Awareness of Deficits in Dementia
Awareness of Deficits in Dementia
批准号:
8281580
负责人:
HOWARD J ROSEN
金额:
$30.52万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-06-01 至 2015-05-31
关键词:
AccountingAgeAlzheimer&aposs DiseaseAwarenessBehaviorBrain imagingBrain regionCaregiversCerebrumCognitiveConsciousDataDementiaDiagnosticDiseaseEmotionalEmotionsEnsureEpisodic memoryEvaluationEventFailureFamilyFamily CaregiverFeelingFrontotemporal DementiaFunctional disorderGalvanic Skin ResponseGoalsHealthHeart RateHemispatial NeglectHippocampus (Brain)Home environmentIndividualInjuryJudgmentKnowledgeLeadLearningLifeMagnetic Resonance ImagingMeasuresMedialMemoryModelingMonitorMotivationNerve DegenerationNeurologicParahippocampal GyrusParietal LobeParticipantPatientsPerformancePhysiologic MonitoringPhysiologicalPlayProcessQuality of lifeQuestionnairesRecommendationRehabilitation therapyRelative (related person)ResistanceRisk BehaviorsRoleSafetySelf PerceptionSemanticsSocietiesStructureSupervisionSyndromeSystemTestingThinkingTimeTissuesUpdateWorkbasebehavior measurementbehavior testcompliance behaviordisabilityentorhinal cortexexecutive functionexpectationfallsgray matterneglectnervous system disorderneuromechanismpreventpublic health relevanceresponsestandard measure
中文摘要
描述(由申请人提供):这项提案描述了一项研究痴呆症患者对自身残疾缺乏认识的计划,称为病感失认症。病感缺失会导致患者的残疾,并让家人和照顾者感到沮丧。缺乏意识可能会阻止患者遵守治疗建议,并导致他们追求超出他们限制的潜在危险行为,需要监督以确保他们的安全。虽然病感失认症在阿尔茨海默病中非常常见,但在额颞痴呆中更常见,其原因尚不清楚。我们已经开发了一个模型,试图解释病感失认症是如何从特定认知能力的失败中发展起来的,包括监测一个人的表现和情绪,我们还制定了一项计划,以测试这些因素是否导致病感失认症,以及在阿尔茨海默病和额颞痴呆患者中,影响因素是否不同。我们将研究100名健康的老年人,50名阿尔茨海默病患者和50名额颞部痴呆患者。我们将追求以下具体目标:a)确定在AD和FTD中,表现监测、其他额叶/执行功能、记忆和情绪反应对失认症的相对贡献。我们假设:1)在FTD中,即使在考虑了记忆和执行功能的贡献后,认知任务中的操作监控和生理激活也会与病感失认相关。2)在AD中,而不是在FTD中,对最近认知测试表现的记忆将对失认症做出重大贡献。我们假设:1)在控制了其他相关大脑区域的贡献后,右侧内侧眶前皮质的组织丢失将预测测试中的生理激活、对行为监控的行为估计以及FTD和AD的整体自我意识水平。2)在考虑内侧OFC的影响后,内侧颞区(海马区、内嗅皮层、海马旁回)的组织丢失将显著预测AD患者的整体自我意识水平。]为了检验性能监控、生理激活和病感失认症之间的关系:我们假设认知测试中的生理激活将与性能监控的行为测量(错误后减慢[和FOK降低])相关,并与诊断组的整体自我意识水平相关。如果这些假设得到证实,我们将更清楚地了解为什么痴呆症患者没有意识到自己的缺陷。
与公共卫生相关:痴呆症患者通常没有意识到或略微意识到他们的思维问题以及这些缺陷对他们生活的影响。这个项目将试图通过神经科学家开发的认知测试和脑成像来理解为什么痴呆症患者对自己的残疾意识如此薄弱。
英文摘要
DESCRIPTION (provided by applicant): This proposal describes a plan to study lack of awareness of one's disabiltities, called anosognosia, in patients with dementia. Anosognosia contributes to patients' disabilities and frustrates families and caregivers. Lack of awareness may prevent patients from adhering to treatment recommendations, and causes them to pursue potentially risky behaviors that are beyond their limits, requiring supervision to ensure their safety. Although anosognoia is very common in Alzheimer's disease, it is even more common in Frontotemporal dementia, and the reasons for this are not clear. We have developed a model attempting to explain how anosognosia could develop from failures of specific cognitive abilities, including monitoring one's performance and emotion, and we have devised a plan to test whether these factors contribute to anosognosia, and whether the contributing factors differ in patients with Alzheimer's disease and Frontotemporal dementia. We will study 100 healthy older individuals, 50 patients with Alzheimer's disease, and 50 patients with Frontotemporal dementia. We will pursue the following specific aims: A) To define the relative contributions of performance monitoring, other frontal/executive functions, memory, and emotional reactivity to anosognosia in AD and FTD. We hypothesize that: 1) In FTD, performance monitoring and physiological activation during cognitive tasks will be correlated with anosognosia even after accounting for the contributions of memory and executive functions. 2) In AD, but not FTD, memory for recent performance on cognitive testing will make a significant contribution to anosognosia.; We hypothesize that 1) tissue loss in the right medial orbitofrontal cortex will predict physiological activation during testing, behavioral estimates of performance monitoring, and overall level of self-awareness in both FTD and AD [after controlling for the contributions of other relevant brain regions. 2) tissue loss in medial temporal regions (hippocampus, entorhinal cortex, parahippocampal gyrus) will significantly predict overall level of self awareness in AD, after the effects of medial OFC are taken into account.] To examine the relationship between performance monitoring, physiological activation, and anosognosia: We hypothesize that physiological activation during cognitive testing will correlate with behavioral measures of performance-monitoring (post-error slowing [and decreased FOK]) and with overall level of self- awareness across diagnostic groups. If these hypotheses are confirmed, we will have a much clearer idea of why patients with dementia are not aware of their deficits.
PUBLIC HEALTH RELEVANCE: Patients with dementia are usually unaware, or marginally aware of their thinking problems and the effects these deficits have on their life. This project will attempt to understand why patients with dementia have such poor awareness of their disability using cognitive tests developed by neuroscientists, and using brain imaging.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Core F: Neuroimaging Core
-
批准号:10647912
-
项目类别:
-
资助金额:$36.52万
-
财政年份:2019
-
负责人:HOWARD J ROSEN
-
依托单位:
Project 1
-
批准号:10228132
-
项目类别:
-
资助金额:$1.17万
-
财政年份:2019
-
负责人:HOWARD J ROSEN
-
依托单位:
Core F: Neuroimaging Core
-
批准号:10431785
-
项目类别:
-
资助金额:$49.4万
-
财政年份:2019
-
负责人:HOWARD J ROSEN
-
依托单位:
Project 1
-
批准号:10208708
-
项目类别:
-
资助金额:$37.72万
-
财政年份:2019
-
负责人:HOWARD J ROSEN
-
依托单位:
Project 1
-
批准号:9802933
-
项目类别:
-
资助金额:$40.15万
-
财政年份:2019
-
负责人:HOWARD J ROSEN
-
依托单位:
Project 1
-
批准号:10450023
-
项目类别:
-
资助金额:$37.72万
-
财政年份:2019
-
负责人:HOWARD J ROSEN
-
依托单位:
PREDICT-ADFTD: Multimodal Imaging Prediction of AD/FTD and Differential Diagnosis
-
批准号:9240349
-
项目类别:
-
资助金额:$72.32万
-
财政年份:2017
-
负责人:HOWARD J ROSEN
-
依托单位:
PREDICT-FTD: Multimodal Imaging Prediction of FTLD Subtypes.
-
批准号:10915129
-
项目类别:
-
资助金额:$140.83万
-
财政年份:2017
-
负责人:HOWARD J ROSEN
-
依托单位:
PREDICT-ADFTD: Multimodal Imaging Prediction of AD/FTD and Differential Diagnosis
-
批准号:10397226
-
项目类别:
-
资助金额:$53.94万
-
财政年份:2017
-
负责人:HOWARD J ROSEN
-
依托单位:
Multimodal Imaging in Frontotemporal Degeneration
-
批准号:10343692
-
项目类别:
-
资助金额:$19.16万
-
财政年份:2013
-
负责人:HOWARD J ROSEN
-
依托单位:
Multimodal imaging in frontotemporal degeneration
-
批准号:8724327
-
项目类别:
-
资助金额:$18.11万
-
财政年份:2013
-
负责人:HOWARD J ROSEN
-
依托单位:
Multimodal Imaging in Frontotemporal Degeneration
-
批准号:10555216
-
项目类别:
-
资助金额:$19.16万
-
财政年份:2013
-
负责人:HOWARD J ROSEN
-
依托单位:
Establishing Therapeutic Efficacy in Frontotemporal Degeneration
-
批准号:8652131
-
项目类别:
-
资助金额:$5.0万
-
财政年份:2013
-
负责人:HOWARD J ROSEN
-
依托单位:
Multimodal imaging in frontotemporal degeneration
-
批准号:8850370
-
项目类别:
-
资助金额:$18.11万
-
财政年份:2013
-
负责人:HOWARD J ROSEN
-
依托单位:
Multimodal imaging in frontotemporal degeneration
-
批准号:8567416
-
项目类别:
-
资助金额:$18.11万
-
财政年份:2013
-
负责人:HOWARD J ROSEN
-
依托单位:
Multimodal imaging in frontotemporal degeneration
-
批准号:9069717
-
项目类别:
-
资助金额:$18.11万
-
财政年份:2013
-
负责人:HOWARD J ROSEN
-
依托单位:
Awareness of Deficits in Dementia
-
批准号:8079466
-
项目类别:
-
资助金额:$30.52万
-
财政年份:2010
-
负责人:HOWARD J ROSEN
-
依托单位:
Awareness of Deficits in Dementia
-
批准号:8484778
-
项目类别:
-
资助金额:$28.84万
-
财政年份:2010
-
负责人:HOWARD J ROSEN
-
依托单位:
Awareness of Deficits in Dementia
-
批准号:7888075
-
项目类别:
-
资助金额:$29.52万
-
财政年份:2010
-
负责人:HOWARD J ROSEN
-
依托单位:
The Frontotemporal Lobar Degeneration Neuroimaging Initiative
-
批准号:7939745
-
项目类别:
-
资助金额:$203.43万
-
财政年份:2009
-
负责人:HOWARD J ROSEN
-
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: