Literature DB >> 31299670

Estimating Outcome-Exposure Associations when Exposure Biomarker Detection Limits vary Across Batches.

Jonathan Boss1, Bhramar Mukherjee1,2, Kelly K Ferguson3, Amira Aker4, Akram N Alshawabkeh5, José F Cordero6, John D Meeker4, Sehee Kim1.   

Abstract

Limit of detection (LOD) issues are ubiquitous in exposure assessment. Although there is an extensive literature on modeling exposure data under such imperfect measurement processes, including likelihood-based methods and multiple imputation, the standard practice continues to be naïve single imputation by a constant (e.g., (Equation is included in full-text article.)). In this article, we consider the situation where, due to the practical logistics of data accrual, sampling, and resource constraints, exposure data are analyzed in multiple batches where the LOD and the proportion of censored observations differ across batches. Compounding this problem is the potential for nonrandom assignment of samples to each batch, often driven by enrollment patterns and biosample storage. This issue is particularly important for binary outcome data where batches may have different levels of outcome enrichment. We first consider variants of existing methods to address varying LODs across multiple batches. We then propose a likelihood-based multiple imputation strategy to impute observations that are below the LOD while simultaneously accounting for differential batch assignment. Our simulation study shows that our proposed method has superior estimation properties (i.e., bias, coverage, statistical efficiency) compared to standard alternatives, provided that distributional assumptions are satisfied. Additionally, in most batch assignment configurations, complete-case analysis can be made unbiased by including batch indicator terms in the analysis model, although this strategy is less efficient relative to the proposed method. We illustrate our method by analyzing data from a cohort study in Puerto Rico that is investigating the relation between endocrine disruptor exposures and preterm birth.

Entities:  

Year:  2019        PMID: 31299670      PMCID: PMC6677587          DOI: 10.1097/EDE.0000000000001052

Source DB:  PubMed          Journal:  Epidemiology        ISSN: 1044-3983            Impact factor:   4.822


  25 in total

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3.  The limitations due to exposure detection limits for regression models.

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Journal:  Neonatology       Date:  2008-12-02       Impact factor: 4.035

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Journal:  Int J Epidemiol       Date:  2009-08-10       Impact factor: 7.196

7.  Bifidobacterial supplementation reduces the incidence of necrotizing enterocolitis in a neonatal rat model.

Authors:  M S Caplan; R Miller-Catchpole; S Kaup; T Russell; M Lickerman; M Amer; Y Xiao; R Thomson
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Authors:  Francesca Dominici; Roger D Peng; Christopher D Barr; Michelle L Bell
Journal:  Epidemiology       Date:  2010-03       Impact factor: 4.822

9.  A distribution-based multiple imputation method for handling bivariate pesticide data with values below the limit of detection.

Authors:  Haiying Chen; Sara A Quandt; Joseph G Grzywacz; Thomas A Arcury
Journal:  Environ Health Perspect       Date:  2010-11-19       Impact factor: 9.031

10.  Epidemiologic evaluation of measurement data in the presence of detection limits.

Authors:  Jay H Lubin; Joanne S Colt; David Camann; Scott Davis; James R Cerhan; Richard K Severson; Leslie Bernstein; Patricia Hartge
Journal:  Environ Health Perspect       Date:  2004-12       Impact factor: 9.031

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2.  Gene regulation contributes to explain the impact of early life socioeconomic disadvantage on adult inflammatory levels in two cohort studies.

Authors:  Cristian Carmeli; Zoltán Kutalik; Pashupati P Mishra; Eleonora Porcu; Cyrille Delpierre; Olivier Delaneau; Michelle Kelly-Irving; Murielle Bochud; Nasser A Dhayat; Belen Ponte; Menno Pruijm; Georg Ehret; Mika Kähönen; Terho Lehtimäki; Olli T Raitakari; Paolo Vineis; Mika Kivimäki; Marc Chadeau-Hyam; Emmanouil Dermitzakis; Nicolas Vuilleumier; Silvia Stringhini
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