Vitamin D and Cardiovascular Disease
Vitamin D and Cardiovascular Disease
批准号:
7614118
负责人:
RAVI THADHANI
金额:
$1.0万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-15 至 2009-09-14
关键词:
AreaBasic ScienceBindingBiologicalBiologyBostonCardiac MyocytesCardiologyCardiovascular DiseasesCardiovascular systemCellsClinicalClinical ResearchCollaborationsConsensusDataDiseaseEndothelial CellsEtiologyEventFoundationsGeneral HospitalsGenetic TranscriptionGoalsHealthHormonesHospitalsJournalsKidneyKnowledgeLinkMainstreamingMassachusettsNuclearParathyroid glandPathway interactionsPatientsPhaseProcessPublicationsPublishingReceptor ActivationResearchResearch PersonnelScientistSmooth MuscleTherapeuticTranslatingTubular formationUnderrepresented MinorityVitamin DVitamin D DeficiencyVitamin D3 ReceptorWomanWorkcardiovascular disorder therapycell typedayexperiencegastrointestinal epitheliumkidney cellmacrophagenovelposterssymposium
中文摘要
描述(由申请人提供):
维生素D缺乏和心血管疾病(CVD)都是非常普遍的疾病。虽然对CVD的病因和治疗了解很多,但关于维生素D对心血管的影响的数据很少。几十年来,人们已经知道维生素D(25(OH)D3)通过肾脏转化为活性激素1,25(OH)2D 3。一旦转化,1,25(OH)2D 3能够与多种细胞类型(包括肠上皮细胞、甲状旁腺细胞和肾小管细胞)中的核维生素D受体(VDR)结合,并随后进行特异性基因转录。然而,最近,已经变得明显的是,VDR存在于其他关键细胞类型中,包括巨噬细胞、平滑肌和内皮细胞以及心肌细胞。这些数据支持维生素D参与心血管健康。虽然这一主题尚未成为CVD研究的主流,但新兴的生物学和临床联系表明,维生素D和CVD专家之间加强合作可能会产生新的CVD研究和潜在疗法。我们的目标是制定一份共识文件,强调维生素D和CVD之间的生物学和临床证据,以及为各种形式的CVD患者提供维生素D治疗的潜在研究策略。为了实现这一目标,来自美国各地的著名维生素D和心血管疾病专家和有前途的年轻研究人员将于2008年10月聚集在波士顿参加为期一天半的题为维生素D和心血管疾病的全国研讨会。我们的目标是:1。批判性地研究现有的基础科学和临床证据,将维生素D缺乏症与心血管疾病联系起来; 2。研究导致CVD的新途径,并确定这些过程如何与VDR激活的生长生物学联系起来; 3.定义维生素D生物学如何转化为临床研究和CVD患者的潜在治疗选择。据我们所知,这次拟议的研讨会将是第一次将维生素D和CVD联系起来。本次专题讨论会将主要由NHLBI提供支持,并对所有剩余的支持做出了强有力的机构承诺。重要的是,我们将邀请(并支付费用)来自美国各地的20名年轻科学家在这次研讨会上介绍他们的工作(口头和海报)。研讨会将在马萨诸塞州总医院的校园内举行,我们预计将有75名来自美国各地的与会者,有特殊需要的人将得到适当的安置。本提案的主要研究者和合作研究者指导医院的D受体激活研究中心(CeDAR),并在该领域发表了大量文章。此外,它们过去在有效规划和举办高质量的类似专题讨论会方面有经验,并成功地编写了供出版的协商一致文件。在该提案的所有阶段(规划、发言人、工作组),妇女和代表不足的少数民族都有很好的代表性,共识文件将发表在一本著名的心脏病学杂志上。最后,本次研讨会将为在波士顿会议后18-24个月内在全国心脏病学会议上规划和提议更大的会议提供基础;本次会议将得到CeDAR的支持。
英文摘要
DESCRIPTION (provided by applicant):
Both vitamin D deficiency and cardiovascular disease (CVD) are highly prevalent disorders. Although much is known about the etiology and treatment of CVD, there are sparse data on the cardiovascular effects of vitamin D. For decades, it has been known that Vitamin D (25(OH)D3) is converted to the active hormone 1,25(OH)2D3 by the kidney. Once converted, 1,25(OH)2D3 is capable of binding to the nuclear vitamin D receptor (VDR) in a variety of cell types including the gut epithelia, parathyroid cells, and kidney tubular cells, and specific gene transcription follows. More recently, however, it has become apparent that the VDR exists in other critical cell types including macrophages, smooth muscle and endothelial cells, and cardiac myocytes. These data support the involvement of vitamin D in cardiovascular health. Although the topic is not yet in the mainstream of CVD research, the emerging biological and clinical links suggest novel research and potential therapies for CVD that may emerge from stronger collaborations between Vitamin D and CVD experts. Our goal is to develop a consensus document highlighting the biological and clinical evidence linking vitamin D and CVD, and potential research strategies for bringing vitamin D therapies to patients with various forms of CVD. To accomplish this goal, renowned Vitamin D and CVD experts and promising young investigators from throughout the US will converge in Boston for a 1.5-day national symposium entitled Vitamin D and Cardiovascular Disease in October, 2008. Our objectives will be to: 1. To critically examine the existing basic science and clinical evidence linking vitamin D deficiency and CVD; 2. To examine novel pathways leading to CVD, and to determine how these processes may be linked with the growing biology of VDR activation; 3. To define how vitamin D biology can be translated to clinical studies and potential therapeutic options for patients with CVD. To our knowledge, this proposed symposium will be the first of its kind to link Vitamin D and CVD. This symposium will be primarily supported by NHLBI, and there is strong institutional commitment for all the remaining support. Importantly, we will invite (and pay expenses for) 20 young scientists from throughout the US to present their work (orally and by posters) at this symposium. The symposium will take place on the campus of the Massachusetts General Hospital, we expect 75 attendees from throughout the US, and those with special needs will be appropriately accommodated. The PI and Co-Investigator of this proposal direct the hospital's Center for D-receptor Activation Research (CeDAR), and have published extensively in this area. Moreover, they have past experience in efficiently planning and implementing similar symposia of high quality, and they have successfully developed consensus documents for publication. There is excellent representation of women and under-represented minorities in all phases of this proposal (Planning, Speakers, Working Group), and the consensus document will be published in a prominent cardiology journal. Finally, this symposium will provide the foundation for planning and proposing a larger meeting at a national cardiology meeting within 18-24 months of the Boston event; this event will be supported by CeDAR.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Support of the Emory National Primate Research Center
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海外基金