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:
9764219
负责人:
Sandra A Billinger
金额:
$240.92万
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:
已结题
起止时间:
2018-09-01 至 2023-05-31
关键词:
AdvocateAgeAlzheimer&aposs DiseaseAlzheimer’s disease biomarkerAmyloidApolipoprotein EAtrophicBiological MarkersBlood Flow VelocityBlood PressureBrainCarbon DioxideCerebral small vessel diseaseCerebrovascular CirculationCerebrumClassificationCohort StudiesDataDatabasesDeteriorationDiagnosisDisease ProgressionEducationElderlyEvaluationGenderGenotypeGoalsImpaired cognitionMagnetic Resonance ImagingMeasuresMethodologyModelingMonitorNear-Infrared SpectroscopyNeurocognitiveNeuropsychological TestsOutputPathologicPatientsPerfusionPersonsPlasmaPositron-Emission TomographyPublishingRegulationRetrospective StudiesSiteStructureVasomotorWhite Matter Hyperintensityamnestic mild cognitive impairmentbasecerebral hemodynamicscerebrovascularcohortfollow-uphemodynamicsimprovedmild cognitive impairmentnovelportabilitypredictive modelingprimary care settingresponsescreeningtissue oxygenationwhite matter
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(0)
专著(0)
科研奖励(0)
会议论文
Model-based cerebrovascular markers extracted from hemodynamic data for diagnosing MCI or AD and predicting disease progression.
-
批准号:10187475
-
项目类别:
-
资助金额:$229.96万
-
财政年份:2018
-
负责人:Sandra A Billinger
-
依托单位:
Revision Supplement: Model-based cerebrovascular markers extracted from hemodynamic data for diagnosing MCI or AD and predicting disease progression
-
批准号:10242469
-
项目类别:
-
资助金额:$50.14万
-
财政年份:2018
-
负责人:Sandra A Billinger
-
依托单位:
Model-based cerebrovascular markers extracted from hemodynamic data for diagnosing MCI or AD and predicting disease progression.
-
批准号:10404604
-
项目类别:
-
资助金额:$179.36万
-
财政年份:2018
-
负责人:Sandra A Billinger
-
依托单位:
Examining Vascular Regulation Following Acute Stroke
-
批准号:8460137
-
项目类别:
-
资助金额:$10.09万
-
财政年份:2011
-
负责人:Sandra A Billinger
-
依托单位:
Examining Vascular Regulation Following Acute Stroke
-
批准号:8676494
-
项目类别:
-
资助金额:$10.15万
-
财政年份:2011
-
负责人:Sandra A Billinger
-
依托单位:
Examining Vascular Regulation Following Acute Stroke
-
批准号:8188791
-
项目类别:
-
资助金额:$10.01万
-
财政年份:2011
-
负责人:Sandra A Billinger
-
依托单位:
Examining Vascular Regulation Following Acute Stroke
-
批准号:8848408
-
项目类别:
-
资助金额:$10.22万
-
财政年份:2011
-
负责人:Sandra A Billinger
-
依托单位:
Examining Vascular Regulation Following Acute Stroke
-
批准号:8310933
-
项目类别:
-
资助金额:$10.01万
-
财政年份:2011
-
负责人:Sandra A Billinger
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
-
批准号:JCZRQN202500010
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
-
批准号:2025JJ70209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
-
批准号:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
-
批准号:2023JJ50274
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
-
批准号:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
-
批准号:81973577
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
-
批准号:81602908
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: