Pattern Analysis of fMRI via machine learning/sparse models: application to brain development
Pattern Analysis of fMRI via machine learning/sparse models: application to brain development
批准号:
9155330
负责人:
Christos Davatzikos
金额:
$49.1万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-07-01 至 2020-03-31
关键词:
AddressAdolescentAgeAlgorithmsAnatomyBiologicalBiological MarkersBrainBrain regionClassificationClinical DataCommunitiesDataDevelopmentDiagnosisDictionaryFunctional ImagingFunctional Magnetic Resonance ImagingGoalsHeterogeneityImageIndividualLinkMachine LearningMeasurementMeasuresMethodologyMethodsModelingNeurosciencesOutcomePathologicPathway AnalysisPatternPattern RecognitionPhiladelphiaPopulationPsychotic DisordersResourcesRestRiskSamplingShapesSubgroupSymptomsTechniquesTestingWorkYouthabstractingbasebrain abnormalitiesclinical biomarkerscognitive functioncohortconnectomefollow-uphuman dataimprovedindexinginterestlearning strategyneuroimagingneuropsychiatric disordernovelsignal processingtooltrend
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Abstract
Resting state fMRI (rsfMRI) provides reproducible, task-independent biomarkers of coherent
functional activity linking different brain regions. The main goal of the proposed project is to leverage
advances in signal processing and machine learning methods to derive clinically useful biomarkers
based on patterns of functional connectivity, and to test these biomarkers in a large study of brain
development. Central to our methodology are 1) computing a subject-specific functional parcellation
of the brain, which defines nodes for characterizing individualized functional brain networks; 2)
extracting sparse connectivity patterns for robustly representing brain networks; 3) capturing
heterogeneity in brain networks across individuals in a given population; and 4) deriving individualized
predictive indices of psychosis risk from brain connectivity in a large study of brain development. This
novel suite of functional connectivity analysis tools will be developed and validated based on data
from the Human Connectome Project and the Philadelphia Neurodevelopmental Cohort (PNC).
Finally, these techniques will be applied to PNC data in order to delineate heterogeneity in network
development in youth with psychosis-spectrum symptoms. Our hypothesis is that patterns of
functional connectivity in adolescents with psychosis-spectrum symptoms will be different from those
in typically developing adolescents, and this difference will display a high degree of heterogeneity that
is linked to underlying heterogeneity in pathologic neurodevelopmental trajectories. Moreover, we
expect that machine learning techniques will allow us to predict on an individual basis which
adolescents with psychosis-spectrum symptoms will remain stable, which will revert to normal, and
which will progress to psychosis, based on their baseline functional connectivity signatures. Our
methods are generally applicable to rsfMRI studies for detecting and quantifying spatio-temporal
functional connectivity patterns in diverse fields, including diagnosing brain abnormalities in
neuropsychiatric diseases, and finding associations of functional connectivity with different cognitive
functions. All methods will be made publicly available and form an important new resource for the
broader neuroscience community.
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