Neurocognitive Mechanisms of Positive Intervention Response in Reading Disability
Neurocognitive Mechanisms of Positive Intervention Response in Reading Disability
批准号:
10747218
负责人:
Steven Lee Meisler
金额:
$2.66万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
已结题
起止时间:
2023-09-30 至 2024-05-30
关键词:
AchievementAdolescenceAdultAffectAgeBehavioralBrainChildClassificationCognitionCognitiveComplementControl GroupsDevelopmentDiffusion Magnetic Resonance ImagingDyslexiaEducational InterventionExhibitsFellowshipFunctional Magnetic Resonance ImagingFutureGoalsImpairmentInferior frontal gyrusInstructionIntelligenceInterventionIntervention StudiesKnowledgeLanguageLearningLearning DisabilitiesLeftLinguisticsMeasuresMethodsNeuroanatomyNeurocognitiveOutcomeParticipantProcessPropertyReaderReadingReading DisabilitiesReportingResearchResearch DesignResearch PersonnelRestRoleScanningSchoolsScienceShort-Term MemorySocioeconomic StatusSpecificityStandardizationTestingTimeTrainingTranslational ResearchVariantWorkbasecareercognitive neurosciencecognitive processdesigneighth gradeexecutive functionfunctional MRI scanimaging studyimprovedinsightlexicalmultimodal neuroimagingneuralneuroimagingnovelphonological awarenessphonologyrecruitremediationresponsesexskillsverbalvirtualwhite matter
中文摘要
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英文摘要
PROJECT SUMMARY / ABSTRACT
Reading disabilities (RD) are the most common learning disability and are characterized by deficits in word
reading accuracy and/or fluency that are not explained by general intelligence levels. Without targeted
educational intervention, these deficits may persist through adolescence into adulthood. While interventions have
been shown to, on average, improve reading outcomes among children with RD, gains in skill are heterogeneous.
Functional MRI (fMRI) studies have revealed, unexpectedly, that children with RD who substantially improve
in reading appear to do so by engaging the right inferior frontal gyrus (rIFG), despite typical reading usually
involving a left-lateralized language network. Several cognitive processes tend to recruit the rIFG, ranging from
verbal processes to domain-general skills such as working memory. All of these skills may support achievement
in reading. However, no study has rigorously investigated what process is signified by rIFG among responders
to intervention. In addition, few studies have examined how structural properties of white matter emanating from
the rIFG relate to intervention responses. In this project, I will use multimodal neuroimaging to, for the first
time, characterize the role of the rIFG in reading improvement among children with RD. I will recruit and
characterize 90 7th-8th grade children across three groups that will be studied in subsequent aims. I will classify
children with RD into two groups based on whether their age-standardized reading skills improved relative to
age-expected gains (RD+) or not (RD-) following reading instruction. The third group will include typical readers
(TR) matched in age, sex, and socioeconomic status. Aim 1 is to replicate findings of more rIFG activity
while reading among RD+ compared to RD- and TR. For this aim, participants will undergo fMRI scanning
while completing a word reading task. We will also investigate cognitive differences between RD+, RD-, and TR.
Aim 2 will be to investigate what processes are signified by rIFG activation. We will collect fMRI in
participants while they complete language and working memory localizers, and then find the portion of the rIFG
that is most sensitive to each task in each child. We will also collect diffusion-weighted images. We will then
investigate hypotheses that language, but not working memory, regions in RD+ compared to RD- and TR, are:
(1) more active during reading; (2) more functionally connected to the language network during reading; and (3)
more structurally connected to the language network. Findings from these aims will shed further insight into the
neural bases of better or worse response to reading instruction. Our results will carry important implications for
designing remediation strategies for children with RD. The novel and carefully designed methods and analyses
employed in this project will serve to guide future translational neuroimaging research in RD. Through this project,
I will satisfy fellowship training goals by: (1) advancing my knowledge of RD and its treatment; (2) learning about
study design and execution; (3) honing my neuroimaging analysis skills; (4) gaining translational skills in working
with educators and children; and (5) enhancing my professional development towards a career in science.
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