Literature DB >> 10053023

A parametric copula model for analysis of familial binary data.

D A Trégou t1, P Ducimetière, V Bocquet, S Visvikis, F Soubrier, L Tiret.   

Abstract

Modeling the joint distribution of a binary trait (disease) within families is a tedious challenge, owing to the lack of a general statistical model with desirable properties such as the multivariate Gaussian model for a quantitative trait. Models have been proposed that either assume the existence of an underlying liability variable, the reality of which cannot be checked, or provide estimates of aggregation parameters that are dependent on the ordering of family members and on family size. We describe how a class of copula models for the analysis of exchangeable categorical data can be incorporated into a familial framework. In this class of models, the joint distribution of binary outcomes is characterized by a function of the given marginals. This function, referred to as a "copula," depends on an aggregation parameter that is weakly dependent on the marginal distributions. We propose to decompose a nuclear family into two sets of equicorrelated data (parents and offspring), each of which is characterized by an aggregation parameter (alphaFM and alphaSS, respectively). The marginal probabilities are modeled through a logistic representation. The advantage of this model is that it provides estimates of the aggregation parameters that are independent of family size and does not require any arbitrary ordering of sibs. It can be incorporated easily into segregation or combined segregation-linkage analysis and does not require extensive computer time. As an illustration, we applied this model to a combined segregation-linkage analysis of levels of plasma angiotensin I-converting enzyme (ACE) dichotomized into two classes according to the median. The conclusions of this analysis were very similar to those we had reported in an earlier familial analysis of quantitative ACE levels.

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Year:  1999        PMID: 10053023      PMCID: PMC1377806          DOI: 10.1086/302279

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  16 in total

1.  Logistic regression for clustered binary data in proband studies with application to familial aggregation of sleep disorders.

Authors:  T D Tosteson; B Rosner; S Redline
Journal:  Biometrics       Date:  1991-12       Impact factor: 2.571

2.  Measuring familial aggregation by using odds-ratio regression models.

Authors:  K Y Liang; T H Beaty
Journal:  Genet Epidemiol       Date:  1991       Impact factor: 2.135

3.  Regressive logistic models for familial diseases: a formulation assuming an underlying liability model.

Authors:  F M Demenais
Journal:  Am J Hum Genet       Date:  1991-10       Impact factor: 11.025

4.  Testing association between candidate-gene markers and phenotype in related individuals, by use of estimating equations.

Authors:  D A Trégouët; P Ducimetière; L Tiret
Journal:  Am J Hum Genet       Date:  1997-07       Impact factor: 11.025

5.  Sampling considerations in the gathering and analysis of pedigree data.

Authors:  R C Elston; E Sobel
Journal:  Am J Hum Genet       Date:  1979-01       Impact factor: 11.025

6.  Analysis of family resemblance. 3. Complex segregation of quantitative traits.

Authors:  N E Morton; C J MacLean
Journal:  Am J Hum Genet       Date:  1974-07       Impact factor: 11.025

7.  Regressive logistic models for familial disease and other binary traits.

Authors:  G E Bonney
Journal:  Biometrics       Date:  1986-09       Impact factor: 2.571

8.  A unified model for complex segregation analysis.

Authors:  J M Lalouel; D C Rao; N E Morton; R C Elston
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

9.  A time-dependent logistic hazard function for modeling variable age of onset in analysis of familial diseases.

Authors:  L Abel; G E Bonney
Journal:  Genet Epidemiol       Date:  1990       Impact factor: 2.135

10.  Evidence, from combined segregation and linkage analysis, that a variant of the angiotensin I-converting enzyme (ACE) gene controls plasma ACE levels.

Authors:  L Tiret; B Rigat; S Visvikis; C Breda; P Corvol; F Cambien; F Soubrier
Journal:  Am J Hum Genet       Date:  1992-07       Impact factor: 11.025

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  2 in total

1.  Quantitative trait linkage analysis using Gaussian copulas.

Authors:  Mingyao Li; Michael Boehnke; Gonçalo R Abecasis; Peter X-K Song
Journal:  Genetics       Date:  2006-06-04       Impact factor: 4.562

2.  Copula miss-specification in REML multivariate genetic animal model estimation.

Authors:  Tom Rohmer; Anne Ricard; Ingrid David
Journal:  Genet Sel Evol       Date:  2022-05-26       Impact factor: 5.100

  2 in total

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