Type 1 Diabetes TrialNet: Clinical Centers (U01)
Type 1 Diabetes TrialNet: Clinical Centers (U01)
批准号:
8288865
负责人:
PHILIP RASKIN
金额:
$49.21万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-30 至 2014-04-30
关键词:
AddressAdverse effectsAffectAmputationAnti-Inflammatory AgentsAnti-inflammatoryBeta CellBlindnessCell physiologyChildClinicalClinical TrialsComplications of Diabetes MellitusCost SavingsDevelopmentDiabetes MellitusDiseaseDrug usageGoalsHealth Care CostsHumanImmuneIndividualInsulinInsulin-Dependent Diabetes MellitusInterventionIslets of LangerhansKidney FailureLife StyleMediatingPharmaceutical PreparationsPioglitazonePreventionPropertyProtocols documentationRegulatory T-LymphocyteResearchSavingsSeriesT-LymphocyteTestingToxic effectUnited StatesWorkbasedesigndiabetic patientexperienceimmunoregulationinnovationinsulin secretionpatient populationpreventpublic health relevanceresponsesuccesstherapy designyoung adult
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Type 1 diabetes affects more than one million individuals, mostly children and young adults, in the United States and many more worldwide. It occurs in genetically predisposed individuals as a consequence of immune-mediated destruction of the pancreatic islet insulin-secreting beta cells. The present treatment for Type 1 diabetes, when implemented properly, can delay or prevent the long-term complications of diabetes (i.e., blindness, renal failure, and amputation). However, proper diabetes treatment is quite difficult to do, expensive, and very invasive to the diabetic patient's lifestyle. Diabetes is also a major factor in health care costs. Is it possible to prevent Type 1 diabetes or to preserve insulin secretion once diabetes has develped? Several immune interventions have been tried in genetically susceptible individuals without success. Other trials have been attempted to intervene early in the course of Type 1 diabetes, in order to preserve beta cell function. These immune interventions using drugs with potential toxicity have failed. Thus, the identification of agents which either prevent the disease or slow its progression would result in major health care cost savings and reduce complications related to diabetes in addition to the huge individual savings in terms of not having the disease. Our long-term goal is to prevent the development of Type 1 diabetes through the use of innovative based therapies designed to prevent the development of the disease in genetically predisposed individuals. The objectives of this application, in pursuit of that goal and in response to the RFA, is completion of the TrialNet protocols and to continue to develop and test innovative interventions to prevent or slow the progression of Type 1 diabetes. One such innovative approach to slow the progression of Type 1 diabetes is our proposed protocol, "Pioglitazone Preserves Insulin Secretion in Type 1 Diabetes." The proposed work is innovative because it utilitizes a drug that is in wide spread use with low toxicity yet has immunomodulation and anti- inflamatory properties. We have also designed a series of mechanistic studies to examine whether the anti-inflammatory properties of the drug operate by influencing regulatory T-cells.
PUBLIC HEALTH RELEVANCE: The significance of this research is that the prevention of type 1 diabetes will save millions of dollars and enormous human suffering. The identification of agents which either prevent the disease or slow its progression would result in major health care cost savings and reduce complications related to diabetes in addition to the huge individual savings in terms of not having the disease.
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Type 1 Diabetes TrialNet: Clinical Centers (U01)
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批准号:8468689
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项目类别:
-
资助金额:$54.78万
-
财政年份:2009
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负责人:PHILIP RASKIN
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依托单位:
Type 1 Diabetes TrialNet: Clinical Centers (U01)
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批准号:7784271
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项目类别:
-
资助金额:$63.52万
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财政年份:2009
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负责人:PHILIP RASKIN
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依托单位:
Type 1 Diabetes TrialNet: Clinical Centers (U01)
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批准号:8073474
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项目类别:
-
资助金额:$62.52万
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财政年份:2009
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负责人:PHILIP RASKIN
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依托单位:
Type 1 Diabetes TrialNet: Clinical Centers (U01)
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批准号:7938971
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项目类别:
-
资助金额:$66.2万
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财政年份:2009
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负责人:PHILIP RASKIN
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依托单位:
NATURAL HISTORY STUDY OF THE DEVELOPMENT OF TYPE 1 DIABETES
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批准号:7377645
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项目类别:
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资助金额:$0.06万
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财政年份:2006
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负责人:PHILIP RASKIN
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依托单位:
TO COMPARE THE RELIABILITY OF MMTT AND IV GLUCAGON STIMULATION TEST
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批准号:7377649
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项目类别:
-
资助金额:$0.03万
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财政年份:2006
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负责人:PHILIP RASKIN
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依托单位:
PROLONGED HYPERGLYCEMIA EFFECTS ON INSULIN SECRETION IN DIABETES
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批准号:7206029
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项目类别:
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资助金额:$1.06万
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财政年份:2005
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负责人:PHILIP RASKIN
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依托单位:
Pathophysiology of Ketosis-Prone Diabetes in Obese Adults
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批准号:6975043
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项目类别:
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资助金额:$1.68万
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财政年份:2004
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负责人:PHILIP RASKIN
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依托单位:
Prolonged hyperglycemia effects on insulin secretion in diabetes
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批准号:6975096
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项目类别:
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资助金额:$1.62万
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财政年份:2004
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负责人:PHILIP RASKIN
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依托单位:
Diabetes Prevention Trial - Type I Diabetes (DPT-1)
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批准号:6975042
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项目类别:
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资助金额:$0.33万
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财政年份:2004
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负责人:PHILIP RASKIN
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依托单位:
DPT-1 TrialNet: Clinical Centers
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批准号:6660351
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项目类别:
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资助金额:$31.1万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
CLINICAL EVALUATION OF GLUCOSE MICROELECTRODES
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批准号:6567654
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项目类别:
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资助金额:$32.14万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
Diabetes type 1 TrialNet: Clinical Centers
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批准号:6442661
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项目类别:
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资助金额:$30.93万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
DIABETES PREVENTION TRIAL--TYPE I DIABETES (DPT 1)
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批准号:6567674
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项目类别:
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资助金额:$32.14万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
DPT-1 TrialNet: Clinical Centers
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批准号:7109257
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项目类别:
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资助金额:$0.0万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
DPT-1 TrialNet: Clinical Centers
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批准号:6798762
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项目类别:
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资助金额:$31.92万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
GLUCAGON SECRETION IN WELL CONTROLLED DIABETES MELLITUS
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批准号:6567632
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项目类别:
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资助金额:$32.14万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
ACUTE GLUCOSE DISPOSAL POST INTRAVENOUS GLUCOSE LOAD
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批准号:6567699
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项目类别:
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资助金额:$32.14万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
Diabetes Type 1 TrialNet: Clinical Centers
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批准号:7285682
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项目类别:
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资助金额:$66.92万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
DPT-1 TrialNet: Clinical Centers
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批准号:6927168
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项目类别:
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资助金额:$36.51万
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财政年份:2001
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负责人:PHILIP RASKIN
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依托单位:
海外基金