Cortical functional connectivity as an early biomarker of recovery in spinal cord injury
Cortical functional connectivity as an early biomarker of recovery in spinal cord injury
批准号:
10174454
负责人:
ANN S CHOE
金额:
$8.08万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-06-01 至 2021-08-31
关键词:
Biological MarkersBrainChronicClassificationClinicalCluster AnalysisDataEarly DiagnosisElectric StimulationElectric Stimulation TherapyFinancial HardshipFunctional Magnetic Resonance ImagingGoalsInternationalInterventionKnowledgeMeasuresMethodsModificationMonitorMotorMovementNervous System TraumaNeurologicNeurological outcomeOutcome MeasurePatientsPerformanceRecoveryRestSpinal cord injurySpinal cord injury patientsSystemTestingTherapeutic InterventionTimeearly detection biomarkersfunctional electrical stimulationfunctional lossimaging biomarkerindependent component analysisintervention programnon-invasive imagingpatient populationpreservationpreventprogramsresponsetool
中文摘要
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英文摘要
PROJECT SUMMARY
Early detection of response to spinal cord injury (SCI) therapeutic intervention programs is vital, as it will
enable early termination of intervention in non-responding patients, prevent unnecessary financial burden, and
allow for timely program modifications. In this project, we propose that resting state functional MRI (rsfMRI) can
be used to detect early brain functional network changes that occur during an intervention, and that the
changes will be predictive of recovery in chronic SCI patients. The long-term goal of this study is to establish
rsfMRI as a new imaging biomarker that is predictive of progress towards recovery in response to therapy.
International Standard of Neurological Classification for Spinal Cord Injury (ISNCSCI) scoring system is the
most widely used clinical classification system of SCI that describes neurological injury level and degree of
functional preservation. It is also used to monitor the progress and response to interventions such as functional
electrical stimulation (FES) therapy. However, monitoring responses using ISNSCI is challenging because its
ability to describe the degree of functional loss is limited. Therefore, there is a need in the field of SCI for a
biomarker that is more sensitive to changes in function.
In Aim 1 of this project, we will characterize the baseline time profile of the cortical reorganization in chronic
SCI patients that occurs during a 4-weeks program of passive FES cycling, where movement is driven only by
the cycle’s motor (no electric stimulation). RsfMRI data of the patients acquired at weeks 0, 2, and 4 will be
analyzed to perform functional parcellation of the sensorimotor cortex, using the independent component
analysis (ICA) and spectral clustering analysis (SCA) methods. BNC measures of the resulting sensorimotor
cortex parcels will then be calculated. ISNCSCI scores of the patients will also be measured at weeks 0, 2, and
4, to test the hypothesis that we will observe minimal to no changes in sensorimotor cortex BNC and ISNCSCI
scores of the patients after 4 weeks of passive FES cycling. In Aim 2 of this project, we will characterize the
time profile of the cortical reorganization in chronic SCI patients that occurs during the four-week (active) FES
cycling. Specifically, we predict that we will observe early functional network changes in the sensorimotor
cortex of SCI patients (measured using BNC) at week 2 of the four-week FES cycling program, which will be
predictive of changes in ISNSCI scores (neurological outcomes) at week 4.
If successful, the study will: 1) provide a new and effective clinical tool to study plastic cortical changes that
occur after SCI, 2) provide a new non-invasive imaging biomarker that is predictive of progress towards
recovery in response to therapy, and 3) extend our knowledge about the functional reorganization that takes
place during and after therapeutic intervention.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
DOI:
10.1371/journal.pone.0244756
发表时间:
2021
期刊:
PloS one
影响因子:
3.7
作者:
[Choe AS, Tang B, Smith KR, Honari H, Lindquist MA, Caffo BS, Pekar JJ]
通讯作者:
Pekar JJ
国内基金
海外基金
Sitagliptin通过microbiota-gut-brain轴在2型糖尿病致阿尔茨海默样变中的脑保护作用机制
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批准号:81801389
-
项目类别:青年科学基金项目
-
资助金额:21.0万元
-
批准年份:2018
-
负责人:田茗源
-
依托单位:
平扫描数据导引的超低剂量Brain-PCT成像新方法研究
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批准号:81101046
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项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2011
-
负责人:黄静
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依托单位: