Mascheretti Sara, Riva Valentina, Giorda Roberto, Beri Silvana, Lanzoni Lara Francesca Emilia, Cellino Maria Rosaria, Marino Cecilia
Child Psychopathology Unit, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, Lecco, Italy.
Molecular Biology Lab, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, Lecco, Italy.
J Hum Genet. 2014 Apr;59(4):189-97. doi: 10.1038/jhg.2013.141. Epub 2014 Jan 16.
Substantial heritability has been reported for developmental dyslexia (DD), and KIAA0319 and ROBO1 appear as more than plausible candidate susceptibility genes for this developmental disorder. Converging evidence indicates that developmental difficulties in oral language and mathematics can predate or co-occur with DD, and substantial genetic correlations have been found between these abilities and reading traits. In this study, we explored the role of eight single-nucleotide polymorphisms spanning within KIAA0319 and ROBO1 genes, and DD as a dichotomic trait, related neuropsychological phenotypes and comorbid language and mathematical (dis)abilities in a large cohort of 493 Italian nuclear families ascertained through a proband with a diagnosis of DD. Marker-trait association was analyzed by implementing a general test of family-based association for quantitative traits (that is, the Quantitative Transmission Disequilibrium Test, version 2.5.1). By providing evidence for significant association with mathematics skills, our data add further result in support of ROBO1 contributing to the deficits in DD and its correlated phenotypes. Taken together, our findings shed further light into the etiologic basis and the phenotypic complexity of this developmental disorder.
发育性阅读障碍(DD)已被报道具有显著的遗传力,而KIAA0319和ROBO1似乎是这种发育障碍非常有可能的候选易感基因。越来越多的证据表明,口语和数学方面的发育困难可能先于DD出现或与DD同时出现,并且在这些能力与阅读特征之间发现了显著的遗传相关性。在本研究中,我们在一个由493个意大利核心家庭组成的大型队列中,探索了KIAA0319和ROBO1基因内的8个单核苷酸多态性的作用,以及作为二分性状的DD、相关的神经心理学表型以及共病的语言和数学(障碍)能力。通过一名被诊断为DD的先证者确定了这些家庭。通过实施针对数量性状的基于家庭关联的通用检验(即数量传递不平衡检验,版本2.5.1)来分析标记-性状关联。通过提供与数学技能显著关联的证据,我们的数据进一步支持了ROBO1导致DD及其相关表型缺陷的观点。综上所述,我们的研究结果进一步揭示了这种发育障碍的病因基础和表型复杂性。