Primary visual cortex plasticity following central vision loss
中央视力丧失后的初级视觉皮层可塑性
基本信息
- 批准号:8980362
- 负责人:
- 金额:$ 4.31万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2015
- 资助国家:美国
- 起止时间:2015-08-05 至 2017-08-04
- 项目状态:已结题
- 来源:
- 关键词:AffectAgeAge related macular degenerationAnatomyAreaAtrophicAttentionBlindnessBrain regionCellsCessation of lifeCognitiveDataDiseaseEducationElderlyFinancial compensationFunctional Magnetic Resonance ImagingGenderGoalsHealthImpairmentIndividualKnowledgeLearningMacular degenerationMediatingMindModalityModelingPaperParticipantPeer ReviewPeripheralPersonsPhasePopulationProcessPublicationsReadingResearchResearch EthicsResearch TrainingRetinaRetinalRetinal DiseasesRetinal PhotoreceptorsSchoolsStructureThickTissuesTrainingTraining ProgramsUnited StatesVisionVisualVisual CortexVisual FieldsVisual attentionWorkWritingage relatedarea striatacareer developmentexecutive functionexperienceextrastriate visual cortexfovea centralisfunctional plasticityinsightinterestmaculaneuroimagingpublic health relevancesymposiumvision sciencevisual informationvisual neuroscience
项目摘要
DESCRIPTION (provided by applicant): Age-related macular degeneration, a disease that affects nearly 2 million individuals in the United States, is characterized by the death of retinal
tissue in the macula, the area of the retina that mediates central vision. The resulting loss of cells often leads to profound deficits in visual function. However, many individuals with macular degeneration learn to use their spared peripheral vision for visual tasks such as reading, for which healthy vision participants would use the macula. It is unclear how the anatomy and function of structures beyond the retina contribute to this compensatory improvement in peripheral vision. This project's overall goal is to understand how primary visual cortex changes following this compensatory improvement in peripheral vision. Specifically, this study will investigate the structure and functional connections of primary visual cortex following central vision loss. To do this, we will use structural and functional Magnetic Resonance Imaging to investigate the cortex in participants with macular degeneration. These data will then be compared to age, gender, and education matched normally sighted controls. Our central hypothesis is that the structure (Aim 1) and functional connections (Aim 2) of primary visual cortex are modified after vision loss, in a way that is consistent with compensatory improvement in peripheral vision. These aims will be accomplished in the context of a formal training plan, sponsored by Drs. Kristina Visscher and Cynthia Owsley. This training plan includes research, coursework, and career development activities that will ultimately train me to be an independent cognitive neuroscientist. The research-training plan will focus on investigating the structural and
functional connections of primary visual cortex following central vision loss. The training plan wil also include coursework on visual neuroscience from the department of Vision Science as well as classes offered by the Graduate School on research ethics and writing scientific papers. Additionally, the training plan will have a focus on career development including: conference presentations, scientific writing in peer reviewed publications, and monthly discussions on how to prepare for the next state of my journey to becoming an independent cognitive neuroscientist.
描述(申请人提供):老年性黄斑变性是一种在美国影响近200万人的疾病,其特征是视网膜死亡
黄斑中的组织,视网膜中调节中央视觉的区域。由此导致的细胞损失往往会导致严重的视觉功能障碍。然而,许多黄斑变性患者学习使用他们多余的周边视觉来完成阅读等视觉任务,而健康的视力参与者会使用黄斑。目前尚不清楚视网膜以外结构的解剖和功能如何有助于周边视力的代偿性改善。该项目的总体目标是了解周边视力代偿性改善后初级视觉皮质的变化。具体地说,本研究将研究中枢视力丧失后初级视觉皮质的结构和功能联系。为此,我们将使用结构和功能磁共振成像来研究黄斑变性参与者的皮质。然后将这些数据与年龄、性别和教育程度相匹配的正常视力对照进行比较。我们的中心假设是,初级视觉皮质的结构(目标1)和功能连接(目标2)在视力丧失后发生改变,这与周围视力的代偿性改善是一致的。这些目标将在Kristina Visscher博士和Cynthia Owsley博士赞助的正式培训计划的背景下实现。这个培训计划包括研究、课程和职业发展活动,这些活动最终将把我培养成一名独立的认知神经学家。研究-培训计划将侧重于调查结构和
中枢视力丧失后初级视皮层的功能联系。培训计划还将包括视觉科学系的视觉神经科学课程,以及研究生院提供的研究伦理和撰写科学论文的课程。此外,培训计划将把重点放在职业发展上,包括:会议演讲、在同行评议出版物上发表科学文章,以及每月就如何准备成为一名独立认知神经学家的下一阶段进行讨论。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
数据更新时间:{{ journalArticles.updateTime }}
{{
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 }}
Wesley Burge其他文献
Wesley Burge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 }}
相似国自然基金
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
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
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
- 批准年份:2025
- 资助金额:0.0 万元
- 项目类别:省市级项目
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:
- 批准年份:2024
- 资助金额:0 万元
- 项目类别:面上项目
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
- 批准年份:2023
- 资助金额:0.0 万元
- 项目类别:省市级项目
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:
- 批准年份:2022
- 资助金额:33 万元
- 项目类别:地区科学基金项目
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:
- 批准年份:2022
- 资助金额:52 万元
- 项目类别:面上项目
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:n/a
- 批准年份:2022
- 资助金额:10.0 万元
- 项目类别:省市级项目
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
- 批准年份:2019
- 资助金额:55.0 万元
- 项目类别:面上项目
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
- 批准年份:2016
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
高血糖激活滑膜AGE-RAGE-PKC轴致骨关节炎易感的机制研究
- 批准号:81501928
- 批准年份:2015
- 资助金额:18.0 万元
- 项目类别:青年科学基金项目
相似海外基金
I(eye)-SCREEN: A real-world AI-based infrastructure for screening and prediction of progression in age-related macular degeneration (AMD) providing accessible shared care
I(eye)-SCREEN:基于人工智能的现实基础设施,用于筛查和预测年龄相关性黄斑变性 (AMD) 的进展,提供可及的共享护理
- 批准号:
10102692 - 财政年份:2024
- 资助金额:
$ 4.31万 - 项目类别:
EU-Funded
Inhibiting Neovascularization and Subretinal Fibrosis in Neovascular Age-Related Macular Degeneration
抑制新生血管性年龄相关性黄斑变性的新生血管形成和视网膜下纤维化
- 批准号:
10639785 - 财政年份:2023
- 资助金额:
$ 4.31万 - 项目类别:
Inhibition of melanogenesis in retinal pigment epithelium, a contributing factor in age-related macular degeneration
抑制视网膜色素上皮中的黑色素生成,这是年龄相关性黄斑变性的一个促成因素
- 批准号:
23K09052 - 财政年份:2023
- 资助金额:
$ 4.31万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
- 批准号:
10679287 - 财政年份:2023
- 资助金额:
$ 4.31万 - 项目类别:
Evaluation of New Anti-inflammatory Treatments for Age-Related Macular Degeneration
年龄相关性黄斑变性的新型抗炎治疗方法的评价
- 批准号:
10642988 - 财政年份:2023
- 资助金额:
$ 4.31万 - 项目类别:
Progression of Early Atrophic Lesions in Age-related Macular degeneration
年龄相关性黄斑变性早期萎缩性病变的进展
- 批准号:
10635325 - 财政年份:2023
- 资助金额:
$ 4.31万 - 项目类别:
Cellular and molecular mechanisms of AIM2 and NLRP3 inflammasome activation in age-related macular degeneration
年龄相关性黄斑变性中 AIM2 和 NLRP3 炎症小体激活的细胞和分子机制
- 批准号:
10584110 - 财政年份:2023
- 资助金额:
$ 4.31万 - 项目类别:
Elucidation of roles of mast cells and macrophages in the pathogenesis of age-related macular degeneration
阐明肥大细胞和巨噬细胞在年龄相关性黄斑变性发病机制中的作用
- 批准号:
22H03243 - 财政年份:2022
- 资助金额:
$ 4.31万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
AMD Mitochondria Modulate Expression of microRNA 135b-5p and 148a-3p in RPE Cybrids: Implications for Age-related Macular Degeneration
AMD 线粒体调节 RPE Cybrids 中 microRNA 135b-5p 和 148a-3p 的表达:对年龄相关性黄斑变性的影响
- 批准号:
10433610 - 财政年份:2022
- 资助金额:
$ 4.31万 - 项目类别:
Targeting the inflammatory response in age-related macular degeneration
针对年龄相关性黄斑变性的炎症反应
- 批准号:
10504138 - 财政年份:2022
- 资助金额:
$ 4.31万 - 项目类别: