A neuroimaging study of twin pairs with autism

自闭症双胞胎的神经影像学研究

• 批准号: 8205000
• 负责人: ANTONIO HARDAN
• 金额: $ 62.56万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-02-01 至 2013-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8205000
• 关键词: Address; Adult; Affect; Age; Amygdaloid structure; Anatomy; Anisotropy; Area; Autistic Disorder; Behavior; Behavioral; Biological; Brain; Brain imaging; Brain region; California; Cerebrum; Characteristics; Chemistry; Child; Clinical; Cognitive; Complex; Control Groups; Corpus Callosum; Data; Dependence; Development; Diagnosis; Diagnostic; Diffusion; Diffusion Magnetic Resonance Imaging; Disabled Persons; Disease; Employment; Environmental Risk Factor; Functional disorder; Funding; Gender; Genetic; Genetic Risk; Goals; Gray unit of radiation dose; Health; Heritability; Image; Impairment; Individual; Intelligence; Interview; Investigation; Language; Lead; Life; Literature; Magnetic Resonance Imaging; Matched Group; Measures; Metabolic; Mind; N-acetylaspartate; National Institute of Mental Health; National Institute of Neurological Disorders and Stroke; Nature; Neurobiology; Neurodevelopmental Disorder; Outcome; Outcome Study; Parietal; Participant; Pathway interactions; Pattern; Prevalence; Procedures; Protons; Recruitment Activity; Regression Analysis; Relative (related person); Reporting; Research; Resolution; Sampling; Scanning; Schedule; Sensory Process; Siblings; Social Characteristics; Socioeconomic Status; Spectrum Analysis; Stereotyped Behavior; Stereotyping; Structure; Subgroup; Symptoms; Thalamic structure; Therapeutic; Thick; Time; Twin Multiple Birth; Twin Studies; Update; Variant; autism spectrum disorder; base; behavior measurement; brain behavior; cognitive function; design; endophenotype; executive function; genetic epidemiology; gray matter; handicapping condition; improved; innovation; interest; network dysfunction; neurochemistry; neuroimaging; non-genetic; population based; proband; sex; social; social cognition; social communication; theories; therapeutic target; trait; white matter

DESCRIPTION (provided by applicant): Autism is a severe neurodevelopmental disorder characterized by marked social and communication deficits, restricted and stereotyped patterns of behaviors and interests with evidence supporting its neurobiologic and polygenic basis. The proposed study will build on an ongoing NIMH-funded study (R01 MH 067005 "A population-based twin study of autism in California" PI: Joachim Hallmayer). The existence of this population-based study of twins, with at least one twin with autism, will provide unprecedented opportunities to examine the relative impact of genetic and nongenetics factors on brain anatomy and chemistry in autism. Specifically, from this sample of more than 120 twin pairs who completed the genetic study to date, we will randomly recruit 80 same-sex autism twin pairs, 40 MZ and 40 DZ. We will also recruit 40 typically developing same-sex twin pair controls, 20 MZ and 20 DZ, group-matched to the sample comprised by the 80 autistic (twin) probands for age, gender, and socioeconomic status. High resolution anatomical, diffusion tensor and proton spectroscopy scans will be obtained from all participants. All new data collected in this study will be evaluated in the context of extensive cognitive and behavioral measures available from the ongoing NIMH study described above. We also will collect additional clinical measures at the time of the proposed imaging investigation to provide more specific covariates for neuroanatomical and neurochemical variables. The overarching goal is to develop a better understanding of linkages among clinical features and neurobiological measures in individuals affected by autism, thus allowing the identification of clinical or biological endophenotypes that will lead to a better characterization and understanding of this disorder. Twin studies in autism are particularly informative for examining the relative contribution of genetic and environmental risk factors to neurobiologic variations observed in this disorder. Improving our understanding of the neurobiology of autism and brain behavior correlations will help in the development of better procedures for predicting outcome and the design and implementation of more targeted therapeutic approaches. PUBLIC HEALTH RELEVANCE: Autism and autism spectrum disorders are very heterogeneous and disabling conditions with recent estimates suggesting that the prevalence of this class of disorders may be considerably higher than previously thought (NINDS, 1983; Fombonne, 2003). Adult outcome studies indicate that about two thirds of autistic adults remain severely handicapped and live in complete dependence or semi-dependence, with only 1 to 2 percent acquiring a normal and independent status with gainful employment, and 5 to 20 percent achieving a borderline normal status (Young et al., 1989). Therefore, the quest continues to identify innovative strategies that will allow us to better understand the neurobiology of this disorder. Twin studies in autism are very informative since they facilitate the examination of the relative contribution of genetic and environmental risk factors to the neurobiologic changes observed in this disorder. A better understanding of the pathophysiology of autism will be instrumental in the development of effective therapeutic strategies that aim at targeting the core symptoms of social and communication deficits.

描述(申请人提供)：自闭症是一种严重的神经发育障碍，其特征是明显的社交和沟通障碍，行为和兴趣的受限和刻板印象，证据支持其神经生物学和多基因基础。这项拟议的研究将建立在NIMH资助的一项正在进行的研究(R01 MH 067005“加州自闭症的基于人群的双胞胎研究”PI：Joachim Hallmayer)的基础上。这项基于人群的双胞胎研究至少有一人患有自闭症，这一研究的存在将提供前所未有的机会，来研究遗传和非遗传因素对自闭症患者大脑解剖和化学的相对影响。具体地说，从到目前为止完成基因研究的120多对双胞胎中，我们将随机招募80对同性自闭症双胞胎，40名MZ和40名DZ。我们还将招募40名典型的同性双胞胎对照，20名MZ和20名DZ，与80名自闭症(双胞胎)先证者的年龄、性别和社会经济地位的样本进行分组匹配。将从所有参与者那里获得高分辨率的解剖、扩散张量和质子光谱扫描。在这项研究中收集的所有新数据将在上述正在进行的NIMH研究中可获得的广泛认知和行为测量的背景下进行评估。我们还将在拟议的影像研究时收集额外的临床措施，以提供神经解剖学和神经化学变量的更具体的协变量。总体目标是更好地了解自闭症患者的临床特征和神经生物学措施之间的联系，从而能够确定临床或生物内表型，从而更好地描述和理解这种疾病。自闭症的双胞胎研究对于检验遗传和环境风险因素对这种疾病中观察到的神经生物学变化的相对贡献特别有意义。提高我们对自闭症的神经生物学和大脑行为相关性的理解，将有助于开发更好的程序来预测结果，并设计和实施更有针对性的治疗方法。公共卫生相关性：自闭症和自闭症谱系障碍是非常不同的和致残的疾病，最近的估计表明，这类障碍的患病率可能比之前认为的要高得多(NINDS，1983；Fombonne，2003)。成人结局研究表明，大约三分之二的自闭症成年人仍然严重残疾，生活在完全依赖或半依赖中，只有1%到2%的人获得了正常和独立的状态，并获得了有报酬的工作，5%到20%的人达到了接近正常的状态(Young等人，1989)。因此，这项探索将继续确定创新的策略，使我们能够更好地了解这种疾病的神经生物学。自闭症的双胞胎研究非常有用，因为它们有助于检查遗传和环境风险因素对这种疾病中观察到的神经生物学变化的相对贡献。更好地了解自闭症的病理生理学将有助于制定有效的治疗策略，旨在针对社交和沟通障碍的核心症状。