Uncomplicating Diabetes: Reducing the Burden of Diabetes Related End-Organ Injury
缓解糖尿病并发症:减轻糖尿病相关终末器官损伤的负担
基本信息
- 批准号:9469452
- 负责人:
- 金额:$ 1.08万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-09-11 至 2018-08-31
- 项目状态:已结题
- 来源:
- 关键词:AddressAnimalsAreaBiologyBiotechnologyBlindnessBlood VesselsComplications of Diabetes MellitusDiabetes MellitusDiabetic AngiopathiesEnd stage renal failureFibrosisFutureGlucoseHearingHeart failureImpaired cognitionInflammationInjuryKnowledgeLeadLearningMolecularMorbidity - disease rateNew MexicoOrganOutcomePathologicPopulationRecruitment ActivityResearchResearch PersonnelScientistTimeTranslatingUpdateVascular remodelingangiogenesisdiabetes managementdiabeticimprovedinnovationmeetingsmortalitynon-diabeticnovelnovel therapeuticspremature atherosclerosispreventsymposium
项目摘要
ABSTRACT
Support is requested for a Keystone Symposia conference entitled Uncomplicating Diabetes: Reducing the
Burden of Diabetes Related End-Organ Injury, organized by Drs. Mark E. Cooper, Thomas M. Coffman,
Matthias G. von Herrath and Susan Quaggin. The conference will be held February 25 - March 1, 2018 in
Santa Fe, New Mexico.
This Keystone Symposia conference will address diabetic complications which remain the major cause of
morbidity and mortality in the diabetic population. Although the outlook has improved over the last two decades
with respect to diabetic vascular disease, these complications remain a major burden with the underlying
explanation for these complications at a molecular and cellular level as yet not fully clarified.
With recent advances in the management of diabetes, particularly new classes of glucose-lowering agents, it is
critical to determine if these new therapies have both glucose-dependent and independent effects in reducing
diabetes-related end-organ injury. With major advances in our understanding of key pathological features of
diabetic complications such as angiogenesis, fibrosis, inflammation and vascular remodeling, albeit in non-
diabetic contexts, now is the time to translate this new knowledge to the field of diabetic complications. By
learning from and recruiting such researchers into the field of diabetic complications, there is a great
opportunity to develop novel, highly innovative approaches to identify new targets in order to discover new
ways to treat, reverse or prevent diabetic complications that lead to premature atherosclerosis, heart failure,
blindness, cognitive impairment and end-stage renal disease.
摘要
要求支持一次题为“消除糖尿病并发症:减少糖尿病并发症”的Keystone专题讨论会。
糖尿病相关终末器官损伤的负担,由Mark E.库珀:托马斯M.科夫曼
马蒂亚斯湾冯·赫拉特和苏珊·奎金会议将于2018年2月25日至3月1日在
圣达菲,新墨西哥州。
本次Keystone研讨会将讨论糖尿病并发症,这仍然是糖尿病的主要原因。
糖尿病人群的发病率和死亡率。尽管在过去的二十年里,
对于糖尿病血管疾病,这些并发症仍然是潜在的主要负担,
在分子和细胞水平上对这些并发症的解释尚未完全澄清。
随着糖尿病管理的最新进展,特别是新型降糖药,
关键是要确定这些新疗法是否具有葡萄糖依赖性和独立的作用,
糖尿病相关的终末器官损伤随着我们对心脏病的关键病理特征的理解的重大进展,
糖尿病并发症,如血管生成、纤维化、炎症和血管重塑,尽管在非糖尿病患者中,
糖尿病背景下,现在是时候把这个新的知识转化为糖尿病并发症领域。通过
从这些研究人员那里学习并招募他们进入糖尿病并发症领域,
有机会开发新的,高度创新的方法来确定新的目标,以发现新的
治疗、逆转或预防导致过早动脉粥样硬化、心力衰竭
失明、认知障碍和终末期肾病。
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)
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Thale Cross Jarvis其他文献
Thale Cross Jarvis的其他文献
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{{ truncateString('Thale Cross Jarvis', 18)}}的其他基金
Autophagy and Neurodegeneration: Mechanisms to Therapies
自噬和神经退行性变:治疗机制
- 批准号:
10608666 - 财政年份:2023
- 资助金额:
$ 1.08万 - 项目类别:
Malaria: Confronting Challenges From Drug Discovery to Treatment
疟疾:面临从药物发现到治疗的挑战
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10468493 - 财政年份:2022
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Modern Phenotypic Drug Discovery: From Chemical Biology to Therapeutics
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- 批准号:
10468419 - 财政年份:2022
- 资助金额:
$ 1.08万 - 项目类别:
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