Intervention-induced plasticity of flexibility and learning mechanisms in ASD

干预引起的自闭症谱系障碍灵活性和学习机制的可塑性

• 批准号: 10454197
• 负责人: LAUREN KENWORTHY
• 金额: $ 20.26万
• 依托单位: CHILDREN'S RESEARCH INSTITUTE
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-07-21 至 2026-05-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10454197
• 关键词: 18 year old; Adaptive Behaviors; Address; Adolescence; Attention; Behavior; Behavioral; Biological Markers; Brain; Canis familiaris; Categories; Child; Clinical; Cognitive; Cognitive Therapy; Computer Models; Coupled; Development; District of Columbia; Effectiveness of Interventions; Enrollment; Environment; Executive Dysfunction; Exhibits; Feedback; Functional Magnetic Resonance Imaging; Generations; Heterogeneity; Impairment; Individual; Individual Differences; Infrastructure; Intellectual and Developmental Disabilities Research Centers; Intelligence; Intervention; Investigation; Knowledge; Learning; Light; Link; Medial; Memory; Mental Health; Methodology; Modeling; Outcome; Outcome Measure; Performance; Prediction of Response to Therapy; Prefrontal Cortex; Recording of previous events; Research Personnel; Resources; Rest; Roter; Specificity; Temporal Lobe; Testing; Time; Treatment outcome; Universities; Youth; adolescent with autism spectrum disorder; autism spectrum disorder; autistic children; base; behavior measurement; behavioral response; bench to bedside; case control; comorbidity; design; executive function; experience; flexibility; improved; individual variation; intervention effect; neural correlate; neurobehavioral; neuroimaging; neuromechanism; novel; personalized medicine; prototype; relating to nervous system; response; skills; social; social skills; success; transfer learning; treatment response

PROJECT SUMMARY This exploratory project between CNH and Georgetown University leverages the DC-IDDRC infrastructure and its Neuroimaging, Neurobehavioral and Clinical Translational Cores to test mechanistic hypotheses about individual differences in the ability to transfer learned knowledge to novel settings in Autism Spectrum Disorders (ASD). The history of ASD intervention is rife with poor real-world outcomes and high heterogeneity in generalization success (1). One known contributing factor is executive dysfunction, particularly behavioral inflexibility (2, 3). Understanding this nexus of learning and executive function (4) likely holds the key to resolving the generalization challenge in ASD, but it has received little attention. The proposed project aims to elucidate the association between learning and flexibility by testing whether intervening to promote flexible behavior in ASD changes learning and associated neural mechanisms. The scientific premise of the proposed study is that flexible use of learned concepts depends on generating prototypes, whereas learning tuned to individual exemplars promotes specificity (5, 6). Current models of concept learning (7) have used computational modeling of individual generalization performance and model-based functional magnetic resonance imaging (m-fMRI) to attribute prototype-generation to ventral medial prefrontal cortex (vmPFC) and exemplar-biased learning to the medial temporal lobes (MTL) (8). We propose that variability in prototype/exemplar learning mechanisms is associated with behavioral flexibility and explains differences in adaptive and treatment outcomes. We employ a longitudinal case-controlled design in 54 14-18 year old youth with ASD at 3 time-points 8 months apart, each including m-fMRI during category learning and behavioral measurement of executive and adaptive function. Aim 1 tests the hypothesis that individual variation in learning biases (prototype/exemplar) and their neural correlates predicts behavioral flexibility (Time1) and is stable over time (Time2). Aim 2 tests plasticity of learning mechanisms induced by a cognitive-behavioral intervention for flexibility (Unstuck-and-On-Target) that targets development of prototypical knowledge (9). Intervention will strengthen prototype learning, and associated vmPFC involvement will be associated with better behavioral response to intervention. Aim 3 tests hypothesis about intervention-induced plasticity of intrinsic functional connectivity. Stronger resting- state functional connectivity between MTL and vmPFC specifically and network connectivity of the MTL subsystem of the default mode network (10) will be associated with prototype learning and intervention response. Our approach is novel, methodologically in the use of individualized characterization of learning mechanisms, and theoretically in unifying learning and executive function to explain mechanisms of treatment response and heterogeneity in treatment outcome in ASD. Findings will inform larger investigations of personalized treatments for promoting adaptive behavior in ASD.

项目摘要 CNH和乔治敦大学之间的这个探索性项目利用DC-IDDRC 基础设施及其待测试的神经成像、神经行为和临床转化核心 关于将所学知识转移到新知识的能力的个体差异的机械假说 自闭症谱系障碍（ASD）ASD干预的历史充斥着糟糕的现实世界， 结果和高度异质性的推广成功（1）。一个已知的影响因素是行政 功能障碍，特别是行为能力（2，3）。理解学习和执行功能之间的关系 (4)可能是解决ASD泛化挑战的关键，但它很少受到关注。的 拟议的项目旨在通过测试是否 通过干预促进ASD患者的灵活行为改变了学习和相关的神经机制。 拟议研究的科学前提是，灵活使用学到的概念取决于生成 原型，而学习调整到个人范例促进特异性（5，6）。当前概念模型 学习（7）已经使用了个人泛化性能的计算建模和基于模型的 功能性磁共振成像（m-fMRI）将原型生成归因于腹内侧前额叶 皮层（vmPFC）和内侧颞叶（MTL）的样本偏向学习（8）。我们建议 原型/范例学习机制的可变性与行为灵活性相关， 解释了适应性和治疗结果的差异。我们采用纵向病例对照设计 在54名14-18岁ASD青少年中，在3个时间点间隔8个月，每个时间点在分类期间包括m-fMRI， 执行和适应功能的学习和行为测量。目标1检验假设， 学习偏差的个体差异（原型/范例）及其神经相关预测 行为灵活性（时间1），并随时间推移保持稳定（时间2）。目标2测试学习的可塑性 认知行为干预诱导的灵活性机制（Unstuck-and-On-Target）， 目标是发展原型知识（9）。干预将加强原型学习， 相关的vmPFC参与将与对干预的更好的行为反应相关。Aim 3测试 关于内在功能连接的干预诱导可塑性的假说。更强的休息- 具体说明MTL和vmPFC之间的功能连接以及MTL的网络连接 默认模式网络（10）的子系统将与原型学习和干预响应相关联。 我们的方法是新颖的，在方法论上使用个性化的学习机制， 在理论上统一学习和执行功能，以解释治疗反应的机制， ASD治疗结果的异质性。研究结果将为更大规模的个性化治疗研究提供信息 促进自闭症患者的适应行为