Suppr超能文献

遗传变异影响注意缺陷多动障碍患者的大脑变化。

Genetic variations influence brain changes in patients with attention-deficit hyperactivity disorder.

机构信息

Laboratory of Molecular and Metabolic Imaging, Sidra Medicine, Doha, Qatar.

Department of Pediatrics, Sidra Medicine, Doha, Qatar.

出版信息

Transl Psychiatry. 2021 Jun 5;11(1):349. doi: 10.1038/s41398-021-01473-w.

Abstract

Attention-deficit hyperactivity disorder (ADHD) is a neurological and neurodevelopmental childhood-onset disorder characterized by a persistent pattern of inattentiveness, impulsiveness, restlessness, and hyperactivity. These symptoms may continue in 55-66% of cases from childhood into adulthood. Even though the precise etiology of ADHD is not fully understood, it is considered as a multifactorial and heterogeneous disorder with several contributing factors such as heritability, auxiliary to neurodevelopmental issues, severe brain injuries, neuroinflammation, consanguineous marriages, premature birth, and exposure to environmental toxins. Neuroimaging and neurodevelopmental assessments may help to explore the possible role of genetic variations on ADHD neuropsychobiology. Multiple genetic studies have observed a strong genetic association with various aspects of neuropsychobiological functions, including neural abnormalities and delayed neurodevelopment in ADHD. The advancement in neuroimaging and molecular genomics offers the opportunity to analyze the impact of genetic variations alongside its dysregulated pathways on structural and functional derived brain imaging phenotypes in various neurological and psychiatric disorders, including ADHD. Recently, neuroimaging genomic studies observed a significant association of brain imaging phenotypes with genetic susceptibility in ADHD. Integrating the neuroimaging-derived phenotypes with genomics deciphers various neurobiological pathways that can be leveraged for the development of novel clinical biomarkers, new treatment modalities as well as therapeutic interventions for ADHD patients. In this review, we discuss the neurobiology of ADHD with particular emphasis on structural and functional changes in the ADHD brain and their interactions with complex genomic variations utilizing imaging genetics methodologies. We also highlight the genetic variants supposedly allied with the development of ADHD and how these, in turn, may affect the brain circuit function and related behaviors. In addition to reviewing imaging genetic studies, we also examine the need for complementary approaches at various levels of biological complexity and emphasize the importance of combining and integrating results to explore biological pathways involved in ADHD disorder. These approaches include animal models, computational biology, bioinformatics analyses, and multimodal imaging genetics studies.

摘要

注意缺陷多动障碍(ADHD)是一种神经发育障碍,以持续存在的注意力不集中、冲动、不安和多动为特征。这些症状在 55-66%的病例中可能会从儿童期持续到成年期。尽管 ADHD 的确切病因尚未完全了解,但它被认为是一种多因素和异质性疾病,有几个促成因素,如遗传性、神经发育问题、严重脑损伤、神经炎症、近亲结婚、早产和暴露于环境毒素。神经影像学和神经发育评估可以帮助探索遗传变异对 ADHD 神经生物学的可能作用。多项遗传研究观察到遗传变异与神经心理生物学的各个方面有很强的关联性,包括 ADHD 中的神经异常和神经发育延迟。神经影像学和分子基因组学的进步提供了机会,可以分析遗传变异及其失调途径对各种神经和精神疾病(包括 ADHD)的结构和功能衍生脑成像表型的影响。最近,神经影像学基因组研究观察到 ADHD 中脑成像表型与遗传易感性的显著关联。将神经影像学衍生的表型与基因组学相结合,可以解析出各种神经生物学途径,这些途径可以为 ADHD 患者开发新的临床生物标志物、新的治疗方法和治疗干预措施提供依据。在这篇综述中,我们讨论了 ADHD 的神经生物学,特别强调了 ADHD 大脑的结构和功能变化及其与复杂基因组变异的相互作用,利用了影像遗传学方法。我们还强调了与 ADHD 发展相关的遗传变异,以及这些遗传变异如何反过来影响大脑回路功能和相关行为。除了综述影像遗传学研究外,我们还探讨了在各个层次的生物学复杂性上需要互补方法,并强调了结合和整合结果以探索 ADHD 障碍中涉及的生物学途径的重要性。这些方法包括动物模型、计算生物学、生物信息学分析和多模态影像遗传学研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f430/8179928/ca44fc50cdbf/41398_2021_1473_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验