Mass General Brigham HeartShare Clinical Center

麻省总医院布里格姆 HeartShare 临床中心

基本信息

  • 批准号:
    10679064
  • 负责人:
  • 金额:
    $ 28.38万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2021
  • 资助国家:
    美国
  • 起止时间:
    2021-09-10 至 2026-07-31
  • 项目状态:
    未结题

项目摘要

Project Summary Heart failure with preserved ejection fraction (HFpEF) comprises approximately half of all HF and is a highly morbid condition. Pharmacotherapies that are effective in treating HF with reduced ejection fraction have more modest if any beneficial impacts on HFpEF, potentially owing to heterogeneous definitions of HFpEF and limited understanding of optimal pathways to target in HFpEF. Our team of investigators has extensive experience in HFpEF human subjects research. Complementary Dyspnea and Heart Failure Evaluation Programs attract referral of HFpEF patients as well as dyspneic control patients without HFpEF to the Massachusetts General Hospital and Brigham and Women’s Hospital (“Mass General Brigham, MGB”). In addition, our team is highly engaged in assessing therapeutic interventions for HFpEF through robust clinical trials programs. The MGB HeartShare Team’s PIs are responsible for HFpEF clinical trial conceptualization, design, implementation, and endpoint adjudication via established core laboratories in echocardiography, cardiopulmonary exercise testing, advanced cardiovascular imaging, all of which could be used to support HeartShare. Our team also has expertise in working with MGB-based electronic health record data, population study data, and clinical trials that inform our understanding of HFpEF. Our group has used comprehensive cardiopulmonary exercise testing (CPET) to simultaneously quantitate invasive hemodynamics, blood gases, cardiac function, arterial tonometry and gas exchange patterns during exercise in individuals with conventionally defined HFpEF. We have begun to delineate contributions of impaired cardiac, pulmonary, vascular, and peripheral musculoskeletal reserve capacity that are not evident at rest. Our single-center HFpEF phenotyping study already consists of >700 patients with HFpEF subjected to uniform phenotyping (echocardiography, NT-proBNP, multi-site blood sampling at rest and with exercise and comprehensive CPET). In Aim 1 we will assemble a collaborative multidisciplinary investigative team capable of recruiting, phenotyping, and retaining ≥250 HFpEF patients in the HeartShare Program while also drawing from experience with core lab oversight, bioinformatic expertise in electronic medical record research, and leadership of network, population cohort, and clinical trial research relevant to HFpEF. In Aim 2 we will refine the diagnosis and subclassification of HFpEF through comprehensive clinical assessment including multi-modality imaging of cardiac structure and function, perturbational testing with exercise to probe multi-organ system physiologic reserve and longitudinal remote physiologic monitoring and assessment of frailty and cognition. We will also expand on our experience with creation of omics-based signatures of pathophysiologic states in HFpEF and deploy unsupervised machine learning approaches to the derived data. HeartShare will enhance understanding of HFpEF and our team is poised to translate improved understanding of HFpEF subtypes into new therapeutic intervention trials in HFpEF.
项目总结

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 }}

Akshay Suvas Desai其他文献

Akshay Suvas Desai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('Akshay Suvas Desai', 18)}}的其他基金

Mass General Brigham HeartShare Clinical Center
麻省总医院布里格姆 HeartShare 临床中心
  • 批准号:
    10483173
  • 财政年份:
    2021
  • 资助金额:
    $ 28.38万
  • 项目类别:
Mass General Brigham HeartShare Clinical Center
麻省总医院布里格姆 HeartShare 临床中心
  • 批准号:
    10327543
  • 财政年份:
    2021
  • 资助金额:
    $ 28.38万
  • 项目类别:

相似国自然基金

基于聚金属氧酸盐对Amyloid蛋白的定点化学修饰及其在阿尔茨海默症治疗中的应用
  • 批准号:
  • 批准年份:
    2020
  • 资助金额:
    63 万元
  • 项目类别:
    面上项目
基于S1P通路探究Amyloid-β在干性年龄相关性黄斑变性中的作用
  • 批准号:
    81870666
  • 批准年份:
    2018
  • 资助金额:
    57.0 万元
  • 项目类别:
    面上项目
Amyloid-beta-PirB 相互作用介导小胶质细胞表型和功能变化参与AD进展的机制研究
  • 批准号:
    81601123
  • 批准年份:
    2016
  • 资助金额:
    17.0 万元
  • 项目类别:
    青年科学基金项目
Beta-amyloid寡聚体特有的抗原表位多肽疫苗的研究
  • 批准号:
    30971012
  • 批准年份:
    2009
  • 资助金额:
    35.0 万元
  • 项目类别:
    面上项目
抗阿兹海默病Beta-Amyloid寡聚物单链可变区抗体的筛选及其动物试验
  • 批准号:
    30570622
  • 批准年份:
    2005
  • 资助金额:
    30.0 万元
  • 项目类别:
    面上项目

相似海外基金

The disease of 21 century: Development of a novel therapy for ATTR amyloidosis based on the pathogenesis of amyloid formation mechanism
21世纪的疾病:基于淀粉样蛋白形成机制的ATTR淀粉样变性新疗法的开发
  • 批准号:
    22K07528
  • 财政年份:
    2022
  • 资助金额:
    $ 28.38万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Amyloid Transcription Block Survival - Deriving Functionally Active Peptide Inhibitors of Amyloidosis and Toxicity
淀粉样蛋白转录阻断存活 - 衍生淀粉样变性和毒性的功能活性肽抑制剂
  • 批准号:
    2605106
  • 财政年份:
    2021
  • 资助金额:
    $ 28.38万
  • 项目类别:
    Studentship
Amyloid Transcription Block Survival - Deriving Functionally Active Peptide Inhibitors of Amyloidosis and Toxicity
淀粉样蛋白转录阻断存活 - 衍生淀粉样变性和毒性的功能活性肽抑制剂
  • 批准号:
    2598875
  • 财政年份:
    2021
  • 资助金额:
    $ 28.38万
  • 项目类别:
    Studentship
Analysis of cerebral amyloid angiopathy in hereditary ATTR amyloidosis
遗传性ATTR淀粉样变性脑淀粉样血管病分析
  • 批准号:
    21K15701
  • 财政年份:
    2021
  • 资助金额:
    $ 28.38万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Development of novel therapy for cardiac amyloidosis by identifying transthyretin-derived amyloid fibril deposition promoting factor
通过鉴定转甲状腺素蛋白衍生的淀粉样原纤维沉积促进因子开发心脏淀粉样变性的新疗法
  • 批准号:
    19K08493
  • 财政年份:
    2019
  • 资助金额:
    $ 28.38万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Study on the transmission of avian AA amyloidosis mediated by amyloid in the environment
淀粉样蛋白介导的禽类AA淀粉样变性在环境中的传播研究
  • 批准号:
    17K17702
  • 财政年份:
    2017
  • 资助金额:
    $ 28.38万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Establishing Strategies to Ameliorate Amyloid Pathology in Light Chain Amyloidosis
制定改善轻链淀粉样变性淀粉样蛋白病理学的策略
  • 批准号:
    10677553
  • 财政年份:
    2016
  • 资助金额:
    $ 28.38万
  • 项目类别:
Establishing Strategies to Ameliorate Amyloid Pathology in Light Chain Amyloidosis
制定改善轻链淀粉样变性淀粉样蛋白病理学的策略
  • 批准号:
    9270017
  • 财政年份:
    2016
  • 资助金额:
    $ 28.38万
  • 项目类别:
Establishing Strategies to Ameliorate Amyloid Pathology in Light Chain Amyloidosis
制定改善轻链淀粉样变性淀粉样蛋白病理学的策略
  • 批准号:
    10057800
  • 财政年份:
    2016
  • 资助金额:
    $ 28.38万
  • 项目类别:
Establishing Strategies to Ameliorate Amyloid Pathology in Light Chain Amyloidosis
制定改善轻链淀粉样变性淀粉样蛋白病理学的策略
  • 批准号:
    9104759
  • 财政年份:
    2016
  • 资助金额:
    $ 28.38万
  • 项目类别:
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了