Functional anomaly mapping of aphasia recovery
Functional anomaly mapping of aphasia recovery
批准号:
10398979
负责人:
Andrew T DeMarco
金额:
$12.04万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-07-01 至 2023-06-30
关键词:
AffectAlgorithmsAnatomyAphasiaArchitectureAreaAwardBehavioralBiologicalBlood VesselsBrainCharacteristicsChronicClinicalCommunicationDataData SetDeafferentation procedureDiagnosisDistantExhibitsFunctional Magnetic Resonance ImagingFunctional disorderGoalsIndividualKnowledgeLanguageLeadLeftLengthLesionLocationLongitudinal StudiesLongitudinal prospective studyMachine LearningMapsMeasuresMentorsModelingNational Institute on Deafness and Other Communication DisordersNeuronal PlasticityOutcomePatternPerformancePersonsPhasePhysiologyRecoveryReproducibilityResearchResearch TrainingResidual stateResolutionRestSample SizeScanningSeveritiesSignal TransductionSourceSpecific qualifier valueStrategic PlanningStrokeStructureSymptomsTestingTimeTrainingaphasia recoverybasebehavior measurementbehavioral outcomebiomarker developmentbrain behaviorchronic strokeclinical decision-makingcohortexperienceimaging modalityimprovedmachine learning algorithmmultimodalityneural correlateneurobiological mechanismneuroimagingneurological rehabilitationneuromechanismpost strokeprogramspublic health relevancespatiotemporalstroke recoverystroke survivorstroke-induced aphasiatoolwhite matter
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Project Summary
Difficulty communicating (aphasia) is one of the most common and debilitating results of left-hemisphere
stroke. Although aphasia symptoms are highly variable and recovery is difficult to predict, much research has
shown that lesion size and location are major drivers of aphasia symptoms and recovery. However, this
previous research has only considered direct anatomical damage caused by the lesion. This is a critical
limitation because stroke lesions also cause indirect effects on the function of brain structures distant from the
lesion. Throughout this application, I refer to this as “remote dysfunction.” Although initially thought to resolve
quickly after the stroke, remote dysfunction is now known to persist throughout recovery and independently
contribute to outcomes. Studies of aphasia recovery have focused almost exclusively on the idea of recovery
through reorganization, whereby behavioral improvement occurs through plastic reorganization of brain
networks. These studies have eschewed the older idea that recovery occurs through partial resolution of
remote dysfunction (RRD) caused by lesions. Consequently, it is not clear how RRD contributes to aphasia
recovery. The applicant has developed a new machine learning approach called functional anomaly mapping
(FAM) that uses resting BOLD functional MRI signal to map remote dysfunction throughout the brain in
individual stroke survivors. FAM maps have much better test-retest reliability than current measures, like task-
related fMRI activity and resting state functional connectivity, as well as several other features that make it
promising as a clinically useful tool. The applicant has already demonstrated that remote dysfunction
measured with FAM relates to behavioral outcomes in people with chronic aphasia. During the mentored
phase of this award, the applicant will optimize the FAM approach and test competing hypotheses about the
biological mechanisms generating the remote dysfunction measured in chronic aphasia. During the
independent phase, the applicant proposes a longitudinal study to understand the contribution of RRD to
aphasia recovery. The applicant proposes a comprehensive training plan to expand his knowledge in the
following areas: the biological mechanisms of stroke recovery and neuroplasticity beyond aphasia, machine
learning, biomarker development, and advanced neuroimaging analysis. The research and training during this
award will enable the applicant to develop a long-term, independent research program focused on
understanding the neural correlates of aphasia and developing translational brain measures to inform clinical
decision-making in aphasia neurorehabilitation.
期刊论文(3)
专著(0)
科研奖励(0)
会议论文
Aphasia severity is modulated by race and lesion size in chronic survivors: A retrospective study.
慢性幸存者失语症的严重程度受种族和病变大小的调节:一项回顾性研究。
DOI:
10.1016/j.jcomdis.2022.106270
发表时间:
2022
期刊:
Journal of communication disorders
影响因子:
1.7
作者:
[Gadson,DavetrinaS, Wesley,DeliyaB, vanderStelt,CandaceM, Lacey,Elizabeth, DeMarco,AndrewT, Snider,SarahF, Turkeltaub,PeterE]
通讯作者:
Turkeltaub,PeterE
DOI:
10.1016/j.nicl.2021.102934
发表时间:
2022
期刊:
NeuroImage. Clinical
影响因子:
--
作者:
[McCall JD, Vivian Dickens J, Mandal AS, DeMarco AT, Fama ME, Lacey EH, Kelkar A, Medaglia JD, Turkeltaub PE]
通讯作者:
Turkeltaub PE
Functional anomaly mapping of aphasia recovery
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批准号:10837812
-
项目类别:
-
资助金额:$24.9万
-
财政年份:2023
-
负责人:Andrew T DeMarco
-
依托单位:
Functional anomaly mapping of aphasia recovery
-
批准号:10214766
-
项目类别:
-
资助金额:$12.15万
-
财政年份:2021
-
负责人:Andrew T DeMarco
-
依托单位:
Neural correlates of treatment-induced recovery of phonological processing in chronic aphasia
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批准号:8990733
-
项目类别:
-
资助金额:$3.91万
-
财政年份:2015
-
负责人:Andrew T DeMarco
-
依托单位:
Neural correlates of treatment-induced recovery of phonological processing in chronic aphasia
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批准号:8907444
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项目类别:
-
资助金额:$3.86万
-
财政年份:2015
-
负责人:Andrew T DeMarco
-
依托单位:
海外基金