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[与发育性阅读障碍相关的心理认知和精神障碍:一个临床与科学问题]

[Psychocognitive and psychiatric disorders associated with developmental dyslexia: A clinical and scientific issue].

作者信息

Huc-Chabrolle M, Barthez M-A, Tripi G, Barthélémy C, Bonnet-Brilhault F

机构信息

UMR Inserm U, CNRS FRE, université François-Rabelais de Tours, France.

出版信息

Encephale. 2010 Apr;36(2):172-9. doi: 10.1016/j.encep.2009.02.005. Epub 2009 Jun 10.

Abstract

INTRODUCTION

Dyslexia is a complex neurodevelopemental disorder that affects 5 to 10% of school-age children. This condition consists in a specific learning disability with a neurological origin. These learning difficulties are unexpected in relation to other cognitive abilities and the provision of efficient classroom instruction. A range of neurobiological investigations suggests that disruption of the parieto-temporo-occipital systems underlies a failure of skilled reading to develop. The observation that dyslexia is both a familial and heritable problem was made early on and was confirmed by twin studies. They also suggested that both genetic and environmental factors are involved. Several loci have been implicated in dyslexia, notably on chromosomes 2, 3, 6, 15 and 18 and some candidate genes have been proposed, but no functional mutation has yet been identified.

LITERATURE REVIEW

Dyslexia seldom appears isolated and dyslexic people are very likely to present other kinds of learning disabilities or psychiatric disorders. Specific language impairment, often with a mild outcome, is the most frequently associated with dyslexia. Indeed, late language development is often reported by dyslexic patients and also occurs more frequently among their siblings. Genetic linkage studies suggest some common genetic factor underlying this comorbidity. Dyscalculia is associated with dyslexia in 25% of cases, but most people with dyscalculia do not have any sign of dyslexia. The question of whether dyscalculia associated with dyslexia and dyscalculia itself rely on the same cognitive impairment is still controversial. Impaired motor development is also a common feature that affects nearly 50% of dyslexics and dyslexia is frequent among dyspraxic patients. This association raises the discussion on the role of motor impairment in dyslexia's physiopathology and the cerebellar theory of dyslexia. Beyond its link with other learning disorders, the study of dyslexia's comorbidity highlights psychopathological issues. ADHD is the most frequent psychiatric disorder associated with dyslexia. Underpinnings of this link between the two disorders seem to rely on common cognitive and genetic factors. Some authors have proposed a candidate gene ADRA2A to determine the condition including ADHD and dyslexia. In addition, dyslexics are exposed to a higher risk of anxiodepressive and behavioural disorders. Dyslexic children experience three times more behavioural disorders and one third of children with behavioural problems turn out to be affected by dyslexia. The literature study reveals inconsistent findings about depressed mood among dyslexics, but evidence of a persistent increase in the rate of anxiety disorders. The authors put forward the impact of environmental factors to explain these psychiatric comorbidities.

CONCLUSION

This review emphasizes dyslexia's comorbidities because they represent an important issue, both from a scientific and clinical point of view. Indeed, for clinicians, children showing multiple learning disabilities have specific reeducation and educational needs and dyslexics have a higher risk of emotional and behavioural disorders. On the other hand, dyslexia's comorbidity study provides a powerful method for researchers to investigate the still unknown physiopathology of dyslexia.

摘要

引言

诵读困难是一种复杂的神经发育障碍,影响5%至10%的学龄儿童。这种病症表现为具有神经学根源的特定学习障碍。相对于其他认知能力以及高效课堂教学的提供而言,这些学习困难是出人意料的。一系列神经生物学研究表明,顶颞枕系统的紊乱是导致熟练阅读能力无法发展的根本原因。诵读困难是一种家族性和遗传性问题这一观察结果很早就已得出,并得到了双胞胎研究的证实。这些研究还表明,遗传因素和环境因素都有涉及。有几个基因座与诵读困难有关,特别是在2号、3号、6号、15号和18号染色体上,并且已经提出了一些候选基因,但尚未鉴定出功能性突变。

文献综述

诵读困难很少单独出现,诵读困难者很可能还存在其他类型的学习障碍或精神疾病。特定语言障碍,通常预后较轻,是与诵读困难最常相关的疾病。事实上,诵读困难患者经常报告语言发育迟缓,并且在他们的兄弟姐妹中也更频繁地出现。遗传连锁研究表明,这种共病存在一些共同的遗传因素。25%的病例中,计算障碍与诵读困难相关,但大多数计算障碍患者没有任何诵读困难的迹象。与诵读困难相关的计算障碍和计算障碍本身是否依赖于相同的认知损伤这一问题仍存在争议。运动发育受损也是一个常见特征,影响近50%的诵读困难者,并且在运动障碍患者中诵读困难也很常见。这种关联引发了关于运动障碍在诵读困难病理生理学中的作用以及诵读困难的小脑理论的讨论。除了与其他学习障碍的联系之外,对诵读困难共病的研究还突出了精神病理学问题。注意力缺陷多动障碍(ADHD)是与诵读困难最常相关的精神疾病。这两种疾病之间联系的基础似乎依赖于共同的认知和遗传因素。一些作者提出候选基因ADRA2A来确定包括ADHD和诵读困难在内的病症。此外,诵读困难者患焦虑抑郁和行为障碍的风险更高。诵读困难儿童出现行为障碍的几率是其他儿童的三倍,并且三分之一有行为问题的儿童被证明患有诵读困难。文献研究揭示了关于诵读困难者抑郁情绪的不一致结果,但有证据表明焦虑症的发病率持续上升。作者提出环境因素的影响来解释这些精神共病。

结论

本综述强调诵读困难的共病情况,因为从科学和临床角度来看,它们都是一个重要问题。事实上,对于临床医生来说,表现出多种学习障碍的儿童有特定的再教育和教育需求,而诵读困难者有更高的情绪和行为障碍风险。另一方面,诵读困难的共病研究为研究人员调查诵读困难仍未知的病理生理学提供了一种有力方法。

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