Model-based cerebrovascular markers extracted from hemodynamic data for diagnosing MCI or AD and predicting disease progression.
Model-based cerebrovascular markers extracted from hemodynamic data for diagnosing MCI or AD and predicting disease progression.
批准号:
10404604
负责人:
Sandra A Billinger
金额:
$179.36万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
未结题
起止时间:
2018-09-01 至 2025-05-31
关键词:
AdvocateAgeAlzheimer&aposs DiseaseAlzheimer&aposs disease patientAlzheimer’s disease biomarkerApolipoprotein EAtrophicBiological MarkersBlood Flow VelocityBlood PressureBrainCarbon DioxideCerebral small vessel diseaseCerebrovascular CirculationCerebrumClassificationCohort StudiesDataDatabasesDeteriorationDiagnosisDisease ProgressionEducationElderlyEvaluationGenderGenotypeGoalsImpaired cognitionMagnetic Resonance ImagingMeasuresMethodologyModelingMonitorNear-Infrared SpectroscopyNeurocognitiveNeuropsychological TestsOutputPathologicPatientsPerfusionPersonsPlasmaPositron-Emission TomographyPublishingRegulationRetrospective StudiesSiteVasomotorWhite Matter Hyperintensityamnestic mild cognitive impairmentbasecerebral hemodynamicscerebrovascularcohortfollow-uphemodynamicsimprovedmild cognitive impairmentnovelportabilitypredictive modelingprimary care settingresponsescreeningtissue oxygenationwhite matterβ-amyloid burden
中文摘要
点击翻译按钮获取中文摘要
英文摘要
"Model-based cerebrovascular markers extracted from hemodynamic data for
non-invasive, portable and inexpensive diagnosis of MCI or mild AD and prediction of
disease progression"
PROJECT SUMMARY
The goal of the proposed multi-PI project is to establish proof of concept for the utility of a new
class of cerebrovascular markers that may aid in the improved diagnosis and prediction of
disease progression in Mild Cognitive Impairment (MCI) and mild Alzheimer's disease (AD).
The means for obtaining these markers are non-invasive, inexpensive and portable, so that they
can be used for screening in a primary-care setting. The scientific rationale for this new class of
cerebrovascular markers is provided by the recent promising results of our group and the
mounting evidence of a strong correlation between MCI/AD and cerebrovascular dysregulation.
A recently published retrospective study on a large cohort of 1,171 subjects from the ADNI
database utilized multi-factorial data-driven analysis to assess the relation between MCI/AD
disease progression and commonly used biomarkers (obtained from MRI/PET and plasma/CSF)
and concluded that cerebrovascular dysregulation is the earliest and strongest pathologic
factor associated with AD progression, corroborating the hypothesis of cerebrovascular
dysregulation.
Quantification of cerebrovascular dysregulation in that large-cohort study was achieved through
analysis of ASL-MRI data of cerebral perfusion. We propose instead to explore a novel
integrative dynamic modeling approach that analyzes the cerebral hemodynamics of
persons with no cognitive impairment and MCI/AD patients with a methodology that yields input-
output predictive models of the dynamic relationships between changes in beat-to-beat cerebral
blood flow velocity (via Transcranial Doppler) or cerebral tissue oxygenation (via Near Infrared
Spectroscopy) in response to changes in arterial blood pressure and end-tidal CO2 data. The
obtained data-based models are subsequently used to compute markers of the dynamics of
cerebrovascular regulation. Initial results of the advocated approach have achieved
statistically significant delineation between 46 MCI patients and 20 age-matched controls on the
basis of a model-based marker of dynamic vasomotor reactivity (DVR). Evaluation of the
DVR marker against established MRI-based and PET-based biomarkers, as well as
neuropsychological test data, from the larger cohort of the proposed project offers the promise
of portable, non-invasive, inexpensive and sensitive means for detecting cerebrovascular
dysregulation at the early stages of MCI or mild AD, and monitoring disease progression.
Important co-variates of this study include age, gender, education, ApoE genotype, site and
amyloid burden.
期刊论文(9)
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Clinical relevance of brachial pulse pressure as a measure of cerebrovascular disease risk.
肱动脉脉压作为脑血管疾病风险衡量指标的临床相关性。
DOI:
10.1111/jch.13582
发表时间:
2019
期刊:
Journal of clinical hypertension (Greenwich, Conn.)
影响因子:
--
作者:
[Perdomo,SophyJ]
通讯作者:
Perdomo,SophyJ
Closed-Loop Dynamic Modeling of the Heart-Rate Reflex to Concurrent Spontaneous Changes of Arterial Blood Pressure and CO2 Tension: Quantification of the Effects of Mild Cognitive Impairment.
心率反射对动脉血压和二氧化碳张力同时自发变化的闭环动态建模:轻度认知障碍影响的量化。
DOI:
10.1109/tbme.2021.3070900
发表时间:
2021
期刊:
IEEE transactions on bio-medical engineering
影响因子:
--
作者:
[Marmarelis,Vasilis, Shin,Dae, Zhang,Rong]
通讯作者:
Zhang,Rong
DOI:
10.1109/ojemb.2020.3008313
发表时间:
2020
期刊:
IEEE open journal of engineering in medicine and biology
影响因子:
5.8
作者:
[Marmarelis VZ]
通讯作者:
Marmarelis VZ
DOI:
10.1016/j.jstrokecerebrovasdis.2023.107454
发表时间:
2023-11-04
期刊:
JOURNAL OF STROKE & CEREBROVASCULAR DISEASES
影响因子:
2.5
作者:
[Lakatos,Lehel Barna, Shin,Dae C., Bolognese,Manuel]
通讯作者:
Bolognese,Manuel
Model-based cerebrovascular markers extracted from hemodynamic data for diagnosing MCI or AD and predicting disease progression.
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Revision Supplement: Model-based cerebrovascular markers extracted from hemodynamic data for diagnosing MCI or AD and predicting disease progression
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Examining Vascular Regulation Following Acute Stroke
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资助金额:$10.01万
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财政年份:2011
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