Common Variants Show Predicted Polygenic Effects on Height in the Tails of the Distribution, Except in Extremely Short Individuals

被引:38
作者
Chan, Yingleong [1 ,2 ,3 ]
Holmen, Oddgeir L. [4 ,5 ]
Dauber, Andrew [2 ,3 ]
Vatten, Lars [6 ]
Havulinna, Aki S. [7 ]
Skorpen, Frank [8 ]
Kvaloy, Kirsti [4 ]
Silander, Kaisa [7 ,9 ]
Nguyen, Thutrang T. [3 ]
Willer, Cristen [10 ]
Boehnke, Michael [10 ]
Perola, Markus [7 ,9 ,11 ]
Palotie, Aarno [2 ,9 ,12 ,13 ,14 ]
Salomaa, Veikko [7 ]
Hveem, Kristian [4 ]
Frayling, Timothy M. [15 ]
Hirschhorn, Joel N. [1 ,2 ,3 ]
Weedon, Michael N. [15 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02115 USA
[2] Broad Inst, Cambridge, MA USA
[3] Childrens Hosp Boston, Boston, MA USA
[4] Norwegian Univ Sci & Technol, HUNT Res Ctr, Dept Publ Hlth & Gen Practice, Levanger, Norway
[5] Univ Trondheim Hosp, St Olav Hosp, Trondheim, Norway
[6] Norwegian Univ Sci & Technol, Dept Publ Hlth & Gen Practice, N-7034 Trondheim, Norway
[7] Natl Inst Hlth & Welf, Helsinki, Finland
[8] Norwegian Univ Sci & Technol, Dept Lab Med Childrens & Womens Hlth, N-7034 Trondheim, Norway
[9] Univ Helsinki, FIMM, Helsinki, Finland
[10] Univ Michigan, Dept Internal Med, Div Cardiovasc Med, Ann Arbor, MI 48109 USA
[11] Univ Tartu, Estonian Genome Project, EE-50090 Tartu, Estonia
[12] Wellcome Trust Sanger Inst, Hinxton, England
[13] Univ Helsinki, Dept Med Genet, Helsinki, Finland
[14] Univ Cent Hosp, Helsinki, Finland
[15] Univ Exeter, Peninsula Med Sch, Exeter, Devon, England
来源
PLOS GENETICS | 2011年 / 7卷 / 12期
基金
芬兰科学院; 英国惠康基金;
关键词
QUANTITATIVE TRAITS; MISSING HERITABILITY; LINKAGE; ASSOCIATION; POWER; STRATEGIES; TOOL;
D O I
10.1371/journal.pgen.1002439
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Common genetic variants have been shown to explain a fraction of the inherited variation for many common diseases and quantitative traits, including height, a classic polygenic trait. The extent to which common variation determines the phenotype of highly heritable traits such as height is uncertain, as is the extent to which common variation is relevant to individuals with more extreme phenotypes. To address these questions, we studied 1,214 individuals from the top and bottom extremes of the height distribution (tallest and shortest similar to 1.5%), drawn from similar to 78,000 individuals from the HUNT and FINRISK cohorts. We found that common variants still influence height at the extremes of the distribution: common variants (49/141) were nominally associated with height in the expected direction more often than is expected by chance (p<5 x 10(-28)), and the odds ratios in the extreme samples were consistent with the effects estimated previously in population-based data. To examine more closely whether the common variants have the expected effects, we calculated a weighted allele score (WAS), which is a weighted prediction of height for each individual based on the previously estimated effect sizes of the common variants in the overall population. The average WAS is consistent with expectation in the tall individuals, but was not as extreme as expected in the shortest individuals (p<0.006), indicating that some of the short stature is explained by factors other than common genetic variation. The discrepancy was more pronounced (p < 10(-6)) in the most extreme individuals (height <0.25 percentile). The results at the extreme short tails are consistent with a large number of models incorporating either rare genetic non-additive or rare non-genetic factors that decrease height. We conclude that common genetic variants are associated with height at the extremes as well as across the population, but that additional factors become more prominent at the shorter extreme.
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页数:11
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