深度学习算法揭示了一大群唐氏综合症儿童焦虑障碍的基因组标记

IF 9.6 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yichuan Liu, Hui-Qi Qu, Xiao Chang, Frank D. Mentch, Haijun Qiu, Shahram Torkamandi, Kenny Nguyen, Kayleigh Ostberg, Tiancheng Wang, Joseph Glessner, Hakon Hakonarson
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引用次数: 0

摘要

尽管唐氏综合症(DS)儿童有严重的神经行为和精神合并症负担,并且智力残疾(ID)个体的焦虑风险普遍增加,但唐氏综合症儿童的焦虑发生率明显较低。了解退行性椎体滑移中焦虑的具体机制可以为开发新的治疗方法提供信息。这项研究对导致退行性痴呆患者焦虑障碍的基因组变异以及其他精神障碍患者共有的基因组变异进行了全面调查。我们采用深度学习算法,结合神经网络模型和最大的全基因组测序(WGS)队列之一,对1479名DS个体和家庭成员进行了研究,其中包括255名诊断为至少一种精神障碍的DS先证,其中74名确诊为焦虑症。我们发现,只有一小部分(19%)的焦虑特异性相应基因变异与退行性痴呆患者焦虑共有的基因变异重叠,这表明退行性痴呆个体焦虑的不同分子机制。功能过度代表分析表明,焦虑是遗传和环境因素复杂相互作用的结果。此外,非编码变异体,特别是靠近剪接位点的变异体,也起着重要的作用。此外,与焦虑和其他精神障碍相关的变异并不是唯一分布在整个基因组中的。包括17q25、16q23、21q22和22q13在内的几个位点在DS患者中显示出更大的重量。此外,29个包含复发性焦虑特异性变异的生物标志物被确定,以帮助诊断退行性痴呆人群的焦虑。这项开创性的研究首次利用WGS队列和先进的深度学习人工智能模型对DS中的焦虑症进行了全面探索。结果表明,退行性椎体滑移患者的焦虑障碍具有不同于其他精神障碍的分子模式。从我们的研究中获得的见解提供了对潜在机制的有价值的理解,并有望加强临床诊断,并可能指导对这一弱势群体更有效的干预策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deep learning algorithms reveal genomic markers for anxiety disorder in a large cohort of children with down syndrome

Deep learning algorithms reveal genomic markers for anxiety disorder in a large cohort of children with down syndrome

Despite a significant burden of neurobehavioral and psychiatric comorbidities in children with Down syndrome (DS), and the general increased risk for anxiety in individuals with intellectual disabilities (ID), children with DS have significantly lower odds of anxiety. Understanding the specific mechanisms of anxiety in DS could inform the development of new treatments. This study performed a comprehensive investigation of genomic variants that contribute to anxiety disorders in DS, as well as variants shared in other mental disorders. We employed deep learning algorithms using neural network models in combination with one of the largest whole-genome sequencing (WGS) cohorts of 1479 DS individuals and family members, including 255 DS probands diagnosed with at least one type of mental disorder, of whom 74 had confirmed anxiety disorders. We found that only a fraction (19%) of anxiety-specific corresponding gene variants previously reported overlap with those shared in anxiety in DS patients, suggesting distinct molecular mechanisms for anxiety in DS individuals. Functional overrepresentation analysis suggested that anxiety results from a complex interplay of genetic and environmental factors. Additionally, non-coding variants, particularly those proximal to splicing sites, play significant roles. Moreover, the variants associated with anxiety and other mental disorders are not uniquely distributed genome wide. Several loci, including 17q25, 16q23, 21q22, and 22q13, show greater weight in DS patients. Furthermore, 29 biomarkers containing recurrent anxiety-specific variants were identified to assist in the diagnosis of anxiety in the DS population. This pioneering study represents the first comprehensive exploration of anxiety disorders in DS utilizing WGS cohorts and advanced deep-learning AI models. The results indicate that anxiety disorder in DS patients has distinct molecular patterns from other mental disorders. The insights gained from our research offer valuable understanding of underlying mechanisms and hold promise for enhancing clinical diagnosis and potentially guiding more effective intervention strategies in this vulnerable population.

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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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