Literature DB >> 20357904

A Novel Application of a Bivariate Regression Model for Binary and Continuous Outcomes to Studies of Fetal Toxicity.

Julie S Najita1, Yi Li, Paul J Catalano.   

Abstract

Public health concerns over the occurrence of birth defects and developmental abnormalities that may occur as a result of prenatal exposure to drugs, chemicals, and other environmental factors has led to an increasing number of developmental toxicity studies. Because fetal pups are commonly evaluated for multiple outcomes, data analysis frequently involves a joint modeling approach. In this paper, we focus on modelling clustered binary and continuous outcomes in the setting where both outcomes are potentially observable in all offspring but, due to practical limitations, the continuous outcome is only observed in a subset of offspring. The subset is not a simple random sample (SRS) but is selected by the experimenter under a prespecified probability model.While joint models for binary and continuous outcomes have been developed when both outcomes are available for every fetus, many existing approaches are not directly applicable when the continuous outcome is not observed in a SRS. We adapt a likelihood-based approach for jointly modelling clustered binary and continuous outcomes when the continuous response is missing by design and missingness depends on the binary trait. The approach takes into account the probability that a fetus is selected in the subset. Through the use of a partial likelihood, valid estimates can be obtained by a simple modification to the partial likelihood score. Data involving the herbicide 2,4,5-T are analyzed. Simulation results confirm the approach.

Entities:  

Year:  2009        PMID: 20357904      PMCID: PMC2847301          DOI: 10.1111/j.1467-9876.2009.00667.x

Source DB:  PubMed          Journal:  J R Stat Soc Ser C Appl Stat        ISSN: 0035-9254            Impact factor:   1.864


  16 in total

1.  Regression models and risk estimation for mixed discrete and continuous outcomes in developmental toxicology.

Authors:  M M Regan; P J Catalano
Journal:  Risk Anal       Date:  2000-06       Impact factor: 4.000

2.  Relationship between fetal weight and litter size in rats: application to reproductive toxicology studies.

Authors:  A Romero; F Villamayor; M T Grau; A Sacristán; J A Ortiz
Journal:  Reprod Toxicol       Date:  1992       Impact factor: 3.143

3.  Comments about Joint Modeling of Cluster Size and Binary and Continuous Subunit-Specific Outcomes.

Authors:  Ralitza V Gueorguieva
Journal:  Biometrics       Date:  2005-09       Impact factor: 2.571

4.  Quantitative risk assessment for developmental toxicity.

Authors:  L Ryan
Journal:  Biometrics       Date:  1992-03       Impact factor: 2.571

5.  Ocular changes in the mouse embryo following acute maternal ethanol intoxication.

Authors:  L A Kennedy; M J Elliott
Journal:  Int J Dev Neurosci       Date:  1986       Impact factor: 2.457

6.  Likelihood models for clustered binary and continuous outcomes: application to developmental toxicology.

Authors:  M M Regan; P J Catalano
Journal:  Biometrics       Date:  1999-09       Impact factor: 2.571

7.  Statistical model for fetal death, fetal weight, and malformation in developmental toxicity studies.

Authors:  P J Catalano; D O Scharfstein; L M Ryan; C A Kimmel; G L Kimmel
Journal:  Teratology       Date:  1993-04

8.  Effects of prenatal perfluorooctane sulfonate (PFOS) exposure on lung maturation in the perinatal rat.

Authors:  R C Grasty; J A Bjork; K B Wallace; D C Wolf; C S Lau; J M Rogers
Journal:  Birth Defects Res B Dev Reprod Toxicol       Date:  2005-10

9.  A malformation incidence dose-response model incorporating fetal weight and/or litter size as covariates.

Authors:  J Chen
Journal:  Risk Anal       Date:  1993-10       Impact factor: 4.000

10.  A Bayesian approach for joint modeling of cluster size and subunit-specific outcomes.

Authors:  David B Dunson; Zhen Chen; Jean Harry
Journal:  Biometrics       Date:  2003-09       Impact factor: 2.571

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  2 in total

1.  On determining the BMD from multiple outcomes in developmental toxicity studies when one outcome is intentionally missing.

Authors:  Julie S Najita; Paul J Catalano
Journal:  Risk Anal       Date:  2012-12-12       Impact factor: 4.000

2.  Secondary phenotype analysis in ascertained family designs: application to the Leiden longevity study.

Authors:  Renaud Tissier; Roula Tsonaka; Simon P Mooijaart; Eline Slagboom; Jeanine J Houwing-Duistermaat
Journal:  Stat Med       Date:  2017-03-16       Impact factor: 2.373

  2 in total

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