Emergence of additional drug resistance during treatment of multidrug-resistant tuberculosis in China: a prospective cohort study.


Journal

Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
ISSN: 1469-0691
Titre abrégé: Clin Microbiol Infect
Pays: England
ID NLM: 9516420

Informations de publication

Date de publication:
Dec 2021
Historique:
received: 18 09 2020
revised: 30 03 2021
accepted: 06 04 2021
pubmed: 26 4 2021
medline: 13 1 2022
entrez: 25 4 2021
Statut: ppublish

Résumé

Little is known about how additional second-line drug resistance emerges during multidrug-resistant tuberculosis (MDR-TB) treatment. The present study aimed to investigate the influence of microevolution, exogenous reinfection and mixed infection on second-line drug resistance during the recommended 2-year MDR-TB treatment. Individuals with MDR-TB were enrolled between 2013 and 2016 in a multicentre prospective observational cohort study and were followed up for 2 years until treatment completion. Whole-genome sequencing (WGS) was applied for serial Mycobacterium tuberculosis isolates from study participants throughout the treatment, to study the role of microevolution, exogenous reinfection and mixed infection in the development of second-line drug resistance. Of the 286 enrolled patients with MDR-TB, 63 (22.0%) M. tuberculosis isolates developed additional drug resistance during the MDR-TB treatment, including 5 that fulfilled the criteria of extensively drug-resistant TB. By comparing WGS data of serial isolates retrieved from the patients throughout treatment, 41 (65.1%) of the cases of additional second-line drug resistance were the result of exogenous reinfection, 18 (28.6%) were caused by acquired drug resistance, i.e. microevolution, while the remaining 4 (6.3%) were caused by mixed infections with drug-resistant and drug-susceptible strains. In multivariate analysis, previous TB treatment (adjusted hazard ratio (aHR) 2.51, 95% CI 1.51-4.18), extensive disease on chest X-ray (aHR 3.39, 95% CI 2.03-5.66) and type 2 diabetes mellitus (aHR 4.00, 95% CI 2.22-7.21) were independent risk factors associated with the development of additional second-line drug resistance. A large proportion of additional second-line drug resistance emerging during MDR-TB treatment was attributed to exogenous reinfection, indicating the urgency of infection control in health facilities as well as the need for repeated drug susceptibility testing throughout MDR-TB treatment.

Identifiants

pubmed: 33895338
pii: S1198-743X(21)00169-5
doi: 10.1016/j.cmi.2021.04.001
pii:
doi:

Substances chimiques

Antitubercular Agents 0

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1805-1813

Informations de copyright

Copyright © 2021 European Society of Clinical Microbiology and Infectious Diseases. Published by Elsevier Ltd. All rights reserved.

Auteurs

Yi Hu (Y)

Department of Epidemiology, School of Public Health and Key Laboratory of Public Health Safety, Fudan University, Shanghai, China.

Xubin Zheng (X)

Department of Epidemiology, School of Public Health and Key Laboratory of Public Health Safety, Fudan University, Shanghai, China.

Lina Davies Forsman (L)

Division of Infectious Diseases, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden; Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.

Zhu Ning (Z)

Zigong City Centre for Disease Control and Prevention, Zigong, Sichuan, China.

Cheng Chen (C)

Jiangsu Provincial Centre for Disease Control and Prevention, Nanjing, Jiangsu, China.

Yazhou Gao (Y)

Department of Epidemiology, School of Public Health and Key Laboratory of Public Health Safety, Fudan University, Shanghai, China.

Zhengdong Zhang (Z)

Zigong City Centre for Disease Control and Prevention, Zigong, Sichuan, China.

Wei Lu (W)

Jiangsu Provincial Centre for Disease Control and Prevention, Nanjing, Jiangsu, China.

Jim Werngren (J)

Department of Microbiology, The Public Health Agency of Sweden, Stockholm, Sweden.

Judith Bruchfeld (J)

Division of Infectious Diseases, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden; Department of Infectious Diseases, Karolinska University Hospital, Stockholm, Sweden.

Sven Hoffner (S)

Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.

Biao Xu (B)

Department of Epidemiology, School of Public Health and Key Laboratory of Public Health Safety, Fudan University, Shanghai, China. Electronic address: bxu@shmu.edu.cn.

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