Heritability of cardiovascular and personality traits in 6,148 sardinians

被引:400
作者
Pilia, Giuseppe
Chen, Wei-Min
Scuteri, Angelo
Orru, Marco
Albai, Giuseppe
Dei, Mariano
Lai, Sandra
Usala, Gianluca
Lai, Monica
Loi, Paola
Mameli, Cinzia
Vacca, Loredana
Deiana, Manila
Olla, Nazario
Masala, Marco
Cao, Antonio
Najjar, Samer S.
Terracciano, Antonio
Nedorezov, Timur
Sharov, Alexei
Zonderman, Alan B.
Abecasis, Goncalo R.
Costa, Paul
Lakatta, Edward
Schlessinger, David
机构
[1] NIA, Gerontol Res Ctr, Baltimore, MD 21224 USA
[2] Osped Microcitem, Ist Neurogenet & Neurofarmacol, Consiglio Nazl Ric, Cagliari, Italy
[3] Univ Michigan, Dept Biostat, Ctr Stat Genet, Ann Arbor, MI 48109 USA
[4] Ist Nazl Riposa & Cura Anziani, Unita Operat, Rome, Italy
[5] Presidio Osped Santa Barbara, Unit Operat Semplice Cardiol, Div Med, Iglesias, Italy
来源
PLOS GENETICS | 2006年 / 2卷 / 08期
关键词
D O I
10.1371/journal.pgen.0020132
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In family studies, phenotypic similarities between relatives yield information on the overall contribution of genes to trait variation. Large samples are important for these family studies, especially when comparing heritability between subgroups such as young and old, or males and females. We recruited a cohort of 6,148 participants, aged 14-102 y, from four clustered towns in Sardinia. The cohort includes 34,469 relative pairs. To extract genetic information, we implemented software for variance components heritability analysis, designed to handle large pedigrees, analyze multiple traits simultaneously, and model heterogeneity. Here, we report heritability analyses for 98 quantitative traits, focusing on facets of personality and cardiovascular function. We also summarize results of bivariate analyses for all pairs of traits and of heterogeneity analyses for each trait. We found a significant genetic component for every trait. On average, genetic effects explained 40% of the variance for 38 blood tests, 51% for five anthropometric measures, 25% for 20 measures of cardiovascular function, and 19% for 35 personality traits. Four traits showed significant evidence for an X-linked component. Bivariate analyses suggested overlapping genetic determinants for many traits, including multiple personality facets and several traits related to the metabolic syndrome; but we found no evidence for shared genetic determinants that might underlie the reported association of some personality traits and cardiovascular risk factors. Models allowing for heterogeneity suggested that, in this cohort, the genetic variance was typically larger in females and in younger individuals, but interesting exceptions were observed. For example, narrow heritability of blood pressure was approximately 26% in individuals more than 42 y old, but only approximately 8% in younger individuals. Despite the heterogeneity in effect sizes, the same loci appear to contribute to variance in young and old, and in males and females. In summary, we find significant evidence for heritability of many medically important traits, including cardiovascular function and personality. Evidence for heterogeneity by age and sex suggests that models allowing for these differences will be important in mapping quantitative traits.
引用
收藏
页码:1207 / 1223
页数:17
相关论文
共 71 条
[1]   A general test of association for quantitative traits in nuclear families [J].
Abecasis, GR ;
Cardon, LR ;
Cookson, WOC .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :279-292
[2]   Broad and narrow heritabilities of quantitative traits in a founder population [J].
Abney, M ;
McPeek, MS ;
Ober, C .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (05) :1302-1307
[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]  
ANDERSON DE, 2006, IN PRESS AM J HYPERT
[5]   A new essential hypertension susceptibility locus on chromosome 2p24-p25, detected by genomewide search [J].
Angius, A ;
Petretto, E ;
Maestrale, GB ;
Forabosco, P ;
Casu, G ;
Piras, D ;
Fanciulli, M ;
Falchi, M ;
Melis, PM ;
Palermo, M ;
Pirastu, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) :893-905
[6]  
Bathum L, 2001, CLIN CHEM, V47, P81
[7]   CONTROLLING THE FALSE DISCOVERY RATE - A PRACTICAL AND POWERFUL APPROACH TO MULTIPLE TESTING [J].
BENJAMINI, Y ;
HOCHBERG, Y .
JOURNAL OF THE ROYAL STATISTICAL SOCIETY SERIES B-STATISTICAL METHODOLOGY, 1995, 57 (01) :289-300
[8]   Carotid intima-media thickness, arterial stiffness and risk of cardiovascular disease: current evidence [J].
Bots, ML ;
Dijk, JM ;
Oren, A ;
Grobbee, DE .
JOURNAL OF HYPERTENSION, 2002, 20 (12) :2317-2325
[9]  
Bouchard Thomas J., 1997, HDB PSYCHIAT GENETIC, P273
[10]  
Bouchard TJ, 2001, BEHAV GENET, V31, P243