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      Transmissibility and potential for disease progression of drug resistant Mycobacterium tuberculosis: prospective cohort study

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          Abstract

          Objective

          To measure the association between phenotypic drug resistance and the risk of tuberculosis infection and disease among household contacts of patients with pulmonary tuberculosis.

          Setting

          106 district health centers in Lima, Peru between September 2009 and September 2012.

          Design

          Prospective cohort study.

          Participants

          10 160 household contacts of 3339 index patients with tuberculosis were classified on the basis of the drug resistance profile of the patient: 6189 were exposed to drug susceptible strains of Mycobacterium tuberculosis, 1659 to strains resistant to isoniazid or rifampicin, and 1541 to strains that were multidrug resistant (resistant to isoniazid and rifampicin).

          Main outcome measures

          Tuberculosis infection (positive tuberculin skin test) and the incidence of active disease (diagnosed by positive sputum smear or chest radiograph) after 12 months of follow-up.

          Results

          Household contacts exposed to patients with multidrug resistant tuberculosis had an 8% (95% confidence interval 4% to 13%) higher risk of infection by the end of follow-up compared with household contacts of patients with drug sensitive tuberculosis. The relative hazard of incident tuberculosis disease did not differ among household contacts exposed to multidrug resistant tuberculosis and those exposed to drug sensitive tuberculosis (adjusted hazard ratio 1.28, 95% confidence interval 0.9 to 1.83).

          Conclusion

          Household contacts of patients with multidrug resistant tuberculosis were at higher risk of tuberculosis infection than contacts exposed to drug sensitive tuberculosis. The risk of developing tuberculosis disease did not differ among contacts in both groups. The evidence invites guideline producers to take action by targeting drug resistant and drug sensitive tuberculosis, such as early detection and effective treatment of infection and disease.

          Trial registration

          ClinicalTrials.gov NCT00676754.

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          Most cited references35

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          The biological cost of antibiotic resistance.

          The frequency and rates of ascent and dissemination of antibiotic resistance in bacterial populations are anticipated to be directly related to the volume of antibiotic use and inversely related to the cost that resistance imposes on the fitness of bacteria. The data available from recent laboratory studies suggest that most, but not all, resistance-determining mutations and accessory elements engender some fitness cost, but those costs are likely to be ameliorated by subsequent evolution.
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            The competitive cost of antibiotic resistance in Mycobacterium tuberculosis.

            Mathematical models predict that the future of the multidrug-resistant tuberculosis epidemic will depend on the fitness cost of drug resistance. We show that in laboratory-derived mutants of Mycobacterium tuberculosis, rifampin resistance is universally associated with a competitive fitness cost and that this cost is determined by the specific resistance mutation and strain genetic background. In contrast, we demonstrate that prolonged patient treatment can result in multidrug-resistant strains with no fitness defect and that strains with low- or no-cost resistance mutations are also the most frequent among clinical isolates.
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              • Article: not found

              Transmission of multidrug-resistant Mycobacterium tuberculosis in Shanghai, China: a retrospective observational study using whole-genome sequencing and epidemiological investigation.

              Multidrug-resistance is a substantial threat to global elimination of tuberculosis. Understanding transmission patterns is crucial for control of the disease. We used a genomic and epidemiological approach to assess recent transmission of multidrug-resistant (MDR) tuberculosis and identify potential risk factors for transmission.
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                Author and article information

                Contributors
                Role: professor
                Role: instructor
                Role: executive director
                Role: public health adviser
                Role: director of programs
                Role: director of laboratory and pharmacy
                Role: head of data management center
                Role: assistant professor
                Role: programmer/analyst
                Role: director of research computing
                Role: professor
                Role: associate professor
                Role: professor and chair
                Role: professor
                Journal
                BMJ
                BMJ
                BMJ-UK
                bmj
                The BMJ
                BMJ Publishing Group Ltd.
                0959-8138
                1756-1833
                2019
                24 October 2019
                : 367
                : l5894
                Affiliations
                [1 ]Department of Global Health and Social Medicine, Harvard Medical School, 641 Huntington Avenue, Boston, MA 02115, USA
                [2 ]Division of Global Health Equity, Department of Medicine, Brigham and Women’s Hospital, Boston, MA, USA
                [3 ]Socios En Salud, Lima, Peru
                [4 ]World Bank, Washington, DC, USA
                [5 ]School of Social Work, College of Behavioral and Community Sciences, University of South Florida, Tampa, FL, USA
                [6 ]Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT, USA
                Author notes
                Correspondence to: M Murray megan_murray@ 123456hms.harvard.edu (or @megan_b_murray on Twitter)
                Author information
                http://orcid.org/0000-0003-0443-1986
                Article
                berm050973
                10.1136/bmj.l5894
                6812583
                31649017
                35078d61-5449-442c-a330-7d1da4e7c357
                Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions

                This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 16 September 2019
                Categories
                Research

                Medicine
                Medicine

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