Literature DB >> 34556968

AN EM COMPOSITE LIKELIHOOD APPROACH FOR MULTISTAGE SAMPLING OF FAMILY DATA.

Y Choi1,2, L Briollais2,3.   

Abstract

Multistage sampling of family data is a common design in the field of genetic epidemiology, but appropriate methodologies for analyzing data collected under this design are still lacking. We propose here a statistical approach based on the composite likelihood framework. The composite likelihood is a weighted product of individual likelihoods corresponding to the sampling strata, where the weights are the inverse sampling probabilities of the families in each stratum. Our approach is developed for time-to-event data and can handle missing genetic covariates by using an Expectation-Maximization algorithm. A robust variance estimator is employed to account for the dependence of individuals within families. Our simulation studies have demonstrated the good properties of our approach in terms of consistency and efficiency of the genetic relative risk estimate in the presence of missing genotypes and under different multistage sampling designs. Finally, an application to a familial study of early-onset breast cancer shows the interest of our approach. While it confirms the important effect of the genes BRCA1 and BRCA2 in these families, it also shows that incorrect inference can be made about this effect if the sampling design is not properly taken into account.

Entities:  

Keywords:  Composite likelihood; EM algorithm; family data; missing genotype; multistage sampling

Year:  2011        PMID: 34556968      PMCID: PMC8457513     

Source DB:  PubMed          Journal:  Stat Sin        ISSN: 1017-0405            Impact factor:   1.330


  9 in total

1.  Multistage sampling for disease family registries.

Authors:  K D Siegmund; A S Whittemore; D C Thomas
Journal:  J Natl Cancer Inst Monogr       Date:  1999

2.  Composite likelihood and two-stage estimation in family studies.

Authors:  Elisabeth Wreford Andersen
Journal:  Biostatistics       Date:  2004-01       Impact factor: 5.899

3.  Two-stage estimation in copula models used in family studies.

Authors:  Elisabeth Wreford Andersen
Journal:  Lifetime Data Anal       Date:  2005-09       Impact factor: 1.588

4.  Estimating disease risk associated with mutated genes in family-based designs.

Authors:  Yun-Hee Choi; Karen A Kopciuk; Laurent Briollais
Journal:  Hum Hered       Date:  2008-07-09       Impact factor: 0.444

5.  Multi-stage sampling in genetic epidemiology.

Authors:  A S Whittemore; J Halpern
Journal:  Stat Med       Date:  1997 Jan 15-Feb 15       Impact factor: 2.373

6.  Likelihood analysis of multi-state models for disease incidence and mortality.

Authors:  J D Kalbfleisch; J F Lawless
Journal:  Stat Med       Date:  1988 Jan-Feb       Impact factor: 2.373

Review 7.  Common genetic variants and cancer risk in Mendelian cancer syndromes.

Authors:  Antonis C Antoniou; Georgia Chenevix-Trench
Journal:  Curr Opin Genet Dev       Date:  2010-06       Impact factor: 5.578

8.  On the use of familial aggregation in population-based case probands for calculating penetrance.

Authors:  Colin B Begg
Journal:  J Natl Cancer Inst       Date:  2002-08-21       Impact factor: 13.506

9.  The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer.

Authors:  Esther M John; John L Hopper; Jeanne C Beck; Julia A Knight; Susan L Neuhausen; Ruby T Senie; Argyrios Ziogas; Irene L Andrulis; Hoda Anton-Culver; Norman Boyd; Saundra S Buys; Mary B Daly; Frances P O'Malley; Regina M Santella; Melissa C Southey; Vickie L Venne; Deon J Venter; Dee W West; Alice S Whittemore; Daniela Seminara
Journal:  Breast Cancer Res       Date:  2004-05-19       Impact factor: 6.466

  9 in total

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