4.4 Article

Construction of a mathematical model for tuberculosis transmission in highly endemic regions of the Asia-pacific

Journal

JOURNAL OF THEORETICAL BIOLOGY
Volume 358, Issue -, Pages 74-84

Publisher

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.jtbi.2014.05.023

Keywords

Models-Theoretical; Tuberculosis-Multidrug Resistant; Disease Transmission-Infectious; Latent tuberculosis; BCG vaccine

Funding

  1. National Health and Medical Research Postgraduate Scholarship
  2. National Health and Medical Research Council Career Development Fellowship
  3. Australian Government
  4. National Health and Medical Research Postgraduate Scholarship
  5. National Health and Medical Research Council Career Development Fellowship
  6. Australian Government

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We present a mathematical model to simulate tuberculosis (TB) transmission in highly endemic regions of the Asia-Pacific, where epidemiology does not appear to be primarily driven by HIV-coinfection. The ten-compartment deterministic model captures many of the observed phenomena important to disease dynamics, including partial and temporary vaccine efficacy, declining risk of active disease following infection, the possibility of reinfection both during the infection latent period and after treatment, multidrug resistant TB (MDR-TB) and de novo resistance during treatment. We found that the model could not be calibrated to the estimated incidence rate without allowing for reinfection during latency, and that even in the presence of a moderate fitness cost and a lower value of R-0, MDR-TB becomes the dominant strain at equilibrium. Of the modifiable programmatic parameters, the rate of detection and treatment commencement was the most important determinant of disease rates with each respective strain, while vaccination rates were less important. Improved treatment of drug-susceptible TB did not result in decreased rates of MDR-TB through prevention of de novo resistance, but rather resulted in a modest increase in MDR-TB through strain replacement. This was due to the considerably greater relative contribution of community transmission to MDR-TB incidence, by comparison to de novo amplification of resistance in previously susceptible strains. (C) 2014 The Authors. Published by Elsevier Ltd.

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