Genetic and Epidemiological Predictors of Glucose Homeostasis Measures
血糖稳态措施的遗传和流行病学预测因子
基本信息
- 批准号:10088441
- 负责人:
- 金额:$ 65.2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-04-01 至 2024-01-31
- 项目状态:已结题
- 来源:
- 关键词:AffectAfrican AmericanAmericanArchitectureAsiansBeta CellBiologicalBiological ProcessCardiovascular DiseasesCase-Control StudiesCellular biologyClinicalClinical ManagementCollaborationsCommunitiesComplementComplexDataData SetDefectDetectionDiabetes MellitusDiagnosisDiseaseEarly DiagnosisEconomic BurdenEffectivenessEpidemiologyEuropeanEvaluationFunctional disorderFundingGenesGeneticGenetic DeterminismGenetic VariationGenetic studyGlucoseGoalsHeritabilityHispanicsHumanIndividualInsulin ResistanceInterventionLettersLinkage DisequilibriumMapsMeasuresMedical Care CostsMeta-AnalysisMethodologyMexicanMexican AmericansMinority GroupsModelingNatureNon-Insulin-Dependent Diabetes MellitusPatternPhenotypePhysiologicalPopulationPrediabetes syndromePreventionPublic HealthRecording of previous eventsReport (document)ResearchResourcesRiskSample SizeSamplingSouth AsianTestingTranslatingTranslationsVariantblood glucose regulationcase controlclinical phenotypeclinically relevantcohortdesigndiabetes riskgenome wide association studygenome-widehigh riskimprovedin silicoindexinginsightinsulin secretioninsulin sensitivitymetabolomicsmolecular phenotypemulti-ethnicmultiple omicsnext generation sequencingnovelrare variantresistance generisk predictionsuccesstrait
项目摘要
Summary
Insulin sensitivity and insulin secretion are traits that have a significant impact on the risk of type 2 diabetes
(T2D). The over-arching goal of this proposal is to understand the pathophysiology underlying variation of
these intermediate phenotypes in Mexican Americans, the largest US minority group and one at high risk of
T2D. The Genetics Underlying Diabetes in Hispanics (GUARDIAN) Consortium represents the largest effort to
identify the genetic determinants underlying diabetes-related intermediate phenotypes (DK085175). During the
previous funding period, genome-wide association studies (GWAS) focused on common genetic variation
identified four genome-wide significant loci underlying variation in glucose homeostasis traits which translated
to the clinical endpoint, T2D. In this application, we will build upon significant prior genetic findings with
integration of biological (metabolomics) and analytical (hierarchical clustering and interaction analysis)
approaches to further refine insulin resistance and insulin secretion phenotypes and explore their biological
basis. Aim 1 will develop a novel methodology using existing GWAS and metabolomics data to impute
genetically regulated metabolites (GReM) and test their association with measures of glucose homeostasis in
the GUARDIAN Consortium. Aim 2 will refine known and novel variants associated with T2D and related
phenotypes through hierarchical clustering and perform interaction analyses which exploit the bimodal nature
of T2D to identify additional insulin resistance loci. Aim 3 will identify genetic determinants of dynamic
measures of glucose homeostasis in diverse human populations and translate these loci to T2D. The unique
strengths of this proposal include detailed phenotypes for glucose homeostasis that have not been extensively
examined in the GWAS setting, a focus on the Mexican American population, and our long-standing, highly
productive collaborative team. This project has great public health significance as it is focused on increasing
our biological understanding and resultant mechanisms for the prevention of T2D using pre-diabetic measures
of glucose homeostasis.
总结
胰岛素敏感性和胰岛素分泌是对2型糖尿病风险有重大影响的性状
(T2D)。本提案的主要目标是了解以下变化的病理生理学
墨西哥裔美国人是美国最大的少数民族,也是最有可能患上癌症的人群之一。
2型糖尿病西班牙裔糖尿病遗传学基础(GUARDIAN)联盟代表了最大的努力,
确定糖尿病相关中间表型的遗传决定因素(DK085175)。期间
在上一个资助期,全基因组关联研究(GWAS)侧重于常见的遗传变异
确定了四个基因组范围内的显着位点的葡萄糖稳态性状的变化,翻译
临床终点T2D。在本申请中,我们将建立在重要的遗传学发现的基础上,
生物学(代谢组学)和分析(分层聚类和相互作用分析)的整合
进一步完善胰岛素抵抗和胰岛素分泌表型并探索其生物学特性的方法
基础目标1将开发一种新型方法,使用现有的GWAS和代谢组学数据来估算
遗传调节代谢物(GReM),并测试其与葡萄糖稳态的相关性,
守护者联盟目标2将细化与T2D相关的已知和新变体以及相关的
表型通过层次聚类和执行交互作用分析,利用双峰性质
以确定其他胰岛素抵抗基因座。目标3将确定动态的遗传决定因素
测量不同人群中的葡萄糖稳态,并将这些基因座转化为T2D。独特的
该建议的优点包括葡萄糖稳态的详细表型,
在GWAS环境中进行了检查,重点是墨西哥裔美国人,以及我们长期以来,高度重视
高效的协作团队。该项目具有重大的公共卫生意义,因为它的重点是增加
我们对使用糖尿病前期措施预防T2D的生物学理解和产生的机制
葡萄糖稳态的关键
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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Nicholette D. Allred其他文献
Nicholette D. Allred的其他文献
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{{ truncateString('Nicholette D. Allred', 18)}}的其他基金
Identification and Characterization of Loci Associated with Non-alcoholic Fatty Liver Disease
与非酒精性脂肪肝相关基因座的鉴定和表征
- 批准号:
10230705 - 财政年份:2021
- 资助金额:
$ 65.2万 - 项目类别:
Identification and Characterization of Loci Associated with Non-alcoholic Fatty Liver Disease
与非酒精性脂肪肝相关基因座的鉴定和表征
- 批准号:
10372217 - 财政年份:2021
- 资助金额:
$ 65.2万 - 项目类别:
Identification and Characterization of Loci Associated with Non-alcoholic Fatty Liver Disease
与非酒精性脂肪肝相关基因座的鉴定和表征
- 批准号:
10597023 - 财政年份:2021
- 资助金额:
$ 65.2万 - 项目类别:
Genetic and Epidemiological Predictors of Glucose Homeostasis Measures
血糖稳态措施的遗传和流行病学预测因子
- 批准号:
9902414 - 财政年份:2019
- 资助金额:
$ 65.2万 - 项目类别:
Genetic and Epidemiological Predictors of Glucose Homeostasis Measures
血糖稳态措施的遗传和流行病学预测因子
- 批准号:
10338054 - 财政年份:2019
- 资助金额:
$ 65.2万 - 项目类别:
Metabolomics of Neurocognitive Risk for Dementia in Diabetes
糖尿病痴呆神经认知风险的代谢组学
- 批准号:
10338066 - 财政年份:2019
- 资助金额:
$ 65.2万 - 项目类别:
Metabolomics of Neurocognitive Risk for Dementia in Diabetes
糖尿病痴呆神经认知风险的代谢组学
- 批准号:
10540341 - 财政年份:2019
- 资助金额:
$ 65.2万 - 项目类别:
Metabolomics of Neurocognitive Risk for Dementia in Diabetes
糖尿病痴呆神经认知风险的代谢组学
- 批准号:
10090550 - 财政年份:2019
- 资助金额:
$ 65.2万 - 项目类别:
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