Characterizing mechanistic heterogeneity across ADHD and Autism

描述多动症和自闭症的机制异质性

• 批准号: 9272012
• 负责人: Damien A Fair
• 金额: $ 38.99万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-08-06 至 2018-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9272012
• 关键词: Address; Affect; Amygdaloid structure; Ants; Attention deficit hyperactivity disorder; Autistic Disorder; Behavior; Behavioral; Bilateral; Biological; Brain; Brain imaging; Child; Child Psychiatry; Classification; Clinical; Communities; Complement; Corpus Callosum; Corpus striatum structure; Data; Detection; Development; Developmental Disabilities; Diagnosis; Diffusion Magnetic Resonance Imaging; Disease; Early identification; Etiology; Face; Fusiform gyrus; Future; Genetic; Heterogeneity; Imaging Techniques; Impairment; Impulsivity; Inferior; Investigation; Knowledge; Life; Machine Learning; Magnetic Resonance Imaging; Measures; Mental disorders; Methods; Modality; National Institute of Mental Health; Nature; Neurobiology; Neurodevelopmental Disorder; Output; Parietal; Patients; Pattern; Performance; Physiology; Prevention; Psychometrics; Research Domain Criteria; Rest; Short-Term Memory; Speed; Strategic Planning; Structure; Structure of superior temporal sulcus; Surveys; Syndrome; System; Therapeutic; Work; Youth; autism spectrum disorder; base; biological heterogeneity; biosignature; computerized tools; cost; developmental disease; early onset; endophenotype; executive function; graph theory; improved; innovation; multimodality; novel strategies; response; study population; translational study

DESCRIPTION (provided by applicant): Progress in establishing the etiology of psychiatric illness is limited by the absence of objective biological measures able to detect and discriminate between disorders. This problem is particularly important in developmental disorders, where early identification could eventually assist in prevention of lifelong impairments. The two earlies onsets, most common and costly developmental disorders in child psychiatry are attention deficit hyperactivity disorder (ADHD) and Autism spectrum disorders (ASD). A recent 2011 study, surveying the years 1997-2008, has now verified that 1 in 6 children have a developmental disability, a 17% increase over the past decade driven largely by increases in ASD and ADHD. These developments highlight the need for innovative approaches to address the underlying cause of these disorders. It is likely that the clinical heterogeneity and the imprecise nature of their nosological distinctions represent fundamentally confounding factors limiting a better understanding of their etiology, prevention, and treatment. Interestingly, an emerging observation regarding brain imaging in ASD and ADHD is that they often have the same atypical functional brain signatures. However, because these two syndromes are almost exclusively studied separately, it is difficult to determine atypical brain function that is common compared to what is distinct for each disorder. If we are to improve our understanding regarding the underlying etiology of these disorders, it will be necessary to study these populations simultaneously. With that said, simply comparing groups of children based on their DSM diagnosis is unlikely to suffice. The behavioral and biological heterogeneity within each syndrome further complicates the meaning of any given group difference found in brain imaging. Thus, progress in our understanding requires not only examining these disorders in the same studies, but also identifying how brain signatures relate to distinct behavioral components (i.e., endophenotypes) that span the syndromes. Under this context, and consistent with NIMH's new strategic plan, Strategy 1.4 (also see RDoC), the current proposal aims to use resting state functional connectivity MRI (rs-fcMRI) and structural connectivity (DTI) to identify brain signatures that correspond to fundamental behavioral components (executive, facial recognition, and affect recognition) found in ADHD and/or ASD. We also aim to develop integrated, multimodal sub-classifications (i.e. neurotypes) or "biosignatures" of these disorders with computational tools that include Graph Theory and support vector machine (SVM) based pattern classification. The potential impact of the proposed mechanistic categorization on future functional, genetic, treatment, and other translational studies of ADHD and ASD are substantial.

描述（由申请人提供）：由于缺乏能够检测和区分疾病的客观生物学指标，在确定精神疾病病因方面的进展受到限制。这个问题在发育障碍中尤其重要，早期识别最终可能有助于预防终身障碍。在儿童精神病学中，最常见和最昂贵的两种早期发病的发育障碍是注意缺陷多动障碍（ADHD）和自闭症谱系障碍（ASD）。最近2011年的一项研究调查了1997-2008年，现已证实，六分之一的儿童患有发育障碍，在过去十年中增加了17%，主要是由于ASD和ADHD的增加。这些事态发展突出表明，需要采取创新方法来解决这些疾病的根本原因。很可能是临床异质性和疾病分类学差异的不精确性从根本上代表了限制更好地了解其病因、预防和治疗的混杂因素。 有趣的是，关于ASD和ADHD的大脑成像的一个新发现是，它们通常具有相同的非典型功能性大脑特征。然而，由于这两种综合征几乎完全是单独研究的，因此很难确定与每种疾病不同的脑功能相比常见的非典型脑功能。如果我们要提高我们对这些疾病的潜在病因的理解，有必要同时研究这些人群。话虽如此，仅仅根据DSM诊断来比较儿童群体是不够的。每种综合征的行为和生物学异质性进一步复杂化了脑成像中发现的任何给定组差异的意义。因此，我们理解的进步不仅需要在相同的研究中检查这些疾病，而且还需要确定大脑特征如何与不同的行为成分（即，内表型），跨越综合征。 在这种情况下，并与NIMH的新战略计划，战略1.4（也见RDoC）一致，目前的提案旨在使用静息状态功能连接MRI（rs-fcMRI）和结构连接（DTI）来识别与ADHD和/或ASD中发现的基本行为成分（执行，面部识别和情感识别）相对应的大脑签名。我们的目标还包括开发集成的，多模式的子分类（即神经型）或“生物特征”，这些疾病的计算工具，包括图论和支持向量机（SVM）的模式分类。提出的机制分类对未来ADHD和ASD的功能，遗传，治疗和其他翻译研究的潜在影响是巨大的。