The TEDDY Study: Georgia/Florida Clinical Center
The TEDDY Study: Georgia/Florida Clinical Center
批准号:
8511114
负责人:
JIN-XIONG SHE
金额:
$531.93万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-03-01 至 2018-05-31
关键词:
15 year old4 year oldAddressAffectAgeAncillary StudyAutoantibodiesAutoimmune DiseasesAutoimmunityBiologicalBiological MarkersBirthCeliac DiseaseChildChild DevelopmentClinicalCohort StudiesCollaborationsColoradoCommunitiesContractsCountryDNADataData Coordinating CenterDevelopmentDiabetes MellitusDiagnosisDietary FactorsDiseaseEnrollmentEnvironmentEnvironmental ExposureEnvironmental Risk FactorEpidemiologyEthnic OriginEtiologyEuropeEventFecesFinlandFloridaFundingGenderGenesGeneticGenetic PolymorphismGenotypeGermanyGoalsHLA-DR AntigensInfantInfectionInfectious AgentInsulinInsulin-Dependent Diabetes MellitusLaboratoriesMonitorNational Institute of Diabetes and Digestive and Kidney DiseasesNested Case-Control StudyNewborn InfantOutcome StudyParticipantPathogenesisPerformancePeripheral Blood Mononuclear CellPlasmaPreventionProtocols documentationPublishingRNAResearch DesignResearch PersonnelResolutionResourcesRiskRisk EstimateSamplingScientistSpecimenSwedenTestingTimeUnited StatesUnited States National Institutes of HealthWashingtonWorkcohortdesigndiabetes riskendocrine pancreas developmentfollow-upgene environment interactionhigh riskimprovedinfancyinsightisletnovelpreventprospectivepublic health relevancerepositorytime use
中文摘要
描述(由申请人提供):年轻人糖尿病的环境决定因素(TEDDY)研究于2003年由美国和欧洲的六个临床中心发起,包括我们,以确定可能引发或防止胰岛自身免疫和1型糖尿病(T1 D)发展的感染因子,饮食因素或其他环境暴露。其他长期科学目标包括评估影响胰岛自身免疫或T1 D发展的潜在基因-环境相互作用,深入了解机制,并与更广泛的科学界分享收集的标本,以研究T1 D发病机制和预防。共有424,788名新生儿接受了HLA-DR,DQ基因分型筛查,以确定T1 D风险增加的儿童,8677名新生儿每年随访4次,直至4岁,此后每年随访2次,直至15岁。我们的临床中心已招募了965名TEDDY参与者;截至2012年6月30日,其中35名已出现持续确认的胰岛自身抗体,6名已被诊断为T1 D。我们的多中心前瞻性队列研究的更新申请的具体目的是:1)对8677名胰岛自身免疫、糖尿病和乳糜泻高危儿童的TEDDY队列进行5年以上随访; 2)根据标准TEDDY方案收集所有计划的生物样本和流行病学数据,包括密切监测性能以及样本和数据的质量; 3)在适当的时间进行计划的实验室测试,使用巢式病例对照研究设计来回答与TEDDY研究目标相关的特定科学问题和假设; 4)与TEDDY数据协调中心合作分析和发布实验室和流行病学数据(单独供资),和5)通过临床中心研究者和工作人员参与研究指导委员会和小组的工作,指导正在进行的TEDDY项目。委员会。一个成功的研究结果应该允许更好地了解胰岛自身免疫和T1 D的病因和发病机制,并开发新的策略来预防,延迟或逆转疾病。
英文摘要
DESCRIPTION (provided by applicant): The Environmental Determinants of Diabetes in the Young (TEDDY) study was initiated in 2003 by six clinical centers in the United States and Europe, including ours, to identify infectious agents, dietary factors, or other environmental exposures that may trigger or protect against the development of islet autoimmunity and type 1 diabetes (T1D). Additional long-term scientific goals include assessment of potential gene-environment interactions affecting development of islet autoimmunity or T1D, gaining insight on mechanisms, and sharing collected specimens with broader scientific community for studies of T1D pathogenesis and prevention. A total of 424,788 newborns have been screened by HLA-DR, DQ genotyping to identify children at increased risk for T1D and 8677 are followed four times a year until 4 years of age and twice a year thereafter until age 15. Our Clinical Center has enrolled 965 TEDDY participants; of those 35 have developed persistent confirmed islet autoantibodies and 6 have been diagnosed with T1D, as of 6/30/2012. The specific aims of this renewal application for our multi-center, prospective cohort study are to: 1) Follow the TEDDY cohort of 8677 high-risk children for development of islet autoimmunity and diabetes and celiac disease for 5 more years; 2) Collect all planned biological specimens and epidemiological data according to the standard TEDDY protocol including close monitoring of performance and of the quality of samples and data; 3) Perform planned laboratory tests at appropriate times using a nested case-control study design to answer specific scientific questions and hypotheses pertinent to the TEDDY study goals; 4) Analyze and publish laboratory and epidemiological data in collaboration with the TEDDY Data Coordinating Center (funded separately), and 5) Guide the ongoing TEDDY project by participation of the Clinical Center investigators and staff in work of the study Steering Committee and sub-committees. A successful study outcome should allow better understanding of the etiology and pathogenesis of islet autoimmunity and T1D and the development of new strategies to prevent, delay, or reverse the disease.
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