Whole genome sequencing of M. tuberculosis for disease control in high-burden settings: study protocol for a cluster randomized controlled trial evaluating different community-wide intervention strategies in rural Madagascar.


Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
25 Oct 2024
Historique:
received: 15 05 2024
accepted: 07 10 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 26 10 2024
Statut: epublish

Résumé

Retrospective and descriptive molecular epidemiology studies have shown that Mycobacterium tuberculosis whole genome sequencing can identify outbreaks and disease transmission events with higher resolution than conventional epidemiological investigations. Those studies have strengthened our understanding of genomic polymorphisms correlating with person-to-person transmission and helped resolve putative transmission clusters. To date, systematic genomic surveillance programs implemented for M. tuberculosis were only implemented in low-incidence settings. The purpose of this study is to determine whether there is an impact of routine M. tuberculosis whole genome sequencing on tuberculosis case detection in a high-incidence setting. A cluster randomized controlled trial will be performed. Forty-eight rural village groups (or Fokontany) in the Vohibato district of Madagascar will be randomized to one of three interventions arms. Arm 1 (standard of care) involves healthcare facility-based passive case detection with smear microscopy testing. Arm 2 (best practice) consists of active case finding and Xpert MTB/RIF Ultra PCR testing followed by household contact investigations. Arm 3 (novel intervention) includes the same interventions as arm 2, with addition of sputum culture and M. tuberculosis whole genome sequencing for all newly diagnosed cases. In arm 3, molecular suggested putative outbreaks are investigated, and additional TB suspects are appropriately tested. The intervention observational period will be 2 years. The primary outcome will be the number of detected cases/100,000/year in each arm after 1 year of intervention. This study is designed to determine whether there is an impact of prospective whole genome sequencing-based molecular typing on tuberculosis case detection in high-incidence settings. Investigating potential outbreaks and focusing active case finding in spatiotemporal settings where disease transmission is suggested by genomic typing is hypothesized to improve case detection in rural communities. ClinicalTrials.gov NCT05406453 . Retrospectively registered on June 6, 2022.

Sections du résumé

BACKGROUND BACKGROUND
Retrospective and descriptive molecular epidemiology studies have shown that Mycobacterium tuberculosis whole genome sequencing can identify outbreaks and disease transmission events with higher resolution than conventional epidemiological investigations. Those studies have strengthened our understanding of genomic polymorphisms correlating with person-to-person transmission and helped resolve putative transmission clusters. To date, systematic genomic surveillance programs implemented for M. tuberculosis were only implemented in low-incidence settings. The purpose of this study is to determine whether there is an impact of routine M. tuberculosis whole genome sequencing on tuberculosis case detection in a high-incidence setting.
METHODS METHODS
A cluster randomized controlled trial will be performed. Forty-eight rural village groups (or Fokontany) in the Vohibato district of Madagascar will be randomized to one of three interventions arms. Arm 1 (standard of care) involves healthcare facility-based passive case detection with smear microscopy testing. Arm 2 (best practice) consists of active case finding and Xpert MTB/RIF Ultra PCR testing followed by household contact investigations. Arm 3 (novel intervention) includes the same interventions as arm 2, with addition of sputum culture and M. tuberculosis whole genome sequencing for all newly diagnosed cases. In arm 3, molecular suggested putative outbreaks are investigated, and additional TB suspects are appropriately tested. The intervention observational period will be 2 years. The primary outcome will be the number of detected cases/100,000/year in each arm after 1 year of intervention.
DISCUSSION CONCLUSIONS
This study is designed to determine whether there is an impact of prospective whole genome sequencing-based molecular typing on tuberculosis case detection in high-incidence settings. Investigating potential outbreaks and focusing active case finding in spatiotemporal settings where disease transmission is suggested by genomic typing is hypothesized to improve case detection in rural communities.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov NCT05406453 . Retrospectively registered on June 6, 2022.

Identifiants

pubmed: 39456079
doi: 10.1186/s13063-024-08537-4
pii: 10.1186/s13063-024-08537-4
doi:

Banques de données

ClinicalTrials.gov
['NCT05406453']

Types de publication

Journal Article Clinical Trial Protocol

Langues

eng

Sous-ensembles de citation

IM

Pagination

717

Informations de copyright

© 2024. The Author(s).

Références

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Auteurs

Emmanuelle Sandra Adjoa Ametepe (ESA)

École de Santé Publique de L'Université de Montréal (ESPUM), Université de Montréal, Montréal, Canada.
Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Université de Montréal, Montréal, Canada.

Noela Andriamanoha (N)

Epidemiology Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar.

Fanantenana Randria Andrianomanana (FR)

Mycobacteria Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar.

Floriane Point (F)

Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Université de Montréal, Montréal, Canada.

Reziky Tiandraza Mangahasimbola (RT)

Epidemiology Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar.

Alina Dyachenko (A)

Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Université de Montréal, Montréal, Canada.

Michael Hall (M)

European Bioinformatics Institute (EMBL-EBI), Cambridgeshire, UK.
The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, Melbourne, Australia.

Theodora Mayouya Gamana (TM)

Epidemiology Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar.

Astrid M Knoblauch (AM)

Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
University of Basel, Basel, Switzerland.

Yemimah Yededyah Razafindrasoa (YY)

Epidemiology Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar.

Arianminpathy Nimalan (A)

School of Public Health, Imperial College, London, England.

Marcel Behr (M)

Research Instituteof the, McGill University Health Center , Montreal, Canada.

Madeleine Durand (M)

Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Université de Montréal, Montréal, Canada.
Department of Medicine, Université de Montréal, Montréal, Canada.

Mira Johri (M)

École de Santé Publique de L'Université de Montréal (ESPUM), Université de Montréal, Montréal, Canada.
Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Université de Montréal, Montréal, Canada.

Zamin Iqbal (Z)

European Bioinformatics Institute (EMBL-EBI), Cambridgeshire, UK.
Milner Center for Evolution, University of Bath, Bath, UK.

Andry Rivo Rakotoarivelo (AR)

Department of Medicine, Université de Montréal, Montréal, Canada.

Rindra Vatosoa Randremanana (RV)

Epidemiology Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar.

Niaina Rakotosamimanana (N)

Mycobacteria Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar.

Simon Grandjean Lapierre (SG)

Centre de Recherche du Centre Hospitalier de L'Université de Montréal, Université de Montréal, Montréal, Canada. simon.grandjean.lapierre@umontreal.ca.
Mycobacteria Unit, Institut Pasteur de Madagascar, Ambohitrakely, Antananarivo, Madagascar. simon.grandjean.lapierre@umontreal.ca.
Department of Microbiology, Immunology and Infectious Diseases, Université de Montréal, Montréal, Canada. simon.grandjean.lapierre@umontreal.ca.

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