Multiple exposures, reinfection and risk of progression to active tuberculosis

Author:

Ackley Sarah F.12ORCID,Lee Robyn S.3,Worden Lee2,Zwick Erin4,Porco Travis C.125,Behr Marcel A.67,Pepperell Caitlin S.8

Affiliation:

1. Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA

2. Proctor Foundation, University of California, San Francisco, CA, USA

3. Department of Epidemiology, Harvard University, School of Public Health, Boston, MA, USA

4. Department of Population Health Sciences, University of Wisconsin – Madison, School of Medicine and Public Health, Madison, WI, USA

5. Department of Ophthalmology, University of California, San Francisco, CA, USA

6. Department of Medicine, McGill University, Montreal, Quebec, Canada

7. McGill International TB Centre, Montreal, Quebec, Canada

8. Medicine and Medical Microbiology and Immunology, University of Wisconsin – Madison, Madison, WI, USA

Abstract

A recent study reported on a tuberculosis (TB) outbreak in a largely Inuit village. Among newly infected individuals, exposure to additional active cases was associated with an increasing probability of developing active disease within a year. Using binomial risk models, we evaluated two potential mechanisms by which multiple infections during the first year following initial infection could account for increasing disease risk with increasing exposures. In the reinfection model , each infectious contact confers an independent risk of an infection, and infections contribute independently to active disease. In the threshold model , disease risk follows a sigmoidal function with small numbers of infectious contacts conferring a low risk of active disease and large numbers of contacts conferring a high risk. To determine the dynamic impact of reinfection during the early phase of infection, we performed simulations from a modified Reed–Frost model of TB dynamics following spread from an initial number of cases. We parametrized this model with the maximum-likelihood estimates from the reinfection and threshold models in addition to the observed distribution of exposures among new infections. We find that both models can plausibly account for the observed increase in disease risk with increasing infectious contacts, but the threshold model confers a better fit than a nested model without a threshold ( p = 0.04). Our simulations indicate that multiple exposures to infectious individuals during this critical time period can lead to dramatic increases in outbreak size. In order to decrease TB burden in high-prevalence settings, it may be necessary to implement measures aimed at preventing repeated exposures, in addition to preventing primary infection.

Funder

Canadian Institutes of Health Research

National Institute of Allergy and Infectious Diseases

National Institute of General Medical Sciences

NIH Research Training for Computation and Informatics

Publisher

The Royal Society

Subject

Multidisciplinary

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