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语音短期记忆和语法形态在特定语言障碍中的遗传及表型效应。

Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.

作者信息

Falcaro M, Pickles A, Newbury D F, Addis L, Banfield E, Fisher S E, Monaco A P, Simkin Z, Conti-Ramsden G

机构信息

Faculty of Medical and Human Sciences, The University of Manchester, Manchester, United Kingdom.

出版信息

Genes Brain Behav. 2008 Jun;7(4):393-402. doi: 10.1111/j.1601-183X.2007.00364.x. Epub 2007 Nov 12.

Abstract

Deficits in phonological short-term memory and aspects of verb grammar morphology have been proposed as phenotypic markers of specific language impairment (SLI) with the suggestion that these traits are likely to be under different genetic influences. This investigation in 300 first-degree relatives of 93 probands with SLI examined familial aggregation and genetic linkage of two measures thought to index these two traits, non-word repetition and tense marking. In particular, the involvement of chromosomes 16q and 19q was examined as previous studies found these two regions to be related to SLI. Results showed a strong association between relatives' and probands' scores on non-word repetition. In contrast, no association was found for tense marking when examined as a continuous measure. However, significant familial aggregation was found when tense marking was treated as a binary measure with a cut-off point of -1.5 SD, suggestive of the possibility that qualitative distinctions in the trait may be familial while quantitative variability may be more a consequence of non-familial factors. Linkage analyses supported previous findings of the SLI Consortium of linkage to chromosome 16q for phonological short-term memory and to chromosome 19q for expressive language. In addition, we report new findings that relate to the past tense phenotype. For the continuous measure, linkage was found on both chromosomes, but evidence was stronger on chromosome 19. For the binary measure, linkage was observed on chromosome 19 but not on chromosome 16.

摘要

语音短期记忆缺陷和动词语法形态学方面的缺陷已被提出作为特定语言障碍(SLI)的表型标志物,这表明这些特征可能受到不同的基因影响。这项对93名SLI先证者的300名一级亲属进行的调查,研究了被认为可指示这两种特征的两项指标——非词重复和时态标记——的家族聚集性和基因连锁情况。特别是,由于先前的研究发现16号染色体和19号染色体这两个区域与SLI有关,因此对这两个染色体区域的参与情况进行了研究。结果显示,亲属和先证者在非词重复测试中的得分之间存在很强的相关性。相比之下,将时态标记作为连续变量进行检测时,未发现相关性。然而,当时态标记被视为一个以-1.5标准差为分界点的二元变量时,发现了显著的家族聚集性,这表明该特征的质性差异可能具有家族性,而量性变异可能更多是由非家族因素导致的。连锁分析支持了SLI联盟先前的研究结果,即语音短期记忆与16号染色体连锁,表达性语言与19号染色体连锁。此外,我们报告了与过去时表型相关的新发现。对于连续变量,在两条染色体上均发现了连锁,但在19号染色体上的证据更强。对于二元变量,在19号染色体上观察到了连锁,但在16号染色体上未观察到。

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