Atypical Late Neurodevelopment in Autism: A Longitudinal MRI and DTI Study

自闭症的非典型晚期神经发育：纵向 MRI 和 DTI 研究

• 批准号: 7657468
• 负责人: JANET Elizabeth LAINHART
• 金额: $ 50.34万
• 依托单位: UNIVERSITY OF UTAH
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-08-01 至 2012-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7657468
• 关键词: 2 year old; 3 year old; 6 year old; Adult; Affect; Age; Age-Years; Anisotropy; Autistic Disorder; Base of the Brain; Brain; Brain region; Characteristics; Child; Childhood; Clinical; Clinical Data; Cognitive; Collaborations; Collection; Corpus Callosum; Data; Data Collection; Data Set; Development; Developmental Process; Diffusion; Diffusion Magnetic Resonance Imaging; Disease; Environmental Risk Factor; Fiber; Funding; Genes; Gray unit of radiation dose; Growth and Development function; Image; Impairment; Individual; Inferior frontal gyrus; Intervention; Language; Language Development; Life; Longitudinal Studies; Magnetic Resonance Imaging; Measures; Minor; Modeling; Pattern; Perception; Population; Preventive Intervention; Process; Radial; Research; Research Personnel; Sampling; Scanning; Sensory; Severities; Site; Staging; Structure; Temporal Lobe; Thalamic structure; Time; United States National Institutes of Health; Universities; Utah; Wisconsin; Work; base; brain behavior; brain volume; case control; clinical phenotype; cohort; computerized data processing; disability; frontal lobe; functional outcomes; gray matter; improved; information processing; interest; male; morphometry; neurodevelopment; neuroimaging; neuropathology; neuropsychological; phonology; postnatal; processing speed; programs; time use; white matter

DESCRIPTION (provided by applicant): In addition to efforts to describe the earliest signs of autism, it is critical to continue efforts to understand the brain-basis of autism, how it changes over time, and how it is related to the changing manifestations of the disorder in children and adults. The population of already-affected individuals with autism is huge and growing. It has become clear that autism in these individuals is a dynamic disorder and that a sizeable proportion of affected individuals worsen rather than improve as they grow older. Individuals whose impairment does not worsen over time live with stable but significant lifelong disability. The objective of this research is to understand longitudinal brain mechanisms from childhood into adulthood in autism and how dynamic brain and clinical phenotype changes are related. This research will result in new information important for the development of new treatments and secondary and tertiary preventive interventions. The specific aims of this project are to collect time 3 and time 4 longitudinal structural and diffusion tensor neuroimaging at 3 Telsa along with clinical and neuropsychological data on a large cohort of children and adults with autism and typically developing individuals. The collection of time 1 and time 2 data was funded by the NIH Collaborative Program of Excellence in Autism. This is a case-control longitudinal study of the original cohort of 100 males with autism and 72 matched normal controls. Subjects in the cohort are equally divided into 4 age-bins. At time 1 they were 3-6, 7-11, 12-17, and 18-35 years of age. At time 2 they were 2 years older. At times 3 and 4 they will be 4 and 6 years older. 3 Telsa structural and diffusion tensor imaging data were collected at time 1 and time 2 and will be collected at time 3 and 4 on the single, same scanner used for time 1 and 2. The 3 major and minor eigenvalues and eigenvectors are determined and fractional anisotropy, mean diffusivity, and axial and radial diffusivity calculated for quantitative assessment of white matter integrity. Region of interests and whole-brain voxel-based analyses of both structural and diffusion tensor imaging data are performed, along with tractography. Detailed clinical and neuropsychological data are collected on all subjects and dynamic brain-behavior relationships studied. This project is a collaborative effort between the University of Utah, where all subjects are ascertained, assessed, and scanned, the University of Wisconsin, where all diffusion tensor imaging data are processed and analyzed, and Brigham Young University where all structural data are processed and analyzed. This collaborative group has been effectively and productively working together on this longitudinal study since 2002.

描述（由申请人提供）：除了努力描述自闭症的最早迹象外，继续努力了解自闭症的大脑基础，它如何随着时间的推移而变化，以及它如何与儿童和成人疾病的变化表现相关，这一点至关重要。已经受影响的自闭症患者数量巨大，而且还在不断增长。很明显，这些人的自闭症是一种动态障碍，随着年龄的增长，相当一部分受影响的人会恶化而不是改善。损伤不随时间恶化的个人生活在稳定但严重的终身残疾中。本研究的目的是了解自闭症儿童到成年的纵向脑机制，以及动态脑和临床表型变化之间的关系。这项研究将为开发新的治疗方法以及二级和三级预防干预措施提供重要的新信息。该项目的具体目标是收集时间3和时间4纵向结构和弥散张量神经成像在3 Telsa沿着与临床和神经心理学数据的一个大队列的儿童和成人自闭症和典型的发展中国家的个人。时间1和时间2数据的收集由NIH自闭症卓越合作计划资助。这是一项病例对照纵向研究，研究对象为100名男性自闭症患者和72名匹配的正常对照。将队列中的受试者平均分为4个年龄组。在时间1，他们的年龄为3-6岁、7-11岁、12-17岁和18-35岁。在第二次的时候，他们大了两岁。在第3次和第4次，他们将分别大4岁和6岁。3在时间1和时间2收集Telsa结构和弥散张量成像数据，并将在时间3和4在用于时间1和2的单个相同扫描仪上收集。确定了3个主要和次要特征值和特征向量，并计算了分数各向异性、平均扩散率以及轴向和径向扩散率，用于白色物质完整性的定量评估。感兴趣的区域和全脑体素为基础的分析结构和扩散张量成像数据进行，沿着与纤维束成像。详细的临床和神经心理学数据收集所有科目和动态的大脑行为关系的研究。该项目是犹他州大学、威斯康星州大学和杨百翰大学之间的合作成果，在犹他州，所有受试者都被确定、评估和扫描，在威斯康星州，所有扩散张量成像数据都被处理和分析，在杨百翰大学，所有结构数据都被处理和分析。自2002年以来，该合作小组一直在有效和富有成效地共同开展这项纵向研究。