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Morphologic/Neurochemical Correlates of Depression in AD

Morphologic/Neurochemical Correlates of Depression in AD
AD 抑郁症的形态/神经化学相关性
批准号:
7535200
负责人:
GEORGE S ZUBENKO
金额:
$63.41万
依托单位国家:
美国
项目类别:
财政年份:
1992
资助国家:
美国
项目状态:
已结题
起止时间:
1992-09-30 至 2010-11-30
关键词:
AffectAgeAllelesAlzheimer&aposs DiseaseApolipoprotein EApoptosisApoptoticAreaAutopsyBasal Nucleus of MeynertBehaviorBehavioralBiologicalBiological PreservationBiologyBrainBrain StemBrain regionCell DeathCell NucleusCellsCessation of lifeCholine O-AcetyltransferaseChromatinClinicalClinical assessmentsCollaborationsComplicationDNADNA FragmentationDNA Repair EnzymesDataDelusionsDementiaDevelopmentDiagnosisDiagnosticDopamineDorsalElderlyElementsEventFamilyFamily history ofFirst Degree RelativeFreezingFrequenciesFundingGenotypeGeriatric PsychiatryGoalsHallucinationsHigh Pressure Liquid ChromatographyHigh PrevalenceHippocampus (Brain)HourIncidenceInstitutionalizationIntentionInterviewLeadLeftLewy BodiesLongitudinal StudiesMajor Depressive DisorderMeasuresMethodsMood DisordersNational Institute of Mental HealthNatureNeocortexNerve DegenerationNeuronsNeurotransmittersNorepinephrineNuclearOutpatientsPathogenesisPathway interactionsPatientsPerceptionPhysical condensationPredispositionPrevalenceProcessProgress ReportsProteinsPsychotic DisordersQualifyingRecording of previous eventsRecruitment ActivityRecurrenceRelative (related person)ReportingResearchResearch PersonnelResearch Project GrantsRoleSamplingSenile PlaquesSerotoninSeveritiesSiteSpecificityStochastic ProcessesStructureSubstantia nigra structureSymptomsSyndromeTimeTissue SampleTissuesUnited StatesUp-RegulationVariantcaregivingcase controlcholinergicclinical materialdensitydepressiondepressive symptomsdisabilitydisorder controldisturbance in affecteffective therapyexperiencegeriatric depressioninsightknowledge baseneurochemistryneuron lossnormal agingpreventprogramssingle episode major depressive disorder

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DESCRIPTION (provided by applicant): Major Depressive Disorder (MDD) is a common and important complication of Alzheimer's disease (AD) that increases the suffering of patients and their families, produces excess disability, promotes institutionalization, and hastens death. Emerging clinicopathological studies of MDD in AD suggest that the development of this behavioral complication of AD is associated with degeneration of the brainstem aminergic nuclei (SN, DR, LC) and the relative preservation of the cholinergic bnM. These neuropathologic and related neurochemical correlates of AD+MDD appear to be relatively specific for this behavioral complication of AD, and may explain aspects of the course and treatment responsiveness of MDD in this context. We propose to evaluate this primary etiologic hypothesis using 125 histopathologically-confirmed AID cases and controls who were prospectively characterized by a consortium of four NIA-funded ADRCs and the Geriatric Psychiatry Branch, DIRP, NIMI-t. All participating sites employ the Clinical Assessment of Depression in Dementia (CADD), a structured, anchored diagnostic interview that was developed to reliably diagnose and characterize Major Depressive Episodes (MDEs) in this ongoing longitudinal study. Multidimensional assessments of neurodegeneration of the brainstem nuclei are performed using rigorous stereologic analyses of immunostained frozen serial sections, and determinatons of NTs/metabolites in defined cortical and subcortical projection areas are performed using flash-frozen tissue samples by established HPLC methods. Secondary. Hypotheses explore: a) the associations of clinical subtypes on these neuropathologic and neurochemical variables, b) the mechanism of cell death in these regions, and c) the influence of a family history of MDD and APOE genotype on the emergence of MDD in AD. The long-term goal of the proposed research plan is to better define the biological substrates MDD in AD, with the intention of augmenting the knowledge base that will facilitate the development of more effective treatments, and to provide additional insight into the clinical biology of Major Mood Disorders affecting the elderly.
期刊论文(5)
专著(0)
科研奖励(0)
会议论文
No evidence of non-homologous insertions in mouse model of MDD created by replacement of homologous mouse DNA sequence with pathogenic 6-base human CREB1 promoter sequence.
没有证据表明 MDD 小鼠模型中存在非同源插入,该模型是通过用致病性 6 碱基人 CREB1 启动子序列替换同源小鼠 DNA 序列而创建的。
DOI: 10.1002/ajmg.b.32006
发表时间: 2012
期刊: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
影响因子: --
作者: [Zubenko,GeorgeS, Hughes3rd,HughB]
通讯作者: Hughes3rd,HughB
DOI: 10.1002/ajmg.b.31197
发表时间: 2011-07
期刊: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
影响因子: 2.8
作者: [Zubenko, George S., Hughes, Hugh B., III]
通讯作者: Hughes, Hugh B., III
DOI: 10.1002/ajmg.b.32257
发表时间: 2014-09
期刊: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS
影响因子: 2.8
作者: [Zubenko, George S., Hughes, Hugh B., Jordan, Rick M., Lyons-Weiler, James, Cohen, Bruce M.]
通讯作者: Cohen, Bruce M.
GENETICS OF RECURRENT EARLY ONSET DEPRESSION (GENRED)
GENETICS OF RECURRENT EARLY-ONSET DEPRESSION (GENRED)
GENETICS OF RECURRENT EARLY-ONSET DEPRESSION (GENRED)
BIOLOGICAL MARKERS FOR PRIMARY DEMENTIA IN ELDERLY
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