Literature DB >> 23038411

The robustness of generalized estimating equations for association tests in extended family data.

Bhoom Suktitipat1, Rasika A Mathias, Dhananjay Vaidya, Lisa R Yanek, J Hunter Young, Lewis C Becker, Diane M Becker, Alexander F Wilson, M Daniele Fallin.   

Abstract

Variance components analysis (VCA), the traditional method for handling correlations within families in genetic association studies, is computationally intensive for genome-wide analyses, and the computational burden of VCA increases with family size and the number of genetic markers. Alternative approaches that do not require the computation of familial correlations are preferable, provided that they do not inflate type I error or decrease power. We performed a simulation study to evaluate practical alternatives to VCA that use regression with generalized estimating equations (GEE) in extended family data. We compared the properties of linear regression with GEE applied to an entire extended family structure (GEE-EXT) and GEE applied to nuclear family structures split from these extended families (GEE-SPL) to variance components likelihood-based methods (FastAssoc). GEE-EXT was evaluated with and without robust variance estimators to estimate the standard errors. We observed similar average type I error rates from GEE-EXT and FastAssoc compared to GEE-SPL. Type I error rates for the GEE-EXT method with a robust variance estimator were marginally higher than the nominal rate when the minor allele frequency (MAF) was <0.1, but were close to the nominal rate when the MAF was ≥0.2. All methods gave consistent effect estimates and had similar power. In summary, the GEE framework with the robust variance estimator, the computationally fastest and least data management-intensive approach, appears to work well in extended families and thus provides a reasonable alternative to full variance components approaches for extended pedigrees in a genome-wide association study setting.
Copyright © 2012 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2012        PMID: 23038411      PMCID: PMC3736986          DOI: 10.1159/000341636

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  15 in total

1.  PBAT: tools for family-based association studies.

Authors:  Christoph Lange; Dawn DeMeo; Edwin K Silverman; Scott T Weiss; Nan M Laird
Journal:  Am J Hum Genet       Date:  2004-02       Impact factor: 11.025

2.  Genomewide rapid association using mixed model and regression: a fast and simple method for genomewide pedigree-based quantitative trait loci association analysis.

Authors:  Yurii S Aulchenko; Dirk-Jan de Koning; Chris Haley
Journal:  Genetics       Date:  2007-07-29       Impact factor: 4.562

3.  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

4.  The family based association test method: strategies for studying general genotype--phenotype associations.

Authors:  S Horvath; X Xu; N M Laird
Journal:  Eur J Hum Genet       Date:  2001-04       Impact factor: 4.246

5.  Longitudinal data analysis for discrete and continuous outcomes.

Authors:  S L Zeger; K Y Liang
Journal:  Biometrics       Date:  1986-03       Impact factor: 2.571

6.  Mixed linear model approach adapted for genome-wide association studies.

Authors:  Zhiwu Zhang; Elhan Ersoz; Chao-Qiang Lai; Rory J Todhunter; Hemant K Tiwari; Michael A Gore; Peter J Bradbury; Jianming Yu; Donna K Arnett; Jose M Ordovas; Edward S Buckler
Journal:  Nat Genet       Date:  2010-03-07       Impact factor: 38.330

7.  Incidence of coronary artery disease in siblings of patients with premature coronary artery disease: 10 years of follow-up.

Authors:  Dhananjay Vaidya; Lisa R Yanek; Taryn F Moy; Thomas A Pearson; Lewis C Becker; Diane M Becker
Journal:  Am J Cardiol       Date:  2007-08-16       Impact factor: 2.778

8.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

Authors:  R S Spielman; R E McGinnis; W J Ewens
Journal:  Am J Hum Genet       Date:  1993-03       Impact factor: 11.025

9.  The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study.

Authors:  Aldi T Kraja; Robert Culverhouse; E Warwick Daw; Jun Wu; Andrew Van Brunt; Michael A Province; Ingrid B Borecki
Journal:  BMC Proc       Date:  2009-12-15

10.  The Framingham Heart Study 100K SNP genome-wide association study resource: overview of 17 phenotype working group reports.

Authors:  L Adrienne Cupples; Heather T Arruda; Emelia J Benjamin; Ralph B D'Agostino; Serkalem Demissie; Anita L DeStefano; Josée Dupuis; Kathleen M Falls; Caroline S Fox; Daniel J Gottlieb; Diddahally R Govindaraju; Chao-Yu Guo; Nancy L Heard-Costa; Shih-Jen Hwang; Sekar Kathiresan; Douglas P Kiel; Jason M Laramie; Martin G Larson; Daniel Levy; Chun-Yu Liu; Kathryn L Lunetta; Matthew D Mailman; Alisa K Manning; James B Meigs; Joanne M Murabito; Christopher Newton-Cheh; George T O'Connor; Christopher J O'Donnell; Mona Pandey; Sudha Seshadri; Ramachandran S Vasan; Zhen Y Wang; Jemma B Wilk; Philip A Wolf; Qiong Yang; Larry D Atwood
Journal:  BMC Med Genet       Date:  2007       Impact factor: 2.103

View more
  5 in total

1.  Genome-wide gene-environment interactions on quantitative traits using family data.

Authors:  Colleen M Sitlani; Josée Dupuis; Kenneth M Rice; Fangui Sun; Achilleas N Pitsillides; L Adrienne Cupples; Bruce M Psaty
Journal:  Eur J Hum Genet       Date:  2015-12-02       Impact factor: 4.246

2.  Genome-wide association study of platelet aggregation in African Americans.

Authors:  Rehan Qayyum; Lewis C Becker; Diane M Becker; Nauder Faraday; Lisa R Yanek; Suzanne M Leal; Chad Shaw; Rasika Mathias; Bhoom Suktitipat; Paul F Bray
Journal:  BMC Genet       Date:  2015-05-30       Impact factor: 2.797

3.  Identification of rare variants for hypertension with incorporation of linkage information.

Authors:  Yen-Feng Chiu; Ren-Hua Chung; Chun-Yi Lee; Hui-Yi Kao; Lin Hou; Fang-Chi Hsu
Journal:  BMC Proc       Date:  2014-06-17

Review 4.  Benchmarking statistical methods for analyzing parent-child dyads in genetic association studies.

Authors:  Debashree Ray; Candelaria Vergara; Margaret A Taub; Genevieve Wojcik; Christine Ladd-Acosta; Terri H Beaty; Priya Duggal
Journal:  Genet Epidemiol       Date:  2022-04-22       Impact factor: 2.344

5.  Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation.

Authors:  Yoonhee Kim; Bhoom Suktitipat; Lisa R Yanek; Nauder Faraday; Alexander F Wilson; Diane M Becker; Lewis C Becker; Rasika A Mathias
Journal:  PLoS One       Date:  2013-05-21       Impact factor: 3.240

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.