Functional Connectivity Network in default mode regions provides the underlying infrastructure for task-based functional co-de/activation networks
默认模式区域中的功能连接网络为基于任务的功能编码/激活网络提供底层基础设施
基本信息
- 批准号:10406379
- 负责人:
- 金额:$ 78.62万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-07-01 至 2024-04-30
- 项目状态:已结题
- 来源:
- 关键词:Alzheimer&aposs DiseaseAmyloidAmyloid beta-ProteinAnesthesia proceduresAttentionBlood flowBrainCharacteristicsCluster AnalysisCognitiveConsensusDataDevelopmentDiseaseEpisodic memoryEventExperimental DesignsFrequenciesFunctional Magnetic Resonance ImagingImaging TechniquesInfrastructureManuscriptsMapsMeasurementMeasuresMetabolicMetabolismMethodsNetwork-basedParticipantPositron-Emission TomographyProcessReportingRestRoleSensorySignal TransductionSleepSpecificitySpeedStructureSystemTask PerformancesTestingWorkage relatedbaseblood oxygenation level dependent responsecognitive taskfluorodeoxyglucose positron emission tomographyhealthy agingmetabolic ratemild cognitive impairmentneurophysiologynormal agingnovelpre-clinicalsensory stimulus
项目摘要
Summary
Recent developments demonstrate that the brain carries out its functions through a number of large-scale
functional sub-systems, or networks. One of the most studied brain networks is the default mode network
(DMN); however, the internal structure of the DMN, and how it carries out its functions, still remains elusive.
The topography of the DMN has been mapped using four different imaging techniques: through reductions in
the blood flow of DMN regions during task engagement using 15O-PET; as the hypermetabolic regions at rest
using FDG-PET; as the task-based deactivation using BOLD-fMRI; and through functional connectivity in
resting-state fMRI. The task-based blood-flow reductions observed in 15O-PET studies, and task-based
deactivations observed using BOLD-fMRI, seem to be reflective of the same neurophysiological processes,
since BOLD signal is highly confounded by blood flow. It has also been postulated that resting-state functional
connectivity and hypermetabolism in DMN regions reflect the same neurophysiological process; thus
concluding that the resting-state functional connectivity is the measurement of the brain’s baseline, intrinsic, or
resting-state activities. However, recent evidence has put such possibility under question by indicating that
resting-state functional connectivity networks are active during anesthesia, sleep, and even task-performance.
Such findings raise a critical, but as of yet unanswered, question: what is the role of such overlapping networks
in DMN regions? We hypothesize that functional connectivity in the DMN regions is representative of a lower
level process, which provides the underlying infrastructure for the higher-level network that carries out the
actual function.
Both functional connectivity and task-based deactivation in the DMN regions have been reported to be
disrupted with normal aging, the pre-clinical stage of Alzheimer’s disease, mild cognitive impairment and
Alzheimer’s disease. However, since the assumption in the field is that the DMN’s functional connectivity and
task-based deactivation are representative of the same underlying neurophysiological process, there has been
no study, to our knowledge, investigating the cascade of the events in which functional connectivity or negative
BOLD response get disrupted. Disentangling the cascade of events in the AD is crucial for understanding the
disease initiation, progress, and treatment. Our preliminary evidence in this project demonstrates that imposing
alteration in the task-based deactivation network does not have any effect on the functional connectivity of the
same regions. The current proposal will use asymptomatic stage of Alzheimer’s disease to test whether
disruption in the underlying functional connectivity results in any change to the task-based deactivations in the
DMN, which is an evidence for hierarchical structure.
摘要
最近的发展表明,大脑通过许多大规模的
正常运行的子系统或网络。研究最多的大脑网络之一是默认模式网络
然而,债务管理网络的内部结构及其如何履行其职能仍然令人费解。
DMN的地形是使用四种不同的成像技术绘制的:通过减少
以~(150)O-PET为静息高代谢区研究任务投入时DMN区的血流
使用FDG-PET;使用BOLD-fMRI作为基于任务的去激活;以及通过
静息状态功能磁共振成像。在15O-PET研究中观察到的基于任务的血流减少,以及基于任务的
使用BOLD-FMRI观察到的失活似乎反映了相同的神经生理过程,
因为大胆的信号与血液流动高度混淆。也有人假设静息状态的功能
DMN区域的连接和高代谢反映了相同的神经生理过程;因此
结论:静息状态的功能连通性是对大脑的基线、内在或
休息状态的活动。然而,最近的证据表明,这种可能性受到了质疑
静息状态的功能连接网络在麻醉、睡眠甚至任务执行期间都是活跃的。
这些发现提出了一个关键但尚未得到回答的问题:这种重叠网络的作用是什么
在DMN地区?我们假设DMN区域的功能连通性代表较低的
级别进程,为执行以下任务的更高级别网络提供底层基础设施
实际功能。
据报道,DMN区域的功能连接和基于任务的停用
与正常衰老、阿尔茨海默病临床前阶段、轻度认知障碍和
阿尔茨海默氏症。然而,由于现场的假设是DMN的功能连通性和
基于任务的去激活是相同的潜在神经生理过程的代表,已经有
据我们所知,没有研究调查功能连通性或负性事件的级联
大胆的回应被打乱了。理清AD中的一连串事件对于理解
疾病的始发、进展和治疗。我们在这个项目中的初步证据表明,强加
基于任务的去激活网络中的改变不会对
同样的地区。目前的提议将使用阿尔茨海默病的无症状阶段来测试
底层功能连接中断会导致对中基于任务的停用进行任何更改
DMN,这是等级结构的证据。
项目成果
期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Evidence suggesting common mechanisms underlie contralateral and ipsilateral negative BOLD responses in the human visual cortex.
- DOI:10.1016/j.neuroimage.2022.119440
- 发表时间:2022-11-15
- 期刊:
- 影响因子:5.7
- 作者:He H;Ettehadi N;Shmuel A;Razlighi QR
- 通讯作者:Razlighi QR
Attenuation of motion artifacts in fMRI using discrete reconstruction of irregular fMRI trajectories (DRIFT).
使用不规则 fMRI 轨迹离散重建 (DRIFT) 来衰减 fMRI 中的运动伪影。
- DOI:10.1002/mrm.28723
- 发表时间:2021
- 期刊:
- 影响因子:3.3
- 作者:Parker,DavidB;Spincemaille,Pascal;Razlighi,QolamrezaR
- 通讯作者:Razlighi,QolamrezaR
Landmark-guided region-based spatial normalization for functional magnetic resonance imaging.
- DOI:10.1002/hbm.25865
- 发表时间:2022-08-01
- 期刊:
- 影响因子:4.8
- 作者:
- 通讯作者:
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Qolamreza Ray Razlighi其他文献
Qolamreza Ray Razlighi的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Qolamreza Ray Razlighi', 18)}}的其他基金
Functional Connectivity Network in default mode regions provides the underlying infrastructure for task-based functional co-de/activation networks
默认模式区域中的功能连接网络为基于任务的功能编码/激活网络提供底层基础设施
- 批准号:
10203562 - 财政年份:2020
- 资助金额:
$ 78.62万 - 项目类别:
Functional Connectivity Network in default mode regions provides the underlying infrastructure for task-based functional co-de/activation networks
默认模式区域中的功能连接网络为基于任务的功能编码/激活网络提供底层基础设施
- 批准号:
10261530 - 财政年份:2020
- 资助金额:
$ 78.62万 - 项目类别:
Analyzing age-related changes of brain activation in subjects native space
分析受试者原生空间中与年龄相关的大脑激活变化
- 批准号:
9281626 - 财政年份:2013
- 资助金额:
$ 78.62万 - 项目类别:
Analyzing age-related changes of brain activation in subjects native space
分析受试者原生空间中与年龄相关的大脑激活变化
- 批准号:
8581477 - 财政年份:2013
- 资助金额:
$ 78.62万 - 项目类别:
Analyzing age-related changes of brain activation in subjects native space
分析受试者原生空间中与年龄相关的大脑激活变化
- 批准号:
8871510 - 财政年份:2013
- 资助金额:
$ 78.62万 - 项目类别:
Analyzing age-related changes of brain activation in subjects native space
分析受试者原生空间中与年龄相关的大脑激活变化
- 批准号:
9066053 - 财政年份:2013
- 资助金额:
$ 78.62万 - 项目类别:
Analyzing age-related changes of brain activation in subjects native space
分析受试者原生空间中与年龄相关的大脑激活变化
- 批准号:
8723048 - 财政年份:2013
- 资助金额:
$ 78.62万 - 项目类别:
相似国自然基金
新型F-18标记香豆素衍生物PET探针的研制及靶向Alzheimer's Disease 斑块显像研究
- 批准号:81000622
- 批准年份:2010
- 资助金额:20.0 万元
- 项目类别:青年科学基金项目
阿尔茨海默病(Alzheimer's disease,AD)动物模型构建的分子机理研究
- 批准号:31060293
- 批准年份:2010
- 资助金额:26.0 万元
- 项目类别:地区科学基金项目
跨膜转运蛋白21(TMP21)对引起阿尔茨海默病(Alzheimer'S Disease)的γ分泌酶的作用研究
- 批准号:30960334
- 批准年份:2009
- 资助金额:22.0 万元
- 项目类别:地区科学基金项目
相似海外基金
A Possible Association Between Insulin and Alzheimer?s Disease: Examining the Consequences of Altered Insulin Signalling on the Expression of Human Amyloid-Beta in Caenorhabditis elegans
胰岛素与阿尔茨海默氏病之间的可能关联:检查胰岛素信号改变对秀丽隐杆线虫中人类β淀粉样蛋白表达的影响
- 批准号:
428670 - 财政年份:2019
- 资助金额:
$ 78.62万 - 项目类别:
Studentship Programs
Nitration of Amyloid beta Alzheimer 's disease
β 淀粉样蛋白的硝化 阿尔茨海默病
- 批准号:
316914751 - 财政年份:2016
- 资助金额:
$ 78.62万 - 项目类别:
Research Grants
Effects of Latrepirdine on beta amyloid clearance, aggregation and neurodegeneration in Alzheimer�s disease
拉曲吡啶对阿尔茨海默病β淀粉样蛋白清除、聚集和神经变性的影响
- 批准号:
nhmrc : 1009295 - 财政年份:2011
- 资助金额:
$ 78.62万 - 项目类别:
NHMRC Project Grants
An investigation of the role of brain amyloid in cognition, brain atrophy and Alzheimer s disease in Down s syndrome
脑淀粉样蛋白在唐氏综合症认知、脑萎缩和阿尔茨海默病中作用的研究
- 批准号:
G1002252/1 - 财政年份:2011
- 资助金额:
$ 78.62万 - 项目类别:
Research Grant
DECREASED CLEARANCE OF CNS AMYLOID-? IN ALZHEIMER?S DISEASE
中枢神经系统淀粉样蛋白清除率降低?
- 批准号:
8361468 - 财政年份:2011
- 资助金额:
$ 78.62万 - 项目类别:
Studies of an early stage amyloid formation for Parkinson`s Disease casual protein.
帕金森病休闲蛋白的早期淀粉样蛋白形成的研究。
- 批准号:
20550083 - 财政年份:2008
- 资助金额:
$ 78.62万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Chemical crosslinking of helical form of amyloid-beta for the study of Alzheimer`s disease
β-淀粉样蛋白螺旋形式的化学交联用于阿尔茨海默氏病的研究
- 批准号:
318045-2005 - 财政年份:2005
- 资助金额:
$ 78.62万 - 项目类别:
Postgraduate Scholarships - Master's
In vivo imaging of beta-amyloid plaques in Alzheimer´s disease via positron emission tomography (PET)
通过正电子发射断层扫描 (PET) 对阿尔茨海默病中的 β-淀粉样斑块进行体内成像
- 批准号:
5405697 - 财政年份:2003
- 资助金额:
$ 78.62万 - 项目类别:
Research Grants
Functional studies on a neuroprotective activity of the amyloid precursor protein of Alzheimer s disease.
阿尔茨海默病淀粉样前体蛋白的神经保护活性的功能研究。
- 批准号:
nhmrc : 145761 - 财政年份:2001
- 资助金额:
$ 78.62万 - 项目类别:
NHMRC Project Grants
The neuroanatomy of Amyloid ß-Protein desposition in Alzheimer´s disease
阿尔茨海默病中淀粉样蛋白沉积的神经解剖学
- 批准号:
5326596 - 财政年份:2001
- 资助金额:
$ 78.62万 - 项目类别:
Research Grants














{{item.name}}会员




