Multivariate variance-components analysis of longitudinal blood pressure measurements from the Framingham Heart Study

被引:17
作者
Kraft, P [1 ]
Bauman, L
Yuan, JY
Horvath, S
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[2] Univ Calif Los Angeles, Dept Biomath, Los Angeles, CA USA
[3] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA USA
[4] Univ Calif Los Angeles, Dept Biostat, Los Angeles, CA USA
关键词
D O I
10.1186/1471-2156-4-S1-S55
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Multivariate variance-components analysis provides several advantages over univariate analysis when studying correlated traits. It can test for pleiotropy or ( in the longitudinal context) gene x age interaction. It can also have more power than univariate analyses to detect a quantitative trait locus influencing several traits. We apply multivariate variance components to longitudinal systolic blood pressure data from the Framingham Heart Study. We find evidence for a polygenic influence on blood pressure ( heritabilities at different ages range from 27% to 38%). Tests based on a factor-analytic parameterization of the polygenic variance find significant ( p < 2 x 10(-3)) evidence that different genes affect blood pressure at different ages. Still, estimates for the proportion of polygenic variance due to shared genes ran as high as 85% for some trait pairs. Univariate and multivariate linkage analyses replicate previous linkage results on chromosome 17 ( maximum LOD scores of 2.2 and 2.4, respectively). In this study, multivariate analysis provides no increase in power; this is likely due to the strong positive correlation in systolic blood pressure measured at different ages.
引用
收藏
页数:6
相关论文
共 21 条
[1]  
Almasy L, 1997, GENET EPIDEMIOL, V14, P953, DOI 10.1002/(SICI)1098-2272(1997)14:6<953::AID-GEPI65>3.0.CO
[2]  
2-K
[3]   Detecting genotype x age interaction [J].
Almasy, L ;
Towne, B ;
Peterson, C ;
Blangero, J .
GENETIC EPIDEMIOLOGY, 2001, 21 :S819-S824
[4]   Comparison of multivariate tests for genetic linkage [J].
Amos, CI ;
de Andrade, M ;
Zhu, DK .
HUMAN HEREDITY, 2001, 51 (03) :133-144
[5]  
[Anonymous], 2001, MISSING DATA
[6]  
BLANGERO J, 1993, HUM BIOL, V65, P941
[7]   UNIVARIATE AND BIVARIATE ANALYSES OF CHOLESTEROL AND TRIGLYCERIDE LEVELS IN PEDIGREES [J].
BOEHNKE, M ;
MOLL, PP ;
LANGE, K ;
WEIDMAN, WH ;
KOTTKE, BA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (03) :775-792
[8]  
Cheverud JM, 1996, GENETICS, V142, P1305
[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