The objective of this application is to continue developing improved methods of analysis of disease incidence data in family studies. Issues to be addressed include censored age-at-onset outcomes, major genes, polygenes, and shared unmeasured environmental factors, linkage to multiple polymorphic markers, and associations with candidate genes, genetic heterogeneity, measured environmental exposures with gene-environment interactions, misclassified or missing data, and correction for ascertainment. The basic model being considered is an extension of the proportional hazards model which includes latent variables for each individual representing their unobserved genotypes. A Monte Carlo technique, known as Gibbs sampling, and generalized estimating equations (GEE) methods are used to overcome the considerable computational burden that would otherwise be required in a full likelihood treatment.
The specific aims of this application have been extended beyond those of the original application. The investigators have omitted the previous aim for development of computer software and have added two aims.
The specific aims i nclude 1) further development of the methods, with priority given to extensions to multi-locus mapping, genetic heterogeneity, ascertainment correction, and Markov chain Monte Carlo theory; 2) further development of the generalized estimating equations approach to segregation analysis extending it to analysis of binary and survival data, and to ascertainment through probands; 3) exploration of statistical design issues in family studies aimed to segregation, linkage, candidate gene, and gene environment interaction analyses; 4) simulation studies of the performance of the methods compared with currently available methods in genetics and epidemiology, including assessment of the power to distinguish alternative genetic models and patterns of gene environment interactions, the robustness of the methods to misclassification of the model or the ascertainment protocol, and the relative efficiency of alternative designs; and 5) applications to various family studies the investigators are conducting, including breast and ovarian cancer, colorectal cancer, and diabetes.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
2R01CA052862-04A1
Application #
2095038
Study Section
Nutrition Study Section (NTN)
Project Start
1991-04-01
Project End
1998-02-28
Budget Start
1995-03-10
Budget End
1996-02-29
Support Year
4
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Southern California
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Schmit, Stephanie L; Figueiredo, Jane C; Cortessis, Victoria K et al. (2015) The Influence of Screening for Precancerous Lesions on Family-Based Genetic Association Tests: An Example of Colorectal Polyps and Cancer. Am J Epidemiol 182:714-22
Choong, Eva; Quteineh, Lina; Cardinaux, Jean-René et al. (2013) Influence of CRTC1 polymorphisms on body mass index and fat mass in psychiatric patients and the general adult population. JAMA Psychiatry 70:1011-9
Tzeng, Jung-Ying; Zhang, Daowen; Chang, Sheng-Mao et al. (2009) Gene-trait similarity regression for multimarker-based association analysis. Biometrics 65:822-32
Kerber, Richard A; Amos, Christopher I; Yeap, Beow Y et al. (2008) Design considerations in a sib-pair study of linkage for susceptibility loci in cancer. BMC Med Genet 9:64
Thomas, Duncan C (2007) Multistage sampling for latent variable models. Lifetime Data Anal 13:565-81
Thomas, Duncan C (2007) Viewpoint: using gene-environment interactions to dissect the effects of complex mixtures. J Expo Sci Environ Epidemiol 17 Suppl 2:S71-4
Lewinger, Juan Pablo; Conti, David V; Baurley, James W et al. (2007) Hierarchical Bayes prioritization of marker associations from a genome-wide association scan for further investigation. Genet Epidemiol 31:871-82
Gauderman, W James; Murcray, Cassandra; Gilliland, Frank et al. (2007) Testing association between disease and multiple SNPs in a candidate gene. Genet Epidemiol 31:383-95
Kraft, Peter; Yen, Yu-Chun; Stram, Daniel O et al. (2007) Exploiting gene-environment interaction to detect genetic associations. Hum Hered 63:111-9
Millstein, Joshua; Siegmund, Kimberly D; Conti, David V et al. (2005) Identifying susceptibility genes by using joint tests of association and linkage and accounting for epistasis. BMC Genet 6 Suppl 1:S147

Showing the most recent 10 out of 63 publications