Department of Genetics, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS Genet. 2011 Dec;7(12):e1002439. doi: 10.1371/journal.pgen.1002439. Epub 2011 Dec 29.
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 ∼1.5%), drawn from ∼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<5×10⁻²⁸), 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.
常见的遗传变异已经被证明可以解释许多常见疾病和数量性状(包括身高)的遗传变异的一部分,身高是一个经典的多基因性状。常见变异在多大程度上决定了高度遗传的性状(如身高)的表型尚不确定,常见变异与表型更为极端的个体有多相关也不确定。为了解决这些问题,我们研究了来自 HUNT 和 FINRISK 队列的约 78000 个人中身高分布最高和最低极端(最高和最矮约 1.5%)的 1214 个人。我们发现常见变异仍然会影响分布极端的身高:常见变异(49/141)在预期方向上与身高的关联比随机预期更频繁(p<5×10⁻²⁸),极端样本中的优势比与之前在基于人群的数据中估计的效果一致。为了更仔细地检查常见变异是否具有预期的效果,我们计算了加权等位基因评分(WAS),这是根据常见变异在整个人群中的先前估计效应大小对每个个体的身高进行加权预测。在高个子个体中,平均 WAS 与预期一致,但在最矮的个体中并不像预期的那样极端(p<0.006),表明一些矮小身材是由除常见遗传变异以外的因素造成的。在最极端的个体(身高<0.25 百分位)中,差异更为明显(p<10⁻⁶)。极端短尾的结果与许多模型一致,这些模型都纳入了罕见的遗传非加性或降低身高的罕见非遗传因素。我们得出的结论是,常见遗传变异与人群中的身高以及身高极端情况都有关联,但在更短的极端情况下,其他因素变得更为突出。