Literature DB >> 18650222

Making the most of case-mother/control-mother studies.

M Shi1, D M Umbach, S H Vermeulen, C R Weinberg.   

Abstract

The prenatal environment plays an important role in many conditions, particularly those with onset early in life, such as childhood cancers and birth defects. Because both maternal and fetal genotypes can influence risk, investigators sometimes use a case-mother/control-mother design, with mother-offspring pairs as the unit of analysis, to study genetic factors. Risk models should account for both the maternal genotype and the correlated fetal genotype to avoid confounding. The usual logistic regression analysis, however, fails to fully exploit the fact that these are mothers and offspring. Consider an autosomal, diallelic locus, which could be related to disease susceptibility either directly or through linkage with a polymorphic causal locus. Three nested levels of assumptions are often natural and plausible. The first level simply assumes Mendelian inheritance. The second further assumes parental mating symmetry for the studied locus in the source population. The third additionally assumes parental allelic exchangeability. Those assumptions imply certain nonlinear constraints; the authors enforce those constraints by using Poisson regression together with the expectation-maximization algorithm. Calculations reveal that improvements in efficiency over the usual logistic analysis can be substantial, even if only the Mendelian assumption is honored. Benefits are even more marked if, as is typical, information on genotype is missing for some individuals.

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Year:  2008        PMID: 18650222      PMCID: PMC2732952          DOI: 10.1093/aje/kwn149

Source DB:  PubMed          Journal:  Am J Epidemiol        ISSN: 0002-9262            Impact factor:   4.897


  8 in total

1.  Testing for linkage disequilibrium, maternal effects, and imprinting with (In)complete case-parent triads, by use of the computer program LEM.

Authors:  E J van Den Oord; J K Vermunt
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  The use of case-parent triads to study joint effects of genotype and exposure.

Authors:  D M Umbach; C R Weinberg
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

3.  Population stratification in epidemiologic studies of common genetic variants and cancer: quantification of bias.

Authors:  S Wacholder; N Rothman; N Caporaso
Journal:  J Natl Cancer Inst       Date:  2000-07-19       Impact factor: 13.506

4.  Exploiting gene-environment independence in family-based case-control studies: increased power for detecting associations, interactions and joint effects.

Authors:  Nilanjan Chatterjee; Zeynep Kalaylioglu; Raymond J Carroll
Journal:  Genet Epidemiol       Date:  2005-02       Impact factor: 2.135

5.  Identification of risk-related haplotypes with the use of multiple SNPs from nuclear families.

Authors:  Min Shi; David M Umbach; Clarice R Weinberg
Journal:  Am J Hum Genet       Date:  2007-05-15       Impact factor: 11.025

6.  Distinguishing the effects of maternal and offspring genes through studies of "case-parent triads".

Authors:  A J Wilcox; C R Weinberg; R T Lie
Journal:  Am J Epidemiol       Date:  1998-11-01       Impact factor: 4.897

7.  A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.

Authors:  C R Weinberg; A J Wilcox; R T Lie
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

8.  Is mutated MTHFR a risk factor for neural tube defects?

Authors:  D L Posey; M J Khoury; J Mulinare; M J Adams; C Y Ou
Journal:  Lancet       Date:  1996-03-09       Impact factor: 79.321

  8 in total
  21 in total

1.  Analysis of case-parent trios for imprinting effect using a loglinear model with adjustment for sex-of-parent-specific transmission ratio distortion.

Authors:  Lam Opal Huang; Claire Infante-Rivard; Aurélie Labbe
Journal:  Hum Genet       Date:  2017-06-19       Impact factor: 4.132

2.  Using cases and parents to study multiplicative gene-by-environment interaction.

Authors:  Emily O Kistner; Min Shi; Clarice R Weinberg
Journal:  Am J Epidemiol       Date:  2009-05-29       Impact factor: 4.897

3.  The genetics of preterm birth: using what we know to design better association studies.

Authors:  Clarice R Weinberg; Min Shi
Journal:  Am J Epidemiol       Date:  2009-10-23       Impact factor: 4.897

4.  A fetal variant in the GCM1 gene is associated with pregnancy induced hypertension in a predominantly hispanic population.

Authors:  Melissa L Wilson; Doerthe Brueggmann; Daniel H Desmond; John E Mandeville; T Murphy Goodwin; Sue Ann Ingles
Journal:  Int J Mol Epidemiol Genet       Date:  2011-05-05

5.  Disinfection by-products exposure and intra-uterine growth restriction: Do genetic polymorphisms of CYP2E1or deletion of GSTM1 or GSTT1 modify the association?

Authors:  Patrick Levallois; Yves Giguère; Molière Nguile-Makao; Manuel Rodriguez; Céline Campagna; Robert Tardif; Alexandre Bureau
Journal:  Environ Int       Date:  2016-04-22       Impact factor: 9.621

6.  Prenatal exposure to drinking-water chlorination by-products, cytochrome P450 gene polymorphisms and small-for-gestational-age neonates.

Authors:  Samuella G Bonou; Patrick Levallois; Yves Giguère; Manuel Rodriguez; Alexandre Bureau
Journal:  Reprod Toxicol       Date:  2017-07-31       Impact factor: 3.143

7.  Case-sibling studies that acknowledge unstudied parents and permit the inclusion of unmatched individuals.

Authors:  Min Shi; David M Umbach; Clarice R Weinberg
Journal:  Int J Epidemiol       Date:  2012-12-17       Impact factor: 7.196

8.  Joint detection of association, imprinting and maternal effects using all children and their parents.

Authors:  Miao Han; Yue-Qing Hu; Shili Lin
Journal:  Eur J Hum Genet       Date:  2013-03-27       Impact factor: 4.246

9.  Detecting maternal-fetal genotype interactions associated with conotruncal heart defects: a haplotype-based analysis with penalized logistic regression.

Authors:  Ming Li; Stephen W Erickson; Charlotte A Hobbs; Jingyun Li; Xinyu Tang; Todd G Nick; Stewart L Macleod; Mario A Cleves
Journal:  Genet Epidemiol       Date:  2014-03-02       Impact factor: 2.135

10.  Detection of fetomaternal genotype associations in early-onset disorders: evaluation of different methods and their application to childhood leukemia.

Authors:  Jasmine Healy; Mathieu Bourgey; Chantal Richer; Daniel Sinnett; Marie-Helene Roy-Gagnon
Journal:  J Biomed Biotechnol       Date:  2010-06-09
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