Literature DB >> 1487139

Numerical comparisons of two formulations of the logistic regressive models with the mixed model in segregation analysis of discrete traits.

F M Demenais1, A E Laing, G E Bonney.   

Abstract

Segregation analysis of discrete traits can be conducted by the classical mixed model and the recently introduced regressive models. The mixed model assumes an underlying liability to the disease, to which a major gene, a multifactorial component, and random environment contribute independently. Affected persons have a liability exceeding a threshold. The regressive logistic models assume that the logarithm of the odds of being affected is a linear function of major genotype effects, the phenotypes of older relatives, and other covariates. A formulation of the regressive models, based on an underlying liability model, has been recently proposed. The regression coefficients on antecedents are expressed in terms of the relevant familial correlations and a one-to-one correspondence with the parameters of the mixed model can thus be established. Computer simulations are conducted to evaluate the fit of the two formulations of the regressive models to the mixed model on nuclear families. The two forms of the class D regressive model provide a good fit to a generated mixed model, in terms of both hypothesis testing and parameter estimation. The simpler class A regressive model, which assumes that the outcomes of children depend solely on the outcomes of parents, is not robust against a sib-sib correlation exceeding that specified by the model, emphasizing testing class A against class D. The studies reported here show that if the true state of nature is that described by the mixed model, then a regressive model will do just as well. Moreover, the regressive models, allowing for more patterns of family dependence, provide a flexible framework to understand gene-environment interactions in complex diseases.

Entities:  

Mesh:

Year:  1992        PMID: 1487139     DOI: 10.1002/gepi.1370090605

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  6 in total

1.  Interactions between genetic and reproductive factors in breast cancer risk in a French family sample.

Authors:  N Andrieu; F Demenais
Journal:  Am J Hum Genet       Date:  1997-09       Impact factor: 11.025

2.  An autologistic model for the genetic analysis of familial binary data.

Authors:  L Abel; J L Golmard; A Mallet
Journal:  Am J Hum Genet       Date:  1993-10       Impact factor: 11.025

3.  Evidence for a major gene controlling susceptibility to tegumentary leishmaniasis in a recently exposed Bolivian population.

Authors:  A Alcaïs; L Abel; C David; M E Torrez; P Flandre; J P Dedet
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

4.  Multiple etiologies for Alzheimer disease are revealed by segregation analysis.

Authors:  V S Rao; C M van Duijn; L Connor-Lacke; L A Cupples; J H Growdon; L A Farrer
Journal:  Am J Hum Genet       Date:  1994-11       Impact factor: 11.025

5.  Segregation and linkage analysis of serum angiotensin I-converting enzyme levels: evidence for two quantitative-trait loci.

Authors:  C A McKenzie; C Julier; T Forrester; N McFarlane-Anderson; B Keavney; G M Lathrop; P J Ratcliffe; M Farrall
Journal:  Am J Hum Genet       Date:  1995-12       Impact factor: 11.025

6.  A genome-wide search replicates evidence of a quantitative trait locus for circulating angiotensin I-converting enzyme (ACE) unlinked to the ACE gene.

Authors:  Colin A McKenzie; Xiaofeng Zhu; Terrence E Forrester; Amy Luke; Adebowale A Adeyemo; Nourdine Bouzekri; Richard S Cooper
Journal:  BMC Med Genomics       Date:  2008-06-10       Impact factor: 3.063

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.