Using team-based precision medicine to advance understanding of rare genetic brain disorders.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Steven U Walkley, Sophie Molholm, Bryen Jordan, Robert W Marion, Melissa Wasserstein
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引用次数: 0

Abstract

We describe a multidisciplinary teamwork approach known as "Operation IDD Gene Team" developed by the Rose F. Kennedy Intellectual and Developmental Disabilities Research Center (RFK IDDRC) at the Albert Einstein College of Medicine. This initiative brings families affected by rare genetic diseases that cause intellectual and developmental disability together with physicians, basic scientists, and their trainees. At team meetings, family members share their child's medical and personal history, physicians describe the broader clinical consequences of the condition, and scientists provide accessible tutorials focused on the fundamental biology of relevant genes. When appropriate, possible treatment approaches are also discussed. The outcomes of team meetings have been overwhelmingly positive, with families not only expressing deep gratitude, but also becoming empowered to establish foundations dedicated to their child's specific condition. Physicians, and in particular the scientists and their trainees, have gained a deeper understanding of challenges faced by affected families, broadening their perspective on how their research can extend beyond the laboratory. Remarkably, research by the scientists following the Gene Team meetings have often included focus on the actual gene variants exhibited by the participating children. As these investigations progress and newly created foundations expand their efforts, national as well as international collaborations are forged. These developments emphasize the importance of rare diseases as windows into previously unexplored molecular and cellular processes, which can offer fresh insights into both normal function as well as more common diseases. Elucidating the mechanisms of and treatments for rare and ultra-rare diseases thus has benefits for all involved-families, physicians, and scientists and their trainees, as well as the broader medical community. While the RFK IDDRC's Operation IDD Gene Team program has focused on intellectual disabilities affecting children, we believe it has the potential to be applied to rare genetic diseases impacting individuals of any age and encompassing a wide variety of developmental disorders affecting multiple organ systems.

利用基于团队的精准医疗,增进对罕见遗传性脑部疾病的了解。
我们介绍了阿尔伯特-爱因斯坦医学院罗斯-肯尼迪智力和发育障碍研究中心(Rose F. Kennedy Intellectual and Developmental Disabilities Research Center,RFK IDDRC)开发的一种名为 "IDD 基因小组行动 "的多学科团队合作方法。这项计划将受罕见遗传病(导致智力和发育障碍)影响的家庭与医生、基础科学家及其受训人员聚集在一起。在团队会议上,家庭成员分享他们孩子的病史和个人经历,医生描述病情的广泛临床后果,而科学家则提供以相关基因的基础生物学为重点的通俗易懂的教程。在适当的时候,还会讨论可能的治疗方法。团队会议取得了非常积极的成果,家属们不仅深表感谢,而且有能力建立专门针对其子女特定病症的基金会。医生们,尤其是科学家和他们的受训人员,对受影响家庭所面临的挑战有了更深入的了解,从而拓宽了他们的视野,知道他们的研究如何能够延伸到实验室之外。值得注意的是,科学家们在基因小组会议后开展的研究往往包括对参与研究的儿童所表现出的实际基因变异的关注。随着这些调查的进展和新成立基金会的扩大,国内和国际合作也在不断加强。这些进展强调了罕见病的重要性,因为罕见病是了解以前未探索的分子和细胞过程的窗口,可以为正常功能和更常见的疾病提供新的见解。因此,阐明罕见病和超罕见病的发病机制和治疗方法对所有相关人员--家庭、医生、科学家及其受训人员以及更广泛的医学界都有好处。虽然肯尼迪国际残疾研究中心的 "IDD 基因小组行动 "计划侧重于影响儿童的智力残疾,但我们相信它有潜力应用于影响任何年龄段的人的罕见遗传疾病,包括影响多个器官系统的各种发育障碍。
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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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