失読症とADHDには遺伝的なつながりがあることが研究で明らかに(Dyslexia and ADHD share genetic links, study shows)

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2024-09-10 エディンバラ大学

エディンバラ大学の研究により、ディスレクシア(読字障害)と注意欠陥多動性障害(ADHD)の遺伝的関連性が明らかになりました。これら2つの障害は多くの共通する遺伝子を持ち、発達障害や精神的疾患(自閉症、双極性障害、統合失調症など)とは異なる特徴を持つことが示されています。約100万人の遺伝データを用いた解析で、ディスレクシアとADHDに共通する49の遺伝領域と174の遺伝子が特定されました。この研究は、将来的に教育や福祉支援に役立つ可能性があり、遺伝的要因の理解が進むことで新しいサポート方法が期待されます。

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G遺伝的神経発達クラスターと失読症 enetic neurodevelopmental clustering and dyslexia

Austeja Ciulkinyte,Hayley S. Mountford,Pierre Fontanillas,23andMe Research Team,Timothy C. Bates,Nicholas G. Martin,Simon E. Fisher & Michelle Luciano
Molecular Psychiatry  Published:15 July 2024
DOI:https://doi.org/10.1038/s41380-024-02649-8

失読症とADHDには遺伝的なつながりがあることが研究で明らかに(Dyslexia and ADHD share genetic links, study shows)

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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