Quantitative trait locus analysis of longitudinal quantitative trait data in complex pedigrees

被引:27
作者
Macgregor, S
Knott, SA
White, I
Visscher, PM
机构
[1] Cardiff Univ, Biostat & Bioinformat Unit, Cardiff CF14 4XN, S Glam, Wales
[2] Univ Edinburgh, Inst Evolutionary Biol, Edinburgh EH9 3JT, Midlothian, Scotland
关键词
D O I
10.1534/genetics.105.043828
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
There is currently considerable interest in genetic analysis of quantitative traits such as blood pressure and body mass index. Despite the fact that these traits change throughout life they are commonly analyzed only at a single time point. The genetic basis of such traits can be better understood by collecting and effectively analyzing longitudinal data. Analyses of these data are complicated by the need to incorporate information from complex pedigree structures and genetic markers. We propose conducting longitudinal quantitative trait locus (QTL) analyses on such data sets by using a flexible random regression estimation technique. The relationship between genetic effects at different ages is efficiently modeled using covariance functions (CFs). Using simulated data we show that the change in genetic effects over time can be well characterized using CFs and that including parameters to model the change in effect with age can provide substantial increases in power to detect QTL compared with repeated measure or univariate techniques. The asymptotic distributions of the methods used are investigated and methods for overcoming the practical difficulties in fitting CFs are discussed. The CF-based techniques should allow efficient multivariate analyses of many data sets in human and natural population genetics.
引用
收藏
页码:1365 / 1376
页数:12
相关论文
共 47 条
[1]   Multiple phenotype modeling in gene-mapping studies of quantitative traits: Power advantages [J].
Allison, DB ;
Thiel, B ;
St Jean, P ;
Elston, RC ;
Infante, MC ;
Schork, NJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) :1190-1201
[2]   Genetic analysis workshop 13: Introduction to workshop summaries [J].
Almasy, L ;
Cupples, LA ;
Daw, EW ;
Levy, D ;
Thomas, D ;
Rice, JP ;
Santangelo, S ;
MacCluer, JW .
GENETIC EPIDEMIOLOGY, 2003, 25 :S1-S4
[3]   Multipoint quantitative-trait linkage analysis in general pedigrees [J].
Almasy, L ;
Blangero, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (05) :1198-1211
[4]   Comparison of multivariate tests for genetic linkage [J].
Amos, CI ;
de Andrade, M ;
Zhu, DK .
HUMAN HEREDITY, 2001, 51 (03) :133-144
[5]  
AMOS CI, 1990, AM J HUM GENET, V47, P247
[6]  
AMOS CI, 1994, AM J HUM GENET, V54, P535
[7]   MULTIVARIATE SEGREGATION ANALYSIS USING THE MIXED MODEL [J].
BLANGERO, J ;
KONIGSBERG, LW .
GENETIC EPIDEMIOLOGY, 1991, 8 (05) :299-316
[8]   A comparison of power to detect a QTL in sib-pair data using multivariate phenotypes, mean phenotypes, and factor scores [J].
Boomsma, DI ;
Dolan, CV .
BEHAVIOR GENETICS, 1998, 28 (05) :329-340
[9]   Comparison of longitudinal variance components and regression-based approaches for linkage detection on chromosome 17 for systolic blood pressure [J].
de Andrade, M ;
Olswold, C .
BMC GENETICS, 2003, 4 (Suppl 1)
[10]   Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis [J].
de Andrade, M ;
Guéguen, R ;
Visvikis, S ;
Sass, C ;
Siest, G ;
Amos, CI .
GENETIC EPIDEMIOLOGY, 2002, 22 (03) :221-232