Weinberg C R
Biostatistics Branch, National Institute of Environmental Health Sciences, Research Triangle Park, NC, USA
Am J Hum Genet. 1999 Jul;65(1):229-35. doi: 10.1086/302466.
When affected probands and their biological parents are genotyped at a candidate gene or a marker, the resulting case-parents-triad data enable powerful tests for linkage in the presence of association. When linkage disequilibrium has been detected in such a study, the investigator may wish to look further for possible parent-of-origin effects. If, for example, the transmission/disequilibrium test restricted to fathers is statistically significant, whereas that restricted to mothers is not, the investigator might interpret this as evidence for nonexpression of the maternally derived disease gene-that is, imprinting. This report reviews existing methods for detection of parent-of-origin effects, showing that each can be invalid under certain scenarios. Two new methods are proposed, based on application of likelihood-based inference after stratification on both the parental mating type and the inherited number of copies of the allele under study. If there are no maternal genetic effects expressed prenatally during gestation, the parental-asymmetry test is powerful and provides valid estimation of a parent-of-origin parameter. For diseases for which there could be maternal effects on risk, the parent-of-origin likelihood-ratio test provides a robust alternative. Simulations based on an admixed population demonstrate good operating characteristics for these procedures, under diverse scenarios.
当对受影响的先证者及其生物学父母进行候选基因或标记的基因分型时,由此产生的病例 - 父母三联体数据能够在存在关联的情况下进行强大的连锁检验。当在此类研究中检测到连锁不平衡时,研究者可能希望进一步寻找可能的亲本来源效应。例如,如果仅针对父亲的传递/不平衡检验具有统计学意义,而仅针对母亲的检验无统计学意义,研究者可能将此解释为母源疾病基因不表达的证据,即印记。本报告回顾了现有的检测亲本来源效应的方法,表明每种方法在某些情况下都可能无效。基于对亲本交配类型和所研究等位基因的遗传拷贝数进行分层后应用似然推断,提出了两种新方法。如果在妊娠期间产前没有母源遗传效应表达,亲本不对称检验效力强大,并能有效估计亲本来源参数。对于可能存在母源风险效应的疾病,亲本来源似然比检验提供了一种可靠的替代方法。基于混合人群的模拟显示,在不同情况下这些方法具有良好的操作特性。