推进儿童神经精神疾病精准医学的家族性建模框架

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
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引用次数: 0

摘要

患有努南综合症的儿童会经历认知挑战和注意力缺陷/多动障碍(ADHD)、焦虑和抑郁的症状。儿童在大脑结构和功能上也存在差异。所有这些都归因于导致努南综合征的基因变化。然而,就儿童的症状水平而言,存在很大的可变性,这使得父母和临床医生很难预测儿童的结果并计划治疗。除了导致努南综合症的基因变化外,父母还与孩子分享遗传信息和经历。鉴于此,本研究利用父母的认知和行为特征来预测孩子的相应特征。结果表明,父母认知预测了儿童的认知。父母的抑郁、焦虑和多动症症状水平也能预测孩子在相应领域的表现。与不使用父母特征相比,利用父母特征可以更精确地预测相应的儿童结果。父母的认知也与孩子的大脑结构显著相关,这是用磁共振成像来测量的。由于大脑结构代表了大脑发育的累积效应,这一证据表明父母的认知会影响孩子的大脑发育。了解父母的特征是如何影响大脑发育的,将有助于梳理遗传和环境等共同因素的影响,以及努南综合征遗传变化等独特因素的影响。目前对患有努南综合症的儿童的护理采用了与治疗多动症等其他疾病相同的观察、等待方法。虽然通常不包括在诊断测试中,但测量父母特征是一种多维的、无创的方法,可以增加有关预期结果的信息,这对父母和临床医生很有用。使用父母特征的预测模型(利用统计数据预测结果)在其他疾病的临床中也可能有用,并且,在未来的研究中,该框架可以帮助推进精确医学方法,包括利用每个患者的信息进行个性化治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A familial modeling framework for advancing precision medicine for children with neuropsychiatric disorders

Children with Noonan syndrome experience cognitive challenges and symptoms of attention-deficit/hyperactivity disorder (ADHD), anxiety, and depression. Children also have differences in brain structure and function. All the above are attributed to the genetic changes that cause Noonan syndrome. Yet there is a great variability in terms of the level of a child's symptoms which makes it difficult for parents and clinicians to predict a child's outcome and plan treatment. Aside from the genetic changes causing Noonan syndrome, parents share genetic information and experiences with their children. Given this knowledge, the present study utilized parent cognitive and behavioural traits to predict a child's corresponding traits.

Results indicated that parent cognition predicted a child's cognition. A parent's level of depression, anxiety, and ADHD symptoms also predicted child outcomes in corresponding domains. Utilizing parent traits allowed for more precise prediction of corresponding child outcomes than when parent traits were not used. Parent cognition was also significantly associated with child's brain structure which was measured using magnetic resonance imaging. Since brain structure represents cumulative effects of brain development, this evidence suggests that a parent's cognition influences a child's brain development. Understanding how parent traits influence brain development will help tease apart the effects of shared factors such as genetics and environment, and unique factors such as Noonan syndrome genetic changes.

Current care for children with Noonan syndrome follows the same watchful, waiting approach used for other disorders like ADHD. While not typically included in diagnostic testing, measuring parent traits is a multidimensional, noninvasive method that can add information regarding expected outcomes that is useful for parents and clinicians. Predictive modeling (employing statistics to predict outcomes) using parent traits may also be useful clinically in other disorders and, with future research, this framework can help advance a precision medicine approach which involves individualized treatment utilizing information about each patient.

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来源期刊
CiteScore
7.80
自引率
13.20%
发文量
338
审稿时长
3-6 weeks
期刊介绍: Wiley-Blackwell is pleased to publish Developmental Medicine & Child Neurology (DMCN), a Mac Keith Press publication and official journal of the American Academy for Cerebral Palsy and Developmental Medicine (AACPDM) and the British Paediatric Neurology Association (BPNA). For over 50 years, DMCN has defined the field of paediatric neurology and neurodisability and is one of the world’s leading journals in the whole field of paediatrics. DMCN disseminates a range of information worldwide to improve the lives of disabled children and their families. The high quality of published articles is maintained by expert review, including independent statistical assessment, before acceptance.
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