A familial modeling framework for advancing precision medicine for children with neuropsychiatric disorders.

IF 3.8 2区 医学 Q1 CLINICAL NEUROLOGY
Jennifer L Bruno, Jacob Joseph Merrin, S M Hadi Hosseini, Tamar Green
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引用次数: 0

Abstract

Aim: To provide individualized estimates of expected child neuropsychiatric and neuroanatomical outcomes by using parent cognitive and behavioral traits in a predictive framework.

Method: Predictive modeling was applied to 52 families of children with Noonan syndrome, a neurogenetic syndrome affecting the Ras/mitogen-activated protein kinase (MAPK) pathway.

Results: Parent cognition (specifically visuospatial and motor abilities), depression, anxiety, and attention-deficit/hyperactivity disorder symptoms were significantly associated with child outcomes in these domains. Parent cognition was also significantly associated with child neuroanatomical variability. The middle temporal cortex was weighted strongly in the model predicting child neuroanatomy and not identified in previous work, but was correlated with parent cognition, suggesting a larger familial effect in this region.

Interpretation: Using parent traits provides a more individualized estimate of expected child cognitive, behavioral, and neuroanatomical outcomes. Understanding how parent traits influence neuroanatomical outcomes helps to further a mechanistic understanding of the impact of Ras/MAPK on neurodevelopmental outcomes. Further refinement of predictive modeling to estimate individualized child outcomes will advance a precision medicine approach to treating Noonan syndrome, other neurogenetic syndromes, and neuropsychiatric disorders more broadly.

推进儿童神经精神疾病精准医学的家族性建模框架。
目的:通过在预测框架中使用父母的认知和行为特征,提供预期儿童神经精神和神经解剖学结果的个性化估计。方法:对52例影响Ras/丝裂原活化蛋白激酶(MAPK)通路的神经遗传综合征Noonan综合征患儿家庭进行预测建模。结果:父母的认知(特别是视觉空间和运动能力)、抑郁、焦虑和注意力缺陷/多动障碍症状与这些领域的儿童结局显著相关。父母的认知也与儿童的神经解剖学变异显著相关。中颞叶皮层在预测儿童神经解剖学的模型中权重很大,在以前的研究中没有发现,但与父母的认知相关,表明该区域存在更大的家族效应。解释:使用父母的特征提供了对预期儿童认知、行为和神经解剖学结果的更个性化的估计。了解亲本性状如何影响神经解剖学结果有助于进一步了解Ras/MAPK对神经发育结果影响的机制。进一步完善预测模型以估计个体化儿童的预后,将推动精准医学方法更广泛地治疗努南综合征、其他神经遗传综合征和神经精神疾病。
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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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