Neural and developmental trajectories of females with autism spectrum disorder
患有自闭症谱系障碍的女性的神经和发育轨迹
基本信息
- 批准号:10443473
- 负责人:
- 金额:$ 79.63万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2022
- 资助国家:美国
- 起止时间:2022-05-01 至 2027-02-28
- 项目状态:未结题
- 来源:
- 关键词:12 year old6 year oldAddressAgeAmygdaloid structureAreaAttention deficit hyperactivity disorderAttenuatedBehavioralBiological MarkersBrainBrain regionCaringDataDetectionDevelopmentDiagnosisDiagnosticDiseaseEmotionalEnrollmentEtiologyExhibitsFemaleFeminizationGenderGeneral PopulationGoalsHyperactivityImpulsivityIndividualKnowledgeLeadLiteratureLongevityLongitudinal StudiesLongitudinal cohortMasculineMedicineModelingParticipantPatternPrevalenceProtocols documentationPsychopathologyResearchRisk FactorsSamplingSampling StudiesSelf-Injurious BehaviorSex DifferencesStrategic PlanningSymptomsSystemTestingTheoretical modelTimeUnited States Dept. of Health and Human ServicesUnited States National Institutes of HealthWomanWomen&aposs Healthattenuationautism spectrum disorderautisticbasebehavioral phenotypingboyscohortdisorder riskearly childhoodemotion dysregulationemotion regulationethnic minority populationexternalizing behaviorgirlsimaging studyinattentionindividuals with autism spectrum disorderinsightmalemiddle childhoodneuroimagingoptimal treatmentsoutcome predictionpeerphenomeprogramsprotective effectracial minorityrecruitrelating to nervous systemrestrictive repetitive behaviorsensorimotor systemserial imagingsextheories
项目摘要
Girls and women are understudied in autism spectrum disorder (ASD) research because study samples often
reflect the male predominance in ASD prevalence, with 3-4 boys diagnosed for every girl. Longitudinal imaging
studies with sufficient numbers of females are completely lacking. To address this important gap in knowledge,
we aim to evaluate brain and behavioral trajectories from early to middle childhood in a large, longitudinal
cohort of nearly 100 girls with autism. As the field moves towards identifying neural biomarkers for ASD risk
and predicting outcomes, it is critical to understand similarities and differences between males and females
with ASD across the lifespan. Another serious need is to better understand co-occurring psychiatric conditions
in females with ASD. It is well-recognized that individuals with autism have high rates of co-occurring
psychopathology, but little is known about early behavioral and neural risk factors that may be specific to girls.
As in so many other areas of medicine, the optimal treatment of girls and women with ASD will only emerge
when sex-related autism attributes and problems are adequately understood. In 2014, we established the Girls
with Autism – Neuroimaging of Development (GAIN) study, which increased representation of females with
ASD in a larger ongoing project called the Autism Phenome Project and followed a cohort of girls across three
time points from 2-6 years of age. With this application, we plan to conduct a fourth longitudinal time point in
GAIN participants during middle childhood (9-12 years of age). In addition, in order to increase generalizability
of findings, we plan to enroll new girls into the study with a focus on racial and ethnic minority groups that have
historically been under-represented. Newly enrolled girls will follow the same study protocols established by
the GAIN study and data will be combined. We propose the following aims: 1) To identify sex-specific neural
and behavioral patterns in girls with ASD in early and middle childhood. 2) To identify sex differences in neural
risk factors associated with symptoms of internalizing and externalizing psychopathology in middle childhood.
3) To characterize the emergence and impact of symptoms of attention deficit/hyperactivity disorder (ADHD) in
girls with ASD. Evaluating females with ASD is a cross-cutting goal that spans all objectives of the US
Department of Health & Human Services Interagency Autism Coordinating Committee and is also consistent
with the goals of the Trans-NIH Strategic Plan for Women’s Health Research.
女孩和妇女在自闭症谱系障碍 (ASD) 研究中的研究不足,因为研究样本经常
反映了自闭症谱系障碍患病率中男性占主导地位,每个女孩对应 3-4 个被诊断出的男孩。纵向成像
完全缺乏对足够数量的女性进行的研究。为了解决这一重要的知识差距,
我们的目标是在大型纵向研究中评估从幼儿期到中期的大脑和行为轨迹
近100名患有自闭症的女孩组成的队列。随着该领域朝着识别自闭症谱系障碍 (ASD) 风险的神经生物标志物方向发展
和预测结果,了解男性和女性之间的异同至关重要
患有 ASD 的整个生命周期。另一个迫切需要是更好地了解同时发生的精神疾病
患有 ASD 的女性。众所周知,患有自闭症的人有很高的共患率
精神病理学,但人们对女孩特有的早期行为和神经危险因素知之甚少。
与许多其他医学领域一样,患有自闭症谱系障碍的女孩和妇女的最佳治疗方法只会出现
当与性相关的自闭症属性和问题得到充分理解时。 2014年,我们成立了女孩
自闭症——发育神经影像(GAIN)研究,该研究增加了患有自闭症的女性的比例
自闭症谱系障碍 (ASD) 参与了一个更大的正在进行的项目,称为“自闭症现象组项目”,跟踪了一群跨越三个年龄段的女孩
时间点为2-6岁。通过此应用程序,我们计划在
吸引儿童中期(9-12 岁)的参与者。另外,为了增加普适性
根据调查结果,我们计划让新女孩参加这项研究,重点关注那些拥有
历史上代表性不足。新入学的女孩将遵循由
GAIN 研究和数据将被合并。我们提出以下目标:1)识别性别特异性神经元
以及患有自闭症谱系障碍的女孩在童年早期和中期的行为模式。 2)识别神经元的性别差异
与童年中期内化和外化精神病理学症状相关的危险因素。
3) 描述注意力缺陷/多动障碍 (ADHD) 症状的出现和影响
患有自闭症谱系障碍的女孩。评估患有自闭症谱系障碍的女性是一个跨领域目标,涵盖美国的所有目标
卫生与公众服务部机构间自闭症协调委员会也一致
与跨 NIH 女性健康研究战略计划的目标。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Christine Wu Nordahl其他文献
19.2 SEX DIFFERENCES IN AMYGDALA DEVELOPMENT IN AUTISM SPECTRUM DISORDER FROM EARLY TO MIDDLE CHILDHOOD
- DOI:
10.1016/j.jaac.2021.07.662 - 发表时间:
2021-10-01 - 期刊:
- 影响因子:
- 作者:
Christine Wu Nordahl - 通讯作者:
Christine Wu Nordahl
Correction: Video Game Use, Aggression, and Social Impairment in Adolescents with Autism Spectrum Disorder
- DOI:
10.1007/s10803-022-05694-w - 发表时间:
2022-07-29 - 期刊:
- 影响因子:2.800
- 作者:
Konnor Davis;Ana-Maria Iosif;Christine Wu Nordahl;Marjorie Solomon;Marie K. Krug - 通讯作者:
Marie K. Krug
Sex Differences in the Striatal Contributions to Longitudinal Fine Motor Development in Autistic Children
自闭症儿童纹状体对纵向精细运动发展的性别差异
- DOI:
10.1016/j.biopsych.2025.01.005 - 发表时间:
2025-06-15 - 期刊:
- 影响因子:9.000
- 作者:
Olivia Surgent;Derek S. Andrews;Joshua K. Lee;Joseph Boyle;Andrew Dakopolos;Meghan Miller;Sally Ozonoff;Sally J. Rogers;Marjorie Solomon;David G. Amaral;Christine Wu Nordahl - 通讯作者:
Christine Wu Nordahl
Erratum: Sex differences in the corpus callosum in preschool-aged children with autism spectrum disorder
- DOI:
10.1186/s13229-015-0030-3 - 发表时间:
2015-06-20 - 期刊:
- 影响因子:5.500
- 作者:
Christine Wu Nordahl;Ana-Maria Iosif;Gregory S Young;Lee Michael Perry;Robert Dougherty;Aaron Lee;Deana Li;Michael H Buonocore;Tony Simon;Sally Rogers;Brian Wandell;David G Amaral - 通讯作者:
David G Amaral
Christine Wu Nordahl的其他文献
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{{ truncateString('Christine Wu Nordahl', 18)}}的其他基金
Neural and developmental trajectories of females with autism spectrum disorder
患有自闭症谱系障碍的女性的神经和发育轨迹
- 批准号:
10614560 - 财政年份:2022
- 资助金额:
$ 79.63万 - 项目类别:
Behavioral and Neurobiological Phenotyping of ASD with Megalencephaly
自闭症谱系障碍(ASD)伴巨脑畸形的行为和神经生物学表型
- 批准号:
10238007 - 财政年份:2017
- 资助金额:
$ 79.63万 - 项目类别:
Neural Phenotypes of Females with Autism Spectrum Disorder
患有自闭症谱系障碍的女性的神经表型
- 批准号:
8749078 - 财政年份:2014
- 资助金额:
$ 79.63万 - 项目类别:
Neural Phenotypes of Females with Autism Spectrum Disorder
患有自闭症谱系障碍的女性的神经表型
- 批准号:
9248812 - 财政年份:2014
- 资助金额:
$ 79.63万 - 项目类别:
Analyses of Brain Structure and Connectivity in Young Children with Autism
自闭症幼儿的大脑结构和连接性分析
- 批准号:
8519565 - 财政年份:2011
- 资助金额:
$ 79.63万 - 项目类别:
PROTEOMIC PROFILING OF INTEGRAL MEMBRANE PROTEIN TOPOLOGY
整体膜蛋白拓扑结构的蛋白质组学分析
- 批准号:
8365856 - 财政年份:2011
- 资助金额:
$ 79.63万 - 项目类别:
IDENTIFICATION OF HUMAN PROTEINS IN A MOUSE XENOGRAPH MODEL
小鼠异种模型中人类蛋白质的鉴定
- 批准号:
8365848 - 财政年份:2011
- 资助金额:
$ 79.63万 - 项目类别:
Analyses of Brain Structure and Connectivity in Young Children with Autism
自闭症幼儿的大脑结构和连接性分析
- 批准号:
8299854 - 财政年份:2011
- 资助金额:
$ 79.63万 - 项目类别:
Analyses of Brain Structure and Connectivity in Young Children with Autism
自闭症幼儿的大脑结构和连接性分析
- 批准号:
8320314 - 财政年份:2011
- 资助金额:
$ 79.63万 - 项目类别:
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