Impact of imperfect test sensitivity on determining risk factors: the case of bovine tuberculosis

PLoS One. 2012;7(8):e43116. doi: 10.1371/journal.pone.0043116. Epub 2012 Aug 13.

Abstract

Background: Imperfect diagnostic testing reduces the power to detect significant predictors in classical cross-sectional studies. Assuming that the misclassification in diagnosis is random this can be dealt with by increasing the sample size of a study. However, the effects of imperfect tests in longitudinal data analyses are not as straightforward to anticipate, especially if the outcome of the test influences behaviour. The aim of this paper is to investigate the impact of imperfect test sensitivity on the determination of predictor variables in a longitudinal study.

Methodology/principal findings: To deal with imperfect test sensitivity affecting the response variable, we transformed the observed response variable into a set of possible temporal patterns of true disease status, whose prior probability was a function of the test sensitivity. We fitted a Bayesian discrete time survival model using an MCMC algorithm that treats the true response patterns as unknown parameters in the model. We applied our approach to epidemiological data of bovine tuberculosis outbreaks in England and investigated the effect of reduced test sensitivity in the determination of risk factors for the disease. We found that reduced test sensitivity led to changes to the collection of risk factors associated with the probability of an outbreak that were chosen in the 'best' model and to an increase in the uncertainty surrounding the parameter estimates for a model with a fixed set of risk factors that were associated with the response variable.

Conclusions/significance: We propose a novel algorithm to fit discrete survival models for longitudinal data where values of the response variable are uncertain. When analysing longitudinal data, uncertainty surrounding the response variable will affect the significance of the predictors and should therefore be accounted for either at the design stage by increasing the sample size or at the post analysis stage by conducting appropriate sensitivity analyses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Algorithms*
  • Animals
  • Bayes Theorem
  • Cattle
  • Diagnostic Errors / statistics & numerical data*
  • England / epidemiology
  • Longitudinal Studies / methods*
  • Models, Biological*
  • Risk Factors
  • Sensitivity and Specificity
  • Tuberculosis, Bovine / diagnosis*
  • Tuberculosis, Bovine / epidemiology*

Grants and funding

This work was funded by Defra (http:\\www.defra.gov.uk) under the Animal Health and Welfare call (project number SE3239). Defra had some input in the design of the initial field trial and in the collection and original analysis of the data. They did not actually have any input in the design and modelling/analysis of the data as presented in the paper. The authors provided with the data by AHVLA, came up with a new modelling approach (described in the paper), reformatting the data to the format required for the analysis, analysed and wrote the paper without any help by the funder. The authors sent Defra the draft manuscript prior to submission for comments as required by the term of their funding. The funders had no role in the data selection, preparation and analysis, decision to publish, or preparation of the manuscript.