Genetic neurodevelopmental clustering and dyslexia.

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Psychiatry Pub Date : 2024-07-15 DOI:10.1038/s41380-024-02649-8
Austeja Ciulkinyte, Hayley S Mountford, Pierre Fontanillas, Timothy C Bates, Nicholas G Martin, Simon E Fisher, Michelle Luciano
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Abstract

Dyslexia is a learning difficulty with neurodevelopmental origins, manifesting as reduced accuracy and speed in reading and spelling. It is substantially heritable and frequently co-occurs with other neurodevelopmental conditions, particularly attention deficit-hyperactivity disorder (ADHD). Here, we investigate the genetic structure underlying dyslexia and a range of psychiatric traits using results from genome-wide association studies of dyslexia, ADHD, autism, anorexia nervosa, anxiety, bipolar disorder, major depressive disorder, obsessive compulsive disorder, schizophrenia, and Tourette syndrome. Genomic Structural Equation Modelling (GenomicSEM) showed heightened support for a model consisting of five correlated latent genomic factors described as: F1) compulsive disorders (including obsessive-compulsive disorder, anorexia nervosa, Tourette syndrome), F2) psychotic disorders (including bipolar disorder, schizophrenia), F3) internalising disorders (including anxiety disorder, major depressive disorder), F4) neurodevelopmental traits (including autism, ADHD), and F5) attention and learning difficulties (including ADHD, dyslexia). ADHD loaded more strongly on the attention and learning difficulties latent factor (F5) than on the neurodevelopmental traits latent factor (F4). The attention and learning difficulties latent factor (F5) was positively correlated with internalising disorders (.40), neurodevelopmental traits (.25) and psychotic disorders (.17) latent factors, and negatively correlated with the compulsive disorders (-.16) latent factor. These factor correlations are mirrored in genetic correlations observed between the attention and learning difficulties latent factor and other cognitive, psychological and wellbeing traits. We further investigated genetic variants underlying both dyslexia and ADHD, which implicated 49 loci (40 not previously found in GWAS of the individual traits) mapping to 174 genes (121 not found in GWAS of individual traits) as potential pleiotropic variants. Our study confirms the increased genetic relation between dyslexia and ADHD versus other psychiatric traits and uncovers novel pleiotropic variants affecting both traits. In future, analyses including additional co-occurring traits such as dyscalculia and dyspraxia will allow a clearer definition of the attention and learning difficulties latent factor, yielding further insights into factor structure and pleiotropic effects.

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遗传性神经发育集群和阅读障碍。
阅读障碍是一种源于神经发育的学习困难,表现为阅读和拼写的准确性和速度降低。阅读障碍具有很强的遗传性,并且经常与其他神经发育疾病并发,尤其是注意力缺陷多动障碍(ADHD)。在此,我们利用对阅读障碍、多动症、自闭症、神经性厌食症、焦虑症、双相情感障碍、重度抑郁症、强迫症、精神分裂症和抽动秽语综合征进行的全基因组关联研究的结果,研究阅读障碍和一系列精神疾病特征的遗传结构。基因组结构方程模型(GenomicSEM)显示,由五个相关的潜在基因组因素组成的模型得到了更多的支持,这五个潜在基因组因素分别是F1)强迫症(包括强迫症、神经性厌食症、抽动秽语综合征);F2)精神病(包括躁郁症、精神分裂症);F3)内化性障碍(包括焦虑症、重度抑郁症);F4)神经发育特征(包括自闭症、多动症);F5)注意力和学习困难(包括多动症、阅读障碍)。多动症在注意力和学习困难潜因子(F5)上的负荷比在神经发育特征潜因子(F4)上的负荷更强。注意力和学习困难潜因子(F5)与内化障碍(0.40)、神经发育特征(0.25)和精神障碍(0.17)潜因子呈正相关,与强迫症(-0.16)潜因子呈负相关。注意力和学习困难潜因子与其他认知、心理和福利特征之间的遗传相关性也反映了这些因子的相关性。我们进一步研究了阅读障碍和多动症的遗传变异,结果发现有 49 个基因位点(其中 40 个位点以前在单个性状的全球基因组研究中未发现)与 174 个基因(其中 121 个基因在单个性状的全球基因组研究中未发现)的映射关系可能是多向变异。我们的研究证实,相对于其他精神特质,阅读障碍和多动症之间的遗传关系更为密切,并发现了影响这两种特质的新型多向变异。今后,在分析中纳入更多的共存性状,如计算障碍和障碍,将能更清晰地定义注意力和学习困难的潜在因子,从而进一步了解因子结构和多向效应。
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来源期刊
Molecular Psychiatry
Molecular Psychiatry 医学-精神病学
CiteScore
20.50
自引率
4.50%
发文量
459
审稿时长
4-8 weeks
期刊介绍: Molecular Psychiatry focuses on publishing research that aims to uncover the biological mechanisms behind psychiatric disorders and their treatment. The journal emphasizes studies that bridge pre-clinical and clinical research, covering cellular, molecular, integrative, clinical, imaging, and psychopharmacology levels.
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