Stented Artery Wall Stresses and Retenosis
支架动脉壁应力和再狭窄
基本信息
- 批准号:6995218
- 负责人:
- 金额:$ 33.54万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2003
- 资助国家:美国
- 起止时间:2003-03-01 至 2008-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
DESCRIPTION (provided by applicant): Balloon angioplasty and stenting are techniques for treating atherosclerosis that are increasing in use. Unfortunately, there is a 20-30% risk of a new blockage developing in the treated artery. Restenosis of vascular stents may be related to the mechanical conditions that they create. Recent investigations in stented vessels revealed a complex flow field including large-scale vortices and flow stagnation between the struts. Abnormally high solid wall stress concentrations have also been predicted at the proximal and distal ends of the stent. The chronic force of the stent against the artery also restricts it from experiencing normal, physiologic deformation. Based on previous studies of artery wall responses to similar changes in the mechanical environment, it is reasonable to expect that this aspect of stenting influences restenosis. Although stent design is crucial in creating mechanical phenomena known to be damaging to arteries, little attention has been given to the effects on stent failure, and ways to improve stent performance through better design. The research outlined in this proposal is based on the hypothesis that mechanical phenomena are, in part, responsible for clinical failures of vascular stents. The Specific Aims of this research include the construction of realistic mechanical models of stented arteries using computational techniques. The stent structure will be optimized to minimize stress on the artery wall, while maximizing the amount of normal, physiologic deformation. Carefully designed animal studies will provide confirmation of the importance of mechanical factors in inflammatory response. The long-term goal is to use this information to help develop the next generation of stents in which the role of arterial mechanics is a prime consideration.
描述(由申请人提供):球囊血管成形术和支架植入术是用于治疗动脉粥样硬化的技术,其使用越来越多。不幸的是,有20-30%的风险在治疗的动脉中形成新的阻塞。血管支架的恢复可能与其产生的机械条件有关。最近在支架血管中的研究揭示了复杂的流场,包括大尺度涡流和支柱之间的流动停滞。在支架的近端和远端也预测了异常高的固体壁应力集中。支架对动脉的慢性力也限制了其经历正常的生理变形。基于先前对动脉壁对机械环境中类似变化的反应的研究,可以合理预期支架植入术的这一方面会影响再狭窄。尽管支架设计在产生已知会损害动脉的机械现象方面至关重要,但很少关注对支架失效的影响以及通过更好的设计改善支架性能的方法。本提案中概述的研究基于以下假设:机械现象是血管支架临床失效的部分原因。本研究的具体目的包括使用计算技术构建支架动脉的真实力学模型。将优化支架结构,以最大限度地减少动脉壁上的应力,同时最大限度地增加正常生理变形量。精心设计的动物研究将证实机械因素在炎症反应中的重要性。长期目标是利用这些信息来帮助开发下一代支架,其中动脉力学的作用是首要考虑因素。
项目成果
期刊论文数量(9)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Mechanical modeling of stents deployed in tapered arteries.
- DOI:10.1007/s10439-008-9582-0
- 发表时间:2008-12
- 期刊:
- 影响因子:3.8
- 作者:Timmins, Lucas H.;Meyer, Clark A.;Moreno, Michael R.;Moore, James E., Jr.
- 通讯作者:Moore, James E., Jr.
Increased artery wall stress post-stenting leads to greater intimal thickening.
- DOI:10.1038/labinvest.2011.57
- 发表时间:2011-06
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
Deformation-induced hydrolysis of a degradable polymeric cylindrical annulus.
- DOI:10.1007/s10237-009-0168-z
- 发表时间:2010-04
- 期刊:
- 影响因子:3.5
- 作者:Soares, Joao S.;Rajagopal, Kumbakonam R.;Moore, James E., Jr.
- 通讯作者:Moore, James E., Jr.
Biomechanical issues in endovascular device design.
- DOI:10.1583/08-2605.1
- 发表时间:2009-02
- 期刊:
- 影响因子:0
- 作者:Moore JE Jr
- 通讯作者:Moore JE Jr
{{
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 }}
JAMES E MOORE其他文献
JAMES E MOORE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('JAMES E MOORE', 18)}}的其他基金
Lymphatic Fluid Flow Modeling with Active Network Components
使用主动网络组件进行淋巴液流动建模
- 批准号:
7918903 - 财政年份:2009
- 资助金额:
$ 33.54万 - 项目类别:
Lymphatic Fluid Flow Modeling with Active Network Components
使用主动网络组件进行淋巴液流动建模
- 批准号:
7687313 - 财政年份:2009
- 资助金额:
$ 33.54万 - 项目类别:
Lymphatic Fluid Flow Modeling with Active Network Components
使用主动网络组件进行淋巴液流动建模
- 批准号:
8123190 - 财政年份:2009
- 资助金额:
$ 33.54万 - 项目类别:
相似国自然基金
卡路里限制的T细胞糖脂代谢重塑机制及网络调控
- 批准号:91957111
- 批准年份:2019
- 资助金额:80.0 万元
- 项目类别:重大研究计划
高尿酸血症促进动脉粥样硬化机制探讨
- 批准号:81170251
- 批准年份:2011
- 资助金额:14.0 万元
- 项目类别:面上项目
磷脂转运蛋白通过磷酸鞘氨醇1影响高密度脂蛋白抗动脉粥样硬化功能的分子机制
- 批准号:81070247
- 批准年份:2010
- 资助金额:33.0 万元
- 项目类别:面上项目
大麻素CB2受体:巨噬细胞efferocytosis功能调控和不稳定斑块防治的新靶点
- 批准号:81000086
- 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
抑制PI3K/Akt/mTOR/p70S6K 信号通路促进巨噬细胞自体吞噬稳定易损斑块的分子机制研究
- 批准号:30971216
- 批准年份:2009
- 资助金额:31.0 万元
- 项目类别:面上项目
基因缺失突变抑制白细胞趋化稳定动脉粥样硬化易损斑块的研究
- 批准号:30871040
- 批准年份:2008
- 资助金额:32.0 万元
- 项目类别:面上项目
相似海外基金
Targeted ablation of cerebral atherosclerosis using supramolecular self-assembly
利用超分子自组装靶向消融脑动脉粥样硬化
- 批准号:
24K21101 - 财政年份:2024
- 资助金额:
$ 33.54万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
Contribution of Endothelial Planar Cell Polarity pathways in Blood Flow Direction Sensing
内皮平面细胞极性通路在血流方向传感中的贡献
- 批准号:
10750690 - 财政年份:2024
- 资助金额:
$ 33.54万 - 项目类别:
Colchicine for the prevention of vascular events after an acute intracerebral hemorrhage (CoVasc-ICH)
秋水仙碱用于预防急性脑出血后血管事件(CoVasc-ICH)
- 批准号:
485530 - 财政年份:2023
- 资助金额:
$ 33.54万 - 项目类别:
Operating Grants
Identifying the Role of Sex Hormones in Carotid Atherosclerotic Plaque Instability
确定性激素在颈动脉粥样硬化斑块不稳定中的作用
- 批准号:
494557 - 财政年份:2023
- 资助金额:
$ 33.54万 - 项目类别:
Operating Grants
Body composition and atherosclerosis-related biomarkers in women with endometriosis
子宫内膜异位症女性的身体成分和动脉粥样硬化相关生物标志物
- 批准号:
23K15842 - 财政年份:2023
- 资助金额:
$ 33.54万 - 项目类别:
Grant-in-Aid for Early-Career Scientists
Targeted multimodal stimuli-responsive nanogels for atherosclerosis imaging and therapy
用于动脉粥样硬化成像和治疗的靶向多模式刺激响应纳米凝胶
- 批准号:
2880683 - 财政年份:2023
- 资助金额:
$ 33.54万 - 项目类别:
Studentship
The Epigenetic Regulator Prdm16 Controls Smooth Muscle Phenotypic Modulation and Atherosclerosis Risk
表观遗传调节因子 Prdm16 控制平滑肌表型调节和动脉粥样硬化风险
- 批准号:
10537602 - 财政年份:2023
- 资助金额:
$ 33.54万 - 项目类别:
Role of IL-6 trans signaling in atherosclerosis development and late-stage pathogenesis
IL-6反式信号传导在动脉粥样硬化发展和晚期发病机制中的作用
- 批准号:
10652788 - 财政年份:2023
- 资助金额:
$ 33.54万 - 项目类别:
Whole genome sequence interpretation for lipids to discover new genes and mechanisms for coronary artery disease
脂质的全基因组序列解释,以发现冠状动脉疾病的新基因和机制
- 批准号:
10722515 - 财政年份:2023
- 资助金额:
$ 33.54万 - 项目类别:














{{item.name}}会员




