Uncomplicating Diabetes: Reducing the Burden of Diabetes Related End-Organ Injury
Uncomplicating Diabetes: Reducing the Burden of Diabetes Related End-Organ Injury
批准号:
9469452
负责人:
Thale Cross Jarvis
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
项目状态:
已结题
起止时间:
2017-09-11 至 2018-08-31
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
中文摘要
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英文摘要
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.
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