Quantifying progression and regression across the spectrum of pulmonary tuberculosis: a data synthesis study.


Journal

The Lancet. Global health
ISSN: 2214-109X
Titre abrégé: Lancet Glob Health
Pays: England
ID NLM: 101613665

Informations de publication

Date de publication:
05 2023
Historique:
received: 14 10 2022
revised: 30 01 2023
accepted: 06 02 2023
medline: 18 4 2023
pubmed: 27 3 2023
entrez: 26 3 2023
Statut: ppublish

Résumé

Prevalence surveys show a substantial burden of subclinical (asymptomatic but infectious) tuberculosis, from which individuals can progress, regress, or even persist in a chronic disease state. We aimed to quantify these pathways across the spectrum of tuberculosis disease. We created a deterministic framework of untreated tuberculosis disease with progression and regression between three states of pulmonary tuberculosis disease: minimal (non-infectious), subclinical (asymptomatic but infectious), and clinical (symptomatic and infectious). We obtained data from a previous systematic review of prospective and retrospective studies that followed and recorded the disease state of individuals with tuberculosis in a cohort without treatment. These data were considered in a Bayesian framework, enabling quantitative estimation of tuberculosis disease pathways with rates of transition between states and 95% uncertainty intervals (UIs). We included 22 studies with data from 5942 individuals in our analysis. Our model showed that after 5 years, 40% (95% UI 31·3-48·0) of individuals with prevalent subclinical disease at baseline recover and 18% (13·3-24·0) die from tuberculosis, with 14% (9·9-19·2) still having infectious disease, and the remainder with minimal disease at risk of re-progression. Over 5 years, 50% (40·0-59·1) of individuals with subclinical disease at baseline never develop symptoms. For those with clinical disease at baseline, 46% (38·3-52·2) die and 20% (15·2-25·8) recover from tuberculosis, with the remainder being in or transitioning between the three disease states after 5 years. We estimated the 10-year mortality of people with untreated prevalent infectious tuberculosis to be 37% (30·5-45·4). For people with subclinical tuberculosis, classic clinical disease is neither an inevitable nor an irreversible outcome. As such, reliance on symptom-based screening means a large proportion of people with infectious disease might never be detected. TB Modelling and Analysis Consortium and European Research Council.

Sections du résumé

BACKGROUND
Prevalence surveys show a substantial burden of subclinical (asymptomatic but infectious) tuberculosis, from which individuals can progress, regress, or even persist in a chronic disease state. We aimed to quantify these pathways across the spectrum of tuberculosis disease.
METHODS
We created a deterministic framework of untreated tuberculosis disease with progression and regression between three states of pulmonary tuberculosis disease: minimal (non-infectious), subclinical (asymptomatic but infectious), and clinical (symptomatic and infectious). We obtained data from a previous systematic review of prospective and retrospective studies that followed and recorded the disease state of individuals with tuberculosis in a cohort without treatment. These data were considered in a Bayesian framework, enabling quantitative estimation of tuberculosis disease pathways with rates of transition between states and 95% uncertainty intervals (UIs).
FINDINGS
We included 22 studies with data from 5942 individuals in our analysis. Our model showed that after 5 years, 40% (95% UI 31·3-48·0) of individuals with prevalent subclinical disease at baseline recover and 18% (13·3-24·0) die from tuberculosis, with 14% (9·9-19·2) still having infectious disease, and the remainder with minimal disease at risk of re-progression. Over 5 years, 50% (40·0-59·1) of individuals with subclinical disease at baseline never develop symptoms. For those with clinical disease at baseline, 46% (38·3-52·2) die and 20% (15·2-25·8) recover from tuberculosis, with the remainder being in or transitioning between the three disease states after 5 years. We estimated the 10-year mortality of people with untreated prevalent infectious tuberculosis to be 37% (30·5-45·4).
INTERPRETATION
For people with subclinical tuberculosis, classic clinical disease is neither an inevitable nor an irreversible outcome. As such, reliance on symptom-based screening means a large proportion of people with infectious disease might never be detected.
FUNDING
TB Modelling and Analysis Consortium and European Research Council.

Identifiants

pubmed: 36966785
pii: S2214-109X(23)00082-7
doi: 10.1016/S2214-109X(23)00082-7
pmc: PMC10126316
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e684-e692

Subventions

Organisme : Medical Research Council
ID : MR/V00476X/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 218261/Z/19/Z
Pays : United Kingdom

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license. Published by Elsevier Ltd.. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of interests FC coordinates a research project that received Xpert HR cartridges from Cepheid for evaluation of their utility for incipient tuberculosis. HE has participated on an advisory board for Cepheid concerning novel diagnostics with no payment or any other form of compensation received. All other authors declare no competing interests.

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Auteurs

Alexandra S Richards (AS)

TB Modelling Group, TB Centre, London School of Hygiene & Tropical Medicine, London, UK; Infectious Disease Epidemiology Department, London School of Hygiene & Tropical Medicine, London, UK. Electronic address: alexandra.richards@lshtm.ac.uk.

Bianca Sossen (B)

Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Jon C Emery (JC)

TB Modelling Group, TB Centre, London School of Hygiene & Tropical Medicine, London, UK; Infectious Disease Epidemiology Department, London School of Hygiene & Tropical Medicine, London, UK.

Katherine C Horton (KC)

TB Modelling Group, TB Centre, London School of Hygiene & Tropical Medicine, London, UK; Infectious Disease Epidemiology Department, London School of Hygiene & Tropical Medicine, London, UK.

Torben Heinsohn (T)

Institute for Global Health, University College London, London, UK; Helmholtz Centre for Infection Research, Braunschweig, Germany; German Centre for Infection Research, Braunschweig, Germany.

Beatrice Frascella (B)

School of Public Health, Vita-Salute San Raffaele University, Milan, Italy.

Federica Balzarini (F)

School of Public Health, Vita-Salute San Raffaele University, Milan, Italy; Local Health Authority of Bergamo, Bergamo, Italy.

Aurea Oradini-Alacreu (A)

School of Public Health, Vita-Salute San Raffaele University, Milan, Italy.

Brit Häcker (B)

Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.

Anna Odone (A)

German Central Committee Against Tuberculosis, Berlin, Germany.

Nicky McCreesh (N)

TB Modelling Group, TB Centre, London School of Hygiene & Tropical Medicine, London, UK; Infectious Disease Epidemiology Department, London School of Hygiene & Tropical Medicine, London, UK.

Alison D Grant (AD)

TB Centre, London School of Hygiene & Tropical Medicine, London, UK; Africa Health Research Institute, School of Laboratory Medicine and Medical Sciences, College of Health Sciences, University of KwaZulu-Natal, Durban, South Africa; School of Public Health, University of the Witwatersrand, Johannesburg, South Africa.

Katharina Kranzer (K)

Clinical Research Department, Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK; Biomedical Research and Training Institute, Harare, Zimbabwe; Division of Infectious Diseases and Tropical Medicine, University Hospital, Ludwig Maximilian University of Munich, Munich, Germany.

Frank Cobelens (F)

Department of Global Health and Amsterdam Institute for Global Health and Development, Amsterdam University Medical Centers, Amsterdam, Netherlands.

Hanif Esmail (H)

Wellcome Centre for Infectious Diseases Research in Africa, Institute of Infectious Diseases and Molecular Medicine, University of Cape Town, Cape Town, South Africa; Institute for Global Health, University College London, London, UK; MRC Clinical Trials Unit, University College London, London, UK.

Rein M G J Houben (RMGJ)

TB Modelling Group, TB Centre, London School of Hygiene & Tropical Medicine, London, UK; Infectious Disease Epidemiology Department, London School of Hygiene & Tropical Medicine, London, UK.

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