27 January 2021
                Page count
                Figures: 3, Tables: 5, Pages: 11, Words: 7975
                Funding
                Funded by: NIH , open-funder-registry 10.13039/100000002;
                Award ID: R01HD074051
                Funded by: Bongani Mayosi National Health Scholars Program
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                March 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.9 mode:remove_FC converted:15.03.2021

                Infectious disease & Microbiology
                tuberculosis,coinfection,incidence,adolescents,perinatal,hiv
                Infectious disease & Microbiology
                tuberculosis, coinfection, incidence, adolescents, perinatal, hiv

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