Factores de riesgo médicos y sociales para la progresión de la infección tuberculosa latente a tuberculosis activa en niños en contacto intradomiciliario en Uzbekistán: un estudio prospectivo
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Introducción: La infección tuberculosa latente (ITBL) se caracteriza por una respuesta inmunitaria sostenida a antígenos de Mycobacterium tuberculosis sin evidencia clínica, radiográfica ni microbiológica de enfermedad activa. El objetivo de este estudio fue evaluar los factores de riesgo médicos y sociales para la progresión de la infección tuberculosa latente (ITBL) a tuberculosis pulmonar activa en niños con contacto domiciliario con TB. Materiales y métodos: Estudio prospectivo (2022-2024) en el que participaron 120 niños de 4 a 12 años con ITBL. Se formaron dos grupos: niños que desarrollaron tuberculosis activa (grupo ITBL a tuberculosis) y aquellos que permanecieron latentes. La inclusión requirió consentimiento informado. Se analizaron factores clínicos, inmunológicos (IL-2, IgM) y sociales. El riesgo se evaluó mediante el riesgo relativo (RR) y sus intervalos de confianza del 95%. Resultados: La progresión a TB activa se relacionó con el contacto con TB bacilar (RR = 6,5), TB materna (RR = 5,2), anemia (RR = 3,8), >5 episodios de IRA/año (RR = 26,0), BCG ineficaz (RR = 3,0), hogares monoparentales (RR = 11,0), TB territorial (RR = 4,5), helmintiasis (RR = 10,0), varicela (RR = 5,0), enfermedades genitourinarias (RR = 8,0), patología otorrinolaringológica (RR = 5,7), monoterapia con isoniazida (RR = 2,7), exposición a COVID-19 o VIH (RR = 8,0), IL-2 >311,1 ng/ ml e IgM >1,18 UI/ml. Discusión: Los factores inmunológicos y sociales aumentan el riesgo de progresión de la ITBL. Los niños de alto riesgo necesitan un seguimiento personalizado.
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von Elm E, Altman DG, Egger M, et al. The Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) Statement: guidelines for reporting observational studies. Lancet. 2007;370(9596):1453-1457. https://doi.org/10.1016/S0140-6736(07)61602-X
World Medical Association. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. JAMA. 2013;310(20):2191-2194. https://doi.org/10.1001/jama.2013.281053
Slaseva DM, Petrushina AD, Brynza NS. Prognostication of latent tuberculosis infection and prevention of active tuberculosis forms in children and adolescents. Russ Pediatr J. 2022;3(1):289.
Belyan ZHE, Buinevich IV, Goponyako SV. Diagnostic methods for latent tuberculosis infection. Problemy Zdorov'ya i Ekologii. 2017;(3):9-14. https://doi.org/10.51523/2708-6011.2017-14-3-2
Shalayko TA. Comprehensive treatment of children at high risk of tuberculosis in a pediatric tuberculosis sanatorium. In: Current Issues in the Prevention, Diagnosis, and Treatment of Tuberculosis in Children and Adolescents. Abstracts of the 9th All-Russian Scientific and Practical Conference with International Participation; 2021; Moscow.
Kawahara JY, Irvine EB, Alter G. A case for antibodies as mechanistic correlates of immunity in tuberculosis. Front Immunol. 2019;10:996. https://doi.org/10.3389/fimmu.2019.00996
Jung YEG, Schluger NW. Advances in the diagnosis and treatment of latent tuberculosis infection. Curr Opin Infect Dis. 2020;33(2):166-72. https://doi.org/10.1097/QCO.0000000000000628
Xia Q, Wang H, Tang Y, Shi X, Gao L, Qin Y, et al. Is interleukin-2 an optimal marker for diagnosing tuberculosis infection? A systematic review and meta-analysis. Ann Med. 2020;52(7):376-85. https://doi.org/10.1080/07853890.2020.1800073
Esmail A, Randall P, Oelofse S, Tomasicchio M, Pooran A, Meldau R, et al. Comparison of two diagnostic intervention packages for communitybased active case finding for tuberculosis: an open-label randomized controlled trial. Nat Med. 2023;29(4):1009-16. https://doi.org/10.1038/s41591-023-02247-1
Essone PN, Leboueny M, Maloupazoa Siawaya AC, Alame-Emane AK, Aboumegone Biyogo OC, Dapnet Tadatsin PH, et al. Tuberculosis infection and antigen-specific cytokine response in healthcare workers frequently exposed to tuberculosis. Sci Rep. 2019;9:44294. https://doi.org/10.1038/s41598-019-44294-0
Mamishi S, Pourakbari B, Teymuri M, et al. Diagnostic accuracy of IL-2 for the diagnosis of latent tuberculosis: a systematic review and metaanalysis. Eur J Clin Microbiol Infect Dis. 2019;38(12):2111-9. https://doi.org/10.1007/s10096-014-2190-z
Barcellini L, Borroni E, Brown J, et al. First evaluation of QuantiFERON-TB Gold Plus performance in contact screening. Eur Respir J. 2016;48(5):1411-9. https://doi.org/10.1183/13993003.00282-2016
Meier NR, Jacobsen M, Ottenhoff THM, et al. A systematic review on novel Mycobacterium tuberculosis antigens and their discriminatory potential for the diagnosis of latent and active tuberculosis. Front Immunol. 2018;9:2476. https://doi.org/10.3389/fimmu.2018.02476
Tadolini M, Codecasa LR, García-García JM, et al. Active tuberculosis, sequelae and COVID-19 co-infection: first cohort of 49 cases. Eur Respir J. 2020;56(1):2001398. https://doi.org/10.1183/13993003.01398-2020
Liu Y, Bi L, Chen Y, et al. Active or latent tuberculosis increases susceptibility to COVID-19 and disease severity. MedRxiv. 2020. https://doi.org/10.1101/2020.03.10.20033795
Johns Hopkins University COVID-19 TB Research Group. Tuberculosis and COVID-19: lessons from the past and future perspectives. Clin Infect Dis. 2021;72(4):700-706. https://doi.org/10.1093/cid/ciaa314
Kumar NP, Sridhar R, Banurekha VV, et al. Effect of SARS-CoV-2 infection on immune response in latent tuberculosis infection. Front Immunol. 2023;14:1154320. https://doi.org/10.3389/fimmu.2023.1154320
World Health Organization. Latent tuberculosis infection: updated and consolidated guidelines for programmatic management. Geneva: WHO; 2018. Available from: https://www.who.int/publications/i/item/9789241550239