Literature DB >> 31373355

Gamma models for estimating the odds ratio for a skewed biomarker measured in pools and subject to errors.

Dane R Van Domelen1, Emily M Mitchell2, Neil J Perkins3, Enrique F Schisterman3, Amita K Manatunga4, Yijian Huang4, Robert H Lyles4.   

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.
© The Author(s) 2019. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Keywords:  Biomarkers; Discriminant function; Gamma; Maximum likelihood; Measurement error; Pooling

Year:  2021        PMID: 31373355      PMCID: PMC8035988          DOI: 10.1093/biostatistics/kxz028

Source DB:  PubMed          Journal:  Biostatistics        ISSN: 1465-4644            Impact factor:   5.899


  15 in total

1.  Using pooled exposure assessment to improve efficiency in case-control studies.

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2.  The Collaborative Perinatal Project: lessons and legacy.

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4.  A Fresh Look at the Discriminant Function Approach for Estimating Crude or Adjusted Odds Ratios.

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Journal:  Am Stat       Date:  2009       Impact factor: 8.710

5.  Pooled exposure assessment for matched case-control studies.

Authors:  Paramita Saha-Chaudhuri; David M Umbach; Clarice R Weinberg
Journal:  Epidemiology       Date:  2011-09       Impact factor: 4.822

6.  Logistic regression with a continuous exposure measured in pools and subject to errors.

Authors:  Dane R Van Domelen; Emily M Mitchell; Neil J Perkins; Enrique F Schisterman; Amita K Manatunga; Yijian Huang; Robert H Lyles
Journal:  Stat Med       Date:  2018-07-18       Impact factor: 2.373

7.  An efficient design strategy for logistic regression using outcome- and covariate-dependent pooling of biospecimens prior to assay.

Authors:  Robert H Lyles; Emily M Mitchell; Clarice R Weinberg; David M Umbach; Enrique F Schisterman
Journal:  Biometrics       Date:  2016-03-09       Impact factor: 2.571

8.  Hybrid pooled-unpooled design for cost-efficient measurement of biomarkers.

Authors:  Enrique F Schisterman; Albert Vexler; Sunni L Mumford; Neil J Perkins
Journal:  Stat Med       Date:  2010-02-28       Impact factor: 2.373

9.  Circulating chemokine levels and miscarriage.

Authors:  Brian W Whitcomb; Enrique F Schisterman; Mark A Klebanoff; Mona Baumgarten; Alice Rhoton-Vlasak; Xiaoping Luo; Nasser Chegini
Journal:  Am J Epidemiol       Date:  2007-05-15       Impact factor: 4.897

10.  A Discriminant Function Approach to Adjust for Processing and Measurement Error When a Biomarker is Assayed in Pooled Samples.

Authors:  Robert H Lyles; Dane Van Domelen; Emily M Mitchell; Enrique F Schisterman
Journal:  Int J Environ Res Public Health       Date:  2015-11-18       Impact factor: 3.390

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