ArticleStatistics in medicine2012
Assessment of skewed exposure in case-control studies with pooling.
Article in Statistics in medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
10 citing papers in PubMed.
- Gamma models for estimating the odds ratio for a skewed biomarker measured in pools and subject to errors.Biostatistics (Oxford, England) · 2021Article
- Exposure to Persistent Organic Pollutants and Birth Characteristics: The Upstate KIDS Study.Epidemiology (Cambridge, Mass.) · 2019Article
- Estimating relative risk of a log-transformed exposure measured in pools.Statistics in medicine · 2016Article
- Case-control data analysis for randomly pooled biomarkers.Biometrical journal. Biometrische Zeitschrift · 2016Article
- Estimation of interaction effects using pooled biospecimens in a case-control study.Statistics in medicine · 2016Article
- Pooling Bio-Specimens in the Presence of Measurement Error and Non-Linearity in Dose-Response: Simulation Study in the Context of a Birth Cohort Investigating Risk Factors for Autism Spectrum Disorders.International journal of environmental research and public health · 2015Article
- Positing, fitting, and selecting regression models for pooled biomarker data.Statistics in medicine · 2015Article
- Semiparametric regression models for a right-skewed outcome subject to pooling.American journal of epidemiology · 2015Article
- Regression for skewed biomarker outcomes subject to pooling.Biometrics · 2014Article
- The biomarker revolution.Statistics in medicine · 2012Article
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5 authors.
Funding
Abstract
Pooling-based strategies that combine samples from multiple participants for laboratory assays have been proposed for epidemiologic investigations of biomarkers to address issues including cost, efficiency, detection, and when minimal sample volume is available. A modification of the standard logistic regression model has been previously described to allow use with pooled data; however, this model makes assumptions regarding exposure distribution and logit-linearity of risk (i.e., constant odds ratio) that can be violated in practice. We were motivated by a nested case-control study of miscarriage and inflammatory factors with highly skewed distributions to develop a more flexible model for analysis of pooled data. Using characteristics of the gamma distribution and the relation between models of binary outcome conditional on exposure and of exposure conditional on outcome, we use a modified logistic regression to accommodate nonlinearity because of unequal shape parameters in gamma distributed exposure for cases and controls. Using simulations, we compare our approach with existing methods for logistic regression for pooled data considering: (1) constant and dose-dependent effects; (2) gamma and log-normal distributed exposure; (3) effect size; and (4) the proportions of biospecimens pooled. We show that our approach allows estimation of odds ratios that vary with exposure level, yet has minimal loss of efficiency compared with existing approaches when exposure effects are dose-invariant. Our model performed similarly to a maximum likelihood estimation approach in terms of bias and efficiency, and provides an easily implemented approach for estimation with pooled biomarker data when effects may not be constant across exposure.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.