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Gamma models for estimating the odds ratio for a skewed biomarker measured in pools and subject to errors.
Van Domelen, Dane R; Mitchell, Emily M; Perkins, Neil J; Schisterman, Enrique F; Manatunga, Amita K; Huang, Yijian; Lyles, Robert H.
  • Van Domelen DR; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, 1518 Clifton Rd., Atlanta, GA, USA.
  • Mitchell EM; Center for Financing, Access, and Cost Trends, Agency for Healthcare Research and Quality, 5600 Fishers Lane, Rockville, MD, USA.
  • Perkins NJ; Eunice Kennedy Shriver National Institute of Child Health and Human Development, Epidemiology Branch, Division of Intramural Population Health Research, 6710B Rockledge Drive, Bethesda, MD, USA.
  • Schisterman EF; Eunice Kennedy Shriver National Institute of Child Health and Human Development, Epidemiology Branch, Division of Intramural Population Health Research, 6710B Rockledge Drive, Bethesda, MD, USA.
  • Manatunga AK; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, 1518 Clifton Rd., Atlanta, GA 30322, USA.
  • Huang Y; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, 1518 Clifton Rd., Atlanta, GA 30322, USA.
  • Lyles RH; Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, 1518 Clifton Rd., Atlanta, GA 30322, USA.
Biostatistics ; 22(2): 250-265, 2021 04 10.
Article en En | MEDLINE | ID: mdl-31373355
ABSTRACT
Measuring a biomarker in pooled samples from multiple cases or controls can lead to cost-effective estimation of a covariate-adjusted odds ratio, particularly for expensive assays. But pooled measurements may be affected by assay-related measurement error (ME) and/or pooling-related processing error (PE), which can induce bias if ignored. Building on recently developed methods for a normal biomarker subject to additive errors, we present two related estimators for a right-skewed biomarker subject to multiplicative errors one based on logistic regression and the other based on a Gamma discriminant function model. Applied to a reproductive health dataset with a right-skewed cytokine measured in pools of size 1 and 2, both methods suggest no association with spontaneous abortion. The fitted models indicate little ME but fairly severe PE, the latter of which is much too large to ignore. Simulations mimicking these data with a non-unity odds ratio confirm validity of the estimators and illustrate how PE can detract from pooling-related gains in statistical efficiency. These methods address a key issue associated with the homogeneous pools study design and should facilitate valid odds ratio estimation at a lower cost in a wide range of scenarios.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proyectos de Investigación Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Año: 2021 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proyectos de Investigación Tipo de estudio: Etiology_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Pregnancy Idioma: En Año: 2021 Tipo del documento: Article