Evans David M, Duffy David L
Queensland Institute of Medical Research and Joint Genetics Program, University of Queensland, PO Royal Brisbane Hospital, Brisbane 4029, Australia.
Behav Genet. 2004 Mar;34(2):135-41. doi: 10.1023/B:BEGE.0000013727.15845.f8.
The power of bivariate variance components (VC) linkage analysis is affected by the size and source of the phenotypic correlation between variables. In particular, several authors have suggested that the power to detect linkage is greatest when the quantitative trait locus (QTL) and residual sources of variation induce phenotypic covariation in opposite directions, and that this increase in power is greatest when unique environmental sources of variation induce covariation in the direction opposite to the QTL. The purpose of the present study was to investigate further the effect of varying the residual correlation between variables on the power to detect linkage in a bivariate variance components linkage analysis. Data were simulated for a biallelic QTL that pleiotropically influenced two variables. The power to detect linkage was calculated under a variety of situations in which the proportion of phenotypic covariance resulting from shared sources of variation and from unique sources of variation was varied. These simulations were performed for the case in which the QTL affected the two variables equally and also for the case in which the QTL made unequal contributions to each variable. Our results confirm that the power to detect QTLs in a bivariate test for linkage depends upon the size and source of the residual correlation between variables, being greatest when the QTL and unique environmental sources of variation induce phenotypic covariation in opposite directions. We also found that when the QTL affected the two variables unequally, the power to detect linkage increased markedly as the correlation between unique environmental sources of variation increased from 0.6 to 0.9. Similar results were obtained under a variety of genetic models, including when there were unequal allele frequencies and dominance at the QTL. We suggest that a promising strategy to increase the power to detect QTLs might be to collect data from variables where there is either good observational evidence (e.g., from multivariate structural equation modeling of twin data) or a sound theoretical argument that the QTL and environmental factors induce covariation in opposite directions.
双变量方差成分(VC)连锁分析的效能受变量间表型相关性的大小和来源影响。特别是,几位作者指出,当数量性状基因座(QTL)和残余变异来源在相反方向上诱导表型协变时,检测连锁的效能最大,并且当独特环境变异来源在与QTL相反的方向上诱导协变时,这种效能增加最大。本研究的目的是进一步探讨在双变量方差成分连锁分析中改变变量间残余相关性对检测连锁效能的影响。针对一个对两个变量产生多效性影响的双等位基因QTL进行了数据模拟。在各种情况下计算检测连锁的效能,其中共享变异来源和独特变异来源所导致的表型协方差比例有所不同。这些模拟针对QTL对两个变量产生同等影响的情况以及QTL对每个变量贡献不等的情况进行。我们的结果证实,在双变量连锁检验中检测QTL的效能取决于变量间残余相关性的大小和来源,当QTL和独特环境变异来源在相反方向上诱导表型协变时效能最大。我们还发现,当QTL对两个变量的影响不等时,随着独特环境变异来源之间的相关性从0.6增加到0.9,检测连锁的效能显著增加。在各种遗传模型下都获得了类似结果,包括QTL处等位基因频率不等和存在显性的情况。我们建议,一种提高检测QTL效能的有前景策略可能是从具有良好观察证据(例如,来自双胞胎数据的多变量结构方程建模)或有合理理论依据表明QTL和环境因素在相反方向上诱导协变的变量中收集数据。