Inflammatory Networks Mediating Cognitive Decline In Preclinical Alzheimers Disease
Inflammatory Networks Mediating Cognitive Decline In Preclinical Alzheimers Disease
批准号:
10162456
负责人:
JAGAN AYYAPPAN PILLAI
金额:
$17.39万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-05-01 至 2024-04-30
关键词:
AcuteAddressAgeAlzheimer&aposs DiseaseAlzheimer&aposs disease modelAlzheimer&aposs disease patientAlzheimer&aposs disease riskAmyloidAmyloid beta-42Amyloid beta-ProteinAnatomyAnimal ModelAwardBehavioralBioinformaticsBiological MarkersBlood - brain barrier anatomyBrainCCL2 geneCause of DeathCerebrospinal FluidClinicClinicalClinical ResearchClinical TrialsCognitionCognition DisordersCognitiveDataDatabasesDementiaDiseaseDisease ProgressionEarly InterventionElderlyFactor AnalysisFoundationsFundingFutureGelatinase AGene ExpressionGene Expression ProfileGenesGenetic PolymorphismGenetic RiskGenotypeGoalsGrantImmunobiologyImpaired cognitionIndividualInflammatoryInflammatory ResponseInterventionK-Series Research Career ProgramsKnowledgeLaboratory ResearchMMP2 geneMacrophage Inflammatory Protein-1Magnetic Resonance ImagingMediatingMedicineModelingMolecularNerve DegenerationNervous System PhysiologyNeurodegenerative DisordersNeurologistNeuron-Specific EnolaseNeurosciences ResearchOutcomePatientsPeripheral Blood Mononuclear CellPlasmaPopulationPredictive FactorProteinsPublic HealthReceptors, Tumor Necrosis Factor, Type IIResearchResearch PersonnelRiskRoleSamplingSerumStructureSymptomsTIMP1 geneTNFRSF1B geneTREM2 geneTechniquesTherapeuticTherapeutic InterventionTimeTrainingUrsidae FamilyWorkWritingage groupapolipoprotein E-4bioinformatics toolchemokineclinical outcome measurescognitive changecognitive neurosciencecognitive testingcytokinedesignexperiencegenome wide association studygenome-wideimmunomodulatory therapiesinflammatory markerinsightmild cognitive impairmentmultidisciplinaryneuroimagingneuroinflammationneuropathologynovel therapeutic interventionpre-clinicalprecision medicinepreservationpreventrisk variantskillssystemic inflammatory responsetargeted treatmenttau Proteinstranscriptome sequencingtranslational study
中文摘要
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英文摘要
PROJECT SUMMARY/ABSTRACT
Alzheimer's disease (AD) is a devastating neurodegenerative disease that causes progressive
cognitive decline towards dementia. One in nine people over 65 yrs of age in the US has AD and it is the fifth-
leading cause of death in this age group. The over 65 population is expected to double by 2050. Delineating
factors that predict and prevent cognitive decline related to AD are hugely important but are still poorly
understood.
This Career Development Award will provide additional training and research opportunities in
bioinformatics and neuroinflammation for Dr. Pillai to advance his clinical research skills to address a current
knowledge gap in the role for inflammatory factors in AD progression. He is a behavioral neurologist
experienced in cognitive neuroscience research with a long-term goal to establish a programmatic body of
research using bioinformatics tools to delineate the molecular factors that underpin cognitive decline and
disease progression among neurodegenerative diseases.
Knowledge of inflammatory factors that drive AD progression will be critical in designing novel
therapeutic strategies to prevent cognitive decline. This award will aid him in achieving these goals through a
structured training plan that includes formal course work in bioinformatics and statistical techniques, as well as
relevant laboratory and clinical research in the immunobiology of AD. He will also receive additional training in
grant writing and the design and administration of clinical trials research to facilitate his future focus on bringing
bioinformatics insights from large data to bear fruitful impact in the clinic.
The research at the foundation of the current application is a clinical translational study that aims to
characterize the temporal course of neuroinflammation, blood brain barrier (BBB) integrity and
neurodegeneration in AD. Dr.Pillai's preliminary studies in this direction, funded by the Alzheimer Association,
suggest that there is a strong relationship between the above three domains, among AD patients at the stage
of mild cognitive impairment (MCI). The current award will help Dr.Pillai confirm and extend these insights
among healthy, cognitively intact elders who are APOE ε4 risk gene carriers, a significant percentage of whom
may be in the preclinical stage of AD. We hypothesize that higher levels of specific baseline cerebrospinal fluid
inflammatory markers and BBB break down markers correlate with higher levels of neurodegeneration and
impacts cognitive decline over 24 months among these subjects. We will confirm and validate the temporal
course of inflammatory protein changes with longitudinal multiplex biomarker and genome wide expression
changes over 24 months and against data from other large national data (Alzheimer's Disease Neuroimaging
Initiative, Accelerating Medicines Partnership-AD). This research will characterize individual propensities for
deleterious inflammatory responses that would be useful for future precision medicine interventions against
neuroinflammation in AD to prevent disease progression and cognitive decline
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DOI:
10.1038/s41598-020-77503-2
发表时间:
2020-11-26
期刊:
Scientific reports
影响因子:
4.6
作者:
[Pillai JA, Larvie M, Chen J, Crawford A, Cummings JL, Jones SE]
通讯作者:
Jones SE
DOI:
10.1186/s13195-023-01203-y
发表时间:
2023-03-16
期刊:
Alzheimer's research & therapy
影响因子:
--
作者:
[]
通讯作者:
Highly Elevated Cerebrospinal Fluid Total Tau Level Reflects Higher Likelihood of Non-Amnestic Subtype of Alzheimer's Disease.
脑脊液总 Tau 水平升高表明阿尔茨海默病非遗忘亚型的可能性较高。
DOI:
10.3233/jad-190519
发表时间:
2019
期刊:
Journal of Alzheimer's disease : JAD
影响因子:
--
作者:
[Pillai,JaganA, Bonner-Jackson,Aaron, Bekris,LynnM, Safar,Jiri, Bena,Jim, Leverenz,JamesB]
通讯作者:
Leverenz,JamesB
DOI:
10.1186/s13195-021-00771-1
发表时间:
2021-01-23
期刊:
Alzheimer's research & therapy
影响因子:
--
作者:
[Pillai JA, Bena J, Bonner-Jackson A, Leverenz JB]
通讯作者:
Leverenz JB
DOI:
10.3389/fnagi.2021.638922
发表时间:
2021
期刊:
Frontiers in aging neuroscience
影响因子:
4.8
作者:
[Pillai JA, Bebek G, Khrestian M, Bena J, Bergmann CC, Bush WS, Leverenz JB, Bekris LM]
通讯作者:
Bekris LM
共 7 条
Immune cell activation and associated blood brain barrier changes across different stages of Alzheimer's disease
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批准号:10515907
-
项目类别:
-
资助金额:$77.93万
-
财政年份:2022
-
负责人:JAGAN AYYAPPAN PILLAI
-
依托单位:
Immune cell activation and associated blood brain barrier changes across different stages of Alzheimer's disease
-
批准号:10688122
-
项目类别:
-
资助金额:$75.33万
-
财政年份:2022
-
负责人:JAGAN AYYAPPAN PILLAI
-
依托单位:
Pyroglutamate-modified Amyloid-B protein as a marker for future cognitive decline in preclinical Alzheimers disease
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批准号:9912697
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项目类别:
-
资助金额:$16.08万
-
财政年份:2019
-
负责人:JAGAN AYYAPPAN PILLAI
-
依托单位:
Inflammatory Networks Mediating Cognitive Decline In Preclinical Alzheimers Disease
-
批准号:9916678
-
项目类别:
-
资助金额:$18.29万
-
财政年份:2017
-
负责人:JAGAN AYYAPPAN PILLAI
-
依托单位:
Inflammatory Networks Mediating Cognitive Decline In Preclinical Alzheimers Disease
-
批准号:9295636
-
项目类别:
-
资助金额:$18.71万
-
财政年份:2017
-
负责人:JAGAN AYYAPPAN PILLAI
-
依托单位:
Inflammatory Networks Mediating Cognitive Decline In Preclinical Alzheimers Disease
-
批准号:9477445
-
项目类别:
-
资助金额:$18.76万
-
财政年份:2017
-
负责人:JAGAN AYYAPPAN PILLAI
-
依托单位:
海外基金