Abstract

Global stakeholders including the World Health Organization rely on predictive models for developing strategies and setting targets for tuberculosis care and control programs. Failure to account for variation in individual risk leads to substantial biases that impair data interpretation and policy decisions. Anticipated impediments to estimating heterogeneity for each parameter are discouraging despite considerable technical progress in recent years. Here we identify acquisition of infection as the single process where heterogeneity most fundamentally impacts model outputs, due to selection imposed by dynamic forces of infection. We introduce concrete metrics of risk inequality, demonstrate their utility in mathematical models, and pack the information into a risk inequality coefficient (RIC) which can be calculated and reported by national tuberculosis programs for use in policy development and modeling.

Highlights

  • Global stakeholders including the World Health Organization rely on predictive models for developing strategies and setting targets for tuberculosis care and control programs

  • The Lorenz curves corresponding to the discretization, which are depicted by the dashed lines in Fig. 1a, are used as an approximation to the original solid curves with the same risk inequality coefficient (RIC)

  • Measures of statistical dispersion are commonly used in economics to represent the distribution of wealth among individuals in a country and to compare inequality between countries, but rarely used in epidemiology[33,34]

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Summary

Introduction

Global stakeholders including the World Health Organization rely on predictive models for developing strategies and setting targets for tuberculosis care and control programs. The premise is that variation in the risk of acquiring a disease (whether infectious or not) goes beyond what is captured by measured factors (typically age, malnutrition, comorbidities, habits, social contacts, etc), and a distribution of unobserved heterogeneity can be inferred from incidence trends in a holistic manner. Such distributions are needed for eliminating biases in interpretation and prediction[12,13], and can be utilized in conjunction with more common reductionist approaches, which are required when there is desire to target interventions at individuals with specific characteristics. Forasmuch as individuals are nonuniformly distributed, disease incidence will vary between groups and carry information about variation in individual risks

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