针对有神经发育和精神疾病遗传风险的儿童的综合临床方法:跨学科合作和研究基础设施。

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Jane Summers, Danielle Baribeau, Polina Perlman, Ny Hoang, Sunny Cui, Aneta Krakowski, Patricia Ambrozewicz, Ariel Ho, Thanuja Selvanayagam, Kinga A Sándor-Bajusz, Katrina Palad, Nishi Patel, Sarah McGaughey, Louise Gallagher, Stephen W Scherer, Peter Szatmari, Jacob Vorstman
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引用次数: 0

摘要

背景:在接受先天性差异检测的幼儿中发现的致病基因变异中,有相当一部分与神经发育性精神障碍(NPD)有关。在这个日益增长的群体中,遗传诊断往往先于可诊断的发育问题出现。在此,我们介绍了 DAGSY(易受遗传影响青少年的发育评估),这是一家新型的跨学科 "遗传诊断先行 "诊所,整合了精神科、心理科和遗传科的专业知识,并报告了我们的初步观察结果以及来自家庭和转诊临床医生的反馈意见:我们检索了 2018 年至 2022 年期间在 DAGSY 就诊的儿童的转诊来源和适应症、遗传和 NPD 诊断及建议数据。通过调查,我们获得了 20 个家庭和 11 名转诊临床医生的反馈:在此期间,159 名儿童(平均年龄 10.2 岁,57.2% 为男性)完成了跨学科(精神病学、心理学、遗传咨询)DAGSY 评估。其中 69.8% 患有致病性微缺失或微重复,21.5% 患有序列变异,4.4% 患有染色体紊乱,4.4% 患有意义不明的变异,但有新的致病证据。每 4 名儿童中就有 1 名之前未确诊过 NPD,转介到 DAGSY 的动机仅仅是他们的遗传易感性。经过评估后,76.7%的儿童至少接受了一项新的NPD诊断,其中最常见的是智力障碍(24.5%)、焦虑(20.7%)、自闭症谱系(18.9%)和特殊学习障碍(16.4%)。对我们的调查做出回应的家庭和临床医生都表示满意,但也强调了一些可能需要改进的地方:结论:DAGSY 解决了临床上尚未满足的需求,即发现儿童的基因变异会增加患 NPD 的可能性,并为该领域的研究提供了一个重要平台。DAGSY 可以作为整合儿童精神病学、心理学和遗传学的跨学科诊所的典范,满足这一新兴人群的临床和研究需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
An integrated clinical approach to children at genetic risk for neurodevelopmental and psychiatric conditions: interdisciplinary collaboration and research infrastructure.

Background: A sizeable proportion of pathogenic genetic variants identified in young children tested for congenital differences are associated with neurodevelopmental psychiatric disorders (NPD). In this growing group, a genetic diagnosis often precedes the emergence of diagnosable developmental concerns. Here, we describe DAGSY (Developmental Assessment of Genetically Susceptible Youth), a novel interdisciplinary 'genetic-diagnosis-first' clinic integrating psychiatric, psychological and genetic expertise, and report our first observations and feedback from families and referring clinicians.

Methods: We retrieved data on referral sources and indications, genetic and NPD diagnoses and recommendations for children seen at DAGSY between 2018 and 2022. Through a survey, we obtained feedback from twenty families and eleven referring clinicians.

Results: 159 children (mean age 10.2 years, 57.2% males) completed an interdisciplinary (psychiatry, psychology, genetic counselling) DAGSY assessment during this period. Of these, 69.8% had a pathogenic microdeletion or microduplication, 21.5% a sequence-level variant, 4.4% a chromosomal disorder, and 4.4% a variant of unknown significance with emerging evidence of pathogenicity. One in four children did not have a prior NPD diagnosis, and referral to DAGSY was motivated by their genetic vulnerability alone. Following assessment, 76.7% received at least one new NPD diagnosis, most frequently intellectual disability (24.5%), anxiety (20.7%), autism spectrum (18.9%) and specific learning (16.4%) disorder. Both families and clinicians responding to our survey expressed satisfaction, but also highlighted some areas for potential improvement.

Conclusions: DAGSY addresses an unmet clinical need for children identified with genetic variants that confer increased vulnerability for NPD and provides a crucial platform for research in this area. DAGSY can serve as a model for interdisciplinary clinics integrating child psychiatry, psychology and genetics, addressing both clinical and research needs for this emerging population.

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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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