Lemire Mathieu, Roslin Nicole M, Laprise Catherine, Hudson Thomas J, Morgan Kenneth
McGill University and Genome Quebec Innovation Centre, and Departments of Human Genetics and Medicine, McGill University, Montreal, Quebec, Canada.
Am J Hum Genet. 2004 Oct;75(4):571-86. doi: 10.1086/424528. Epub 2004 Aug 20.
We studied the effect of transmission-ratio distortion (TRD) on tests of linkage based on allele sharing in affected sib pairs. We developed and implemented a discrete-trait allele-sharing test statistic, Sad, analogous to the Spairs test statistic of Whittemore and Halpern, that evaluates an excess sharing of alleles at autosomal loci in pairs of affected siblings, as well as a lack of sharing in phenotypically discordant relative pairs, where available. Under the null hypothesis of no linkage, nuclear families with at least two affected siblings and one unaffected sibling have a contribution to Sad that is unbiased, with respect to the effects of TRD independent of the disease under study. If more distantly related unaffected individuals are studied, the bias of Sad is generally reduced compared with that of Spairs, but not completely. Moreover, Sad has higher power, in some circumstances, because of the availability of unaffected relatives, who are ignored in affected-only analyses. We discuss situations in which it may be an efficient use of resources to genotype unaffected relatives, which would give insights for promising study designs. The method is applied to a sample of pedigrees ascertained for asthma in a chromosomal region in which TRD has been reported. Results are consistent with the presence of transmission distortion in that region.
我们研究了传递不平衡(TRD)对基于患病同胞对中基因共享的连锁分析检验的影响。我们开发并实施了一种离散性状基因共享检验统计量Sad,它类似于Whittemore和Halpern的Spairs检验统计量,用于评估患病同胞对中常染色体位点上等位基因的过度共享,以及在可获得的表型不一致的亲属对中基因共享的缺乏情况。在无连锁的零假设下,至少有两个患病同胞和一个未患病同胞的核心家庭对Sad的贡献是无偏的,这与所研究疾病无关的TRD效应无关。如果研究更远亲的未患病个体,与Spairs相比,Sad的偏差通常会减小,但不会完全消除。此外,在某些情况下,Sad具有更高的检验效能,因为未患病亲属的存在在仅针对患病个体的分析中被忽略了。我们讨论了对未患病亲属进行基因分型可能是有效利用资源的情况,这将为有前景的研究设计提供思路。该方法应用于一个在已报道存在TRD的染色体区域中因哮喘而确定的家系样本。结果与该区域存在传递畸变一致。