Comparison of models for analyzing two-group, cross-sectional data with a Gaussian outcome subject to a detection limit

Stat Methods Med Res. 2016 Dec;25(6):2733-2749. doi: 10.1177/0962280214531684. Epub 2014 May 5.

Abstract

A potential difficulty in the analysis of biomarker data occurs when data are subject to a detection limit. This detection limit is often defined as the point at which the true values cannot be measured reliably. Multiple, regression-type models designed to analyze such data exist. Studies have compared the bias among such models, but few have compared their statistical power. This simulation study provides a comparison of approaches for analyzing two-group, cross-sectional data with a Gaussian-distributed outcome by exploring statistical power and effect size confidence interval coverage of four models able to be implemented in standard software. We found using a Tobit model fit by maximum likelihood provides the best power and coverage. An example using human immunodeficiency virus type 1 ribonucleic acid data is used to illustrate the inferential differences in these models.

Keywords: limit of detection; regression; statistical power.

Publication types

  • Comparative Study

MeSH terms

  • Anti-HIV Agents / therapeutic use
  • Bias
  • Cross-Sectional Studies / methods*
  • HIV Infections / drug therapy
  • HIV Infections / virology
  • HIV-1 / drug effects
  • HIV-1 / genetics*
  • HIV-1 / isolation & purification*
  • Humans
  • Likelihood Functions
  • Limit of Detection*
  • Multivariate Analysis
  • Normal Distribution*
  • Probability
  • RNA, Viral / analysis
  • RNA, Viral / genetics
  • Raltegravir Potassium / therapeutic use
  • Software
  • Viral Load / drug effects

Substances

  • Anti-HIV Agents
  • RNA, Viral
  • Raltegravir Potassium