Literature DB >> 23248214

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

Min Shi1, David M Umbach, Clarice R Weinberg.   

Abstract

BACKGROUND: Family-based designs enable assessment of genetic associations without bias from population stratification. When parents are not readily available - especially for diseases with onset later in life - the case-sibling design, where each case is matched with one or more unaffected siblings, is useful. Analysis typically accounts for within-family dependencies by using conditional logistic regression (CLR).
METHODS: We consider an alternative to CLR that treats each case-sibling set as a nuclear family with both parents missing by design. One can carry out maximum likelihood analysis by using the Expectation-Maximization (EM) algorithm to account for missing parental genotypes. We compare conditional logistic regression and the missing-parents approach under several risk scenarios.
RESULTS: We show that the missing-parents approach improves power when some families have more than one unaffected sibling and that under weak assumptions the approach permits the incorporation of supplemental cases who have no sibling available and supplemental controls whose case sibling is unavailable (e.g., due to disability or death).
CONCLUSION: The missing-parents approach offers both improved statistical efficiency and asymptotically unbiased estimation for genotype relative risks and genotype-by-exposure interaction parameters.

Entities:  

Mesh:

Year:  2012        PMID: 23248214      PMCID: PMC3600623          DOI: 10.1093/ije/dys212

Source DB:  PubMed          Journal:  Int J Epidemiol        ISSN: 0300-5771            Impact factor:   7.196


  29 in total

1.  Application of the missing-indicator method in matched case-control studies with incomplete data.

Authors:  M Huberman; B Langholz
Journal:  Am J Epidemiol       Date:  1999-12-15       Impact factor: 4.897

2.  Testing linkage disequilibrium in sibships.

Authors:  K D Siegmund; B Langholz; P Kraft; D C Thomas
Journal:  Am J Hum Genet       Date:  2000-05-30       Impact factor: 11.025

3.  A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information.

Authors:  D Rabinowitz; N Laird
Journal:  Hum Hered       Date:  2000 Jul-Aug       Impact factor: 0.444

4.  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

5.  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

6.  Efficient use of siblings in testing for linkage and association.

Authors:  R H Rieger; N L Kaplan; C R Weinberg
Journal:  Genet Epidemiol       Date:  2001-02       Impact factor: 2.135

7.  On the use of population attributable fraction to determine sample size for case-control studies of gene-environment interaction.

Authors:  Quanhe Yang; Muin J Khoury; J M Friedman; W Dana Flanders
Journal:  Epidemiology       Date:  2003-03       Impact factor: 4.822

8.  Power evaluations for family-based tests of association with incomplete parental genotypes.

Authors:  Qiong Yang; Xin Xu; Nan Laird
Journal:  Genetics       Date:  2003-05       Impact factor: 4.562

9.  Accounting for linkage in family-based tests of association with missing parental genotypes.

Authors:  Eden R Martin; Meredyth P Bass; Elizabeth R Hauser; Norman L Kaplan
Journal:  Am J Hum Genet       Date:  2003-10-09       Impact factor: 11.025

10.  Properties of case/pseudocontrol analysis for genetic association studies: Effects of recombination, ascertainment, and multiple affected offspring.

Authors:  Heather J Cordell
Journal:  Genet Epidemiol       Date:  2004-04       Impact factor: 2.135

View more
  2 in total

1.  Previous GWAS hits in relation to young-onset breast cancer.

Authors:  Min Shi; Katie M O'Brien; Dale P Sandler; Jack A Taylor; Dmitri V Zaykin; Clarice R Weinberg
Journal:  Breast Cancer Res Treat       Date:  2016-11-15       Impact factor: 4.872

2.  A family-based, genome-wide association study of young-onset breast cancer: inherited variants and maternally mediated effects.

Authors:  Katie M O'Brien; Min Shi; Dale P Sandler; Jack A Taylor; Dmitri V Zaykin; Jean Keller; Alison S Wise; Clarice R Weinberg
Journal:  Eur J Hum Genet       Date:  2016-02-17       Impact factor: 4.246

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.