Neural and behavioral predictors of cognitive development and internalizing problems in adolescents with autism spectrum disorder
Neural and behavioral predictors of cognitive development and internalizing problems in adolescents with autism spectrum disorder
批准号:
10620645
负责人:
MARJORIE SOLOMON
金额:
$73.85万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
未结题
起止时间:
2014-09-11 至 2025-04-30
关键词:
AddressAdolescenceAdolescentAdultAgeAmygdaloid structureAnxietyAnxiety DisordersAwarenessBehaviorBehavioralBrain imagingCharacteristicsChildCognitionCognitiveComplexCorpus striatum structureCoupledDepressed moodDevelopmentDiseaseEarly identificationEmotionalEmotionsEpisodic memoryExhibitsFunctional Magnetic Resonance ImagingGrantHeterogeneityHippocampusIndividualIntellectual functioning disabilityInterviewInvestigationKnowledgeLongitudinal StudiesMeasurementMemoryMental DepressionMental disordersModelingMotivationNational Institute of Mental HealthOutcomeParentsPerformancePhenotypePilot ProjectsPsychopathologyQuestionnairesReportingRestSocial DevelopmentSocial FunctioningStrategic PlanningTestingTimeadolescent with autism spectrum disorderautism spectrum disorderautistic childrenbehavior predictionchild depressioncognitive abilitycognitive controlcognitive developmentcohortdepressive symptomsearly childhoodexperienceflexibilityimprovedmiddle childhoodneuralneural circuitneuroimagingphenomeprecision medicinepredictive modelingsocialsocial relationshipstherapy development
中文摘要
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英文摘要
ABSTRACT:
Adolescence is a period of strong cortical plasticity accompanied by significant changes in cognitive, social,
and adaptive functioning. Despite the promise characteristic of this period, it is also a time when social
relationships and emotion processing may intensify, and depression and other forms of psychopathology first
emerge. The lack of longitudinal studies of adolescents with autism spectrum disorder (ASD), coupled with the
disorder's heterogeneity, clouds our understanding of development during this complex period, and hinders
treatment development. We thus propose to extend our longitudinal investigation of children from the UC Davis
MIND Institute Autism Phenome Project cohort into adolescence. In Specific Aim #1, we predict aspects of
cognitive development in adolescents with ASD based on grant period studies. We hypothesize that ASD will
continue to exhibit at least three trajectories of intellectual functioning (IQ) -- a group with persistently below
average IQs (< 75) from early childhood through adolescence (Persistently Low or P-Low), a group with IQs <
75 in early childhood that increase by at least 1 standard deviation by adolescence (Positive Changers or
+CHG), and a group with persistently average or better IQs (>75) (Persistently High or P-High). We also
predict that preparatory cognitive control will continue to be comparable to TYP, but will be associated with
behavioral inflexibility; that all groups will exhibit comparable performance on aspects of episodic memory; and
that P-Low will show fewer negative emotional false memories. In Specific Aim #2, we examine social
awareness, motivation, and adaptive functioning in between middle childhood and adolescence in ASD. We
predict that +CHG will show improved social awareness and functioning compared to P-Low and P-High,
while all groups show declining social motivation, and that resting state functional magnetic resonance imaging
functional connectivity (FC) between the executive/cognitive control (ECN), default mode (DMN), and salience
(SN) networks will be predictive of adolescent social awareness and social functioning while social motivation
is predicted by concurrent engagement of the striatum. Specific Aim #3 investigates the emergence of
depression in ASD between middle childhood and adolescence. We test a prominent model predicting that
increased depression between middle childhood and adolescence will be more common in P-High and +CHG,
and will be associated with increased social awareness, greater retention of negative emotional memories, and
less flexible cognitive control. Additionally, we predict that during a well-validated task-based fMRI Sadness
Introspection Paradigm, functional connectivity between the ECN, DMN, SN, amygdala, and hippocampus
during sadness introspection will be associated with adolescent depression in P-High and +CHG. We also
predict that parent questionnaires, compared to gold standard clinician interviews, will under-report depression
in P-Low. This longitudinal examination of cognition, social functioning, and depression in adolescents with
ASD holds the potential to identify early markers of depression and more tailored precision medicine solutions.
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Components of Executive Control in Autism Spectrum Disorder: A Functional Magnetic Resonance Imaging Examination of Dual-Mechanism Accounts.
自闭症谱系障碍中执行控制的组成部分:双重力学帐户的功能磁共振成像检查。
DOI:
10.1016/j.bpsc.2020.11.008
发表时间:
2021-08
期刊:
Biological psychiatry. Cognitive neuroscience and neuroimaging
影响因子:
--
作者:
[Gordon A, Krug MK, Wulff R, Elliott MV, Hogeveen J, Lesh T, Carter C, Solomon M]
通讯作者:
Solomon M
Longitudinal Evaluation of Cerebral Growth Across Childhood in Boys and Girls With Autism Spectrum Disorder.
自闭症谱系障碍的男孩和女孩对童年整个儿童脑增长的纵向评估。
DOI:
10.1016/j.biopsych.2020.10.014
发表时间:
2021-09-01
期刊:
Biological psychiatry
影响因子:
10.6
作者:
[Lee JK, Andrews DS, Ozonoff S, Solomon M, Rogers S, Amaral DG, Nordahl CW]
通讯作者:
Nordahl CW
DOI:
10.1016/j.biopsych.2022.01.016
发表时间:
2022-06-01
期刊:
Biological psychiatry
影响因子:
10.6
作者:
[]
通讯作者:
DOI:
10.1080/23794925.2021.1923090
发表时间:
2022
期刊:
Evidence-based practice in child and adolescent mental health
影响因子:
--
作者:
[Winder-Patel B, Tudor ME, Kerns CM, Davis K, Nordahl CW, Amaral DG, Solomon M]
通讯作者:
Solomon M
DOI:
10.1002/aur.1884
发表时间:
2018
期刊:
Autism research : official journal of the International Society for Autism Research
影响因子:
--
作者:
[Solomon,Marjorie, Iosif,Ana-Maria, Reinhardt,VanessaP, Libero,LaurenE, Nordahl,ChristineW, Ozonoff,Sally, Rogers,SallyJ, Amaral,DavidG]
通讯作者:
Amaral,DavidG
共 21 条
Specifying and Treating the Anxiety Phenotype in Autism Spectrum Disorder
-
批准号:10238006
-
项目类别:
-
资助金额:$62.87万
-
财政年份:2017
-
负责人:MARJORIE SOLOMON
-
依托单位:
Neurodevelopment of cognitive control in autism: adolescence to young adulthood
-
批准号:9197344
-
项目类别:
-
资助金额:$60.67万
-
财政年份:2016
-
负责人:MARJORIE SOLOMON
-
依托单位:
Predictors of Cognitive Development in Autism Spectrum Disorder
-
批准号:8926469
-
项目类别:
-
资助金额:$50.46万
-
财政年份:2014
-
负责人:MARJORIE SOLOMON
-
依托单位:
Neural and behavioral predictors of cognitive development and internalizing problems in adolescents with autism spectrum disorder
-
批准号:10208691
-
项目类别:
-
资助金额:$73.6万
-
财政年份:2014
-
负责人:MARJORIE SOLOMON
-
依托单位:
Neural and behavioral predictors of cognitive development and internalizing problems in adolescents with autism spectrum disorder
-
批准号:10400906
-
项目类别:
-
资助金额:$73.94万
-
财政年份:2014
-
负责人:MARJORIE SOLOMON
-
依托单位:
Predictors of Cognitive Development in Autism Spectrum Disorder
-
批准号:8817161
-
项目类别:
-
资助金额:$55.76万
-
财政年份:2014
-
负责人:MARJORIE SOLOMON
-
依托单位:
The Neural Substrates of Higher-Level Learning in Autism
-
批准号:8426620
-
项目类别:
-
资助金额:$19.25万
-
财政年份:2012
-
负责人:MARJORIE SOLOMON
-
依托单位:
The Neural Substrates of Higher-Level Learning in Autism
-
批准号:8545902
-
项目类别:
-
资助金额:$22.18万
-
财政年份:2012
-
负责人:MARJORIE SOLOMON
-
依托单位:
Cognitive Control in Autism
-
批准号:7816843
-
项目类别:
-
资助金额:$14.98万
-
财政年份:2007
-
负责人:MARJORIE SOLOMON
-
依托单位:
Cognitive Control in Autism
-
批准号:7478707
-
项目类别:
-
资助金额:$14.43万
-
财政年份:2007
-
负责人:MARJORIE SOLOMON
-
依托单位:
Cognitive Control in Autism
-
批准号:7262097
-
项目类别:
-
资助金额:$14.16万
-
财政年份:2007
-
负责人:MARJORIE SOLOMON
-
依托单位:
Cognitive Control in Autism
-
批准号:8062293
-
项目类别:
-
资助金额:$15.26万
-
财政年份:2007
-
负责人:MARJORIE SOLOMON
-
依托单位:
Cognitive Control in Autism
-
批准号:7614538
-
项目类别:
-
资助金额:$14.7万
-
财政年份:2007
-
负责人:MARJORIE SOLOMON
-
依托单位:
Specifying and Treating the Anxiety Phenotype in Autism Spectrum Disorder
-
批准号:9388793
-
项目类别:
-
资助金额:$62.96万
-
财政年份:--
-
负责人:MARJORIE SOLOMON
-
依托单位:
Specifying and Treating the Anxiety Phenotype in Autism Spectrum Disorder
-
批准号:9761858
-
项目类别:
-
资助金额:$51.75万
-
财政年份:--
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负责人:MARJORIE SOLOMON
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依托单位:
海外基金