Skeletal Regulation of Cortical and Trabecular Bone by Parathyroid Hormone
Skeletal Regulation of Cortical and Trabecular Bone by Parathyroid Hormone
批准号:
8352466
负责人:
Natalie Cusano
金额:
$18.36万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-07-01 至 2017-04-30
关键词:
AffectBiochemicalBiochemical MarkersBiochemical PathwayBone DensityBone ResorptionCellsCharacteristicsDatabasesDevelopmentDiseaseDisease of parathyroid glandsDistalDoseExposure toFinite Element AnalysisGoalsHormonesHyperparathyroidismHypoparathyroidismIndividualInterventionKnowledgeLeadLinkMediatingMetabolicMetabolismMineralsModelingOsteoblastsOsteoclastsOsteoporosisParathyroid glandParathyroidectomyPathway interactionsPeripheralPostmenopausePropertyRadialRecruitment ActivityRegulationResearchResearch Project GrantsResearch ProposalsResolutionRoleSignal PathwaySiteSkeletonStem cellsTRANCE proteinWomanX-Ray Computed Tomographybonebone turnoverhuman diseaseindexinginsightinterdisciplinary approachnovel therapeutic interventionskeletalsubstantia spongiosatool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Parathyroid hormone (PTH) is a major regulator of bone and mineral metabolism. However, the manner by which PTH regulates the compartmentalization of trabecular and cortical bone remains unknown. Two diseases of PTH excess and deficiency, primary hyperparathyroidism (PHPT) and hypoparathyroidism (HypoPT), respectively, offer a rich repository of data that suggest roles for PTH not only with regard to circulating biochemical and densitometric indices of mineral metabolism, but perhaps more importantly, for fundamental histomorphometric and structural properties of trabecular and cortical bone. The goal of this research proposal is to apply an interdisciplinary approach to determine how PTH affects compartmentalization and microarchitecture of bone in subjects with PHPT or HypoPT before and after correction of the abnormal PTH state, either by normalization of PTH levels by parathyroidectomy (PHPT) or by administration of PTH (HypoPT). The changes that we expect to see at baseline and after correction of these abnormal PTH states will allow us to attribute, in a manner not previously shown, specific features of the skeleton tha are under the ultimate control of PTH. In addition, I will investigate whether the dual actions of PTH on cortical and trabecular bone can be shifted to a unimodal, osteoanabolic one by blocking its catabolic signaling pathway by denosumab, a specific blocker of receptor activator of nuclear factor kappa B ligand (RANKL). The quantitative tools that will be used in this research project include biochemical markers of bone turnover; bone mineral density by dual-energy x-ray absorptiometry (DXA) and high resolution peripheral quantitative computed tomography (HRpQCT); Finite Element Analysis (FEA); and Individual Trabeculae Segmentation (ITS) analysis.
PUBLIC HEALTH RELEVANCE: Parathyroid hormone (PTH) is a major regulator of bone and mineral metabolism, yet the mechanisms by which PTH regulates compartmentalization and microarchitecture of bone remain unknown. The knowledge obtained in this study should help to better characterize the specific features of the skeleton that are under the ultimate control of PTH. This understanding may lead to the development of new therapeutic interventions.
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Skeletal Regulation of Cortical and Trabecular Bone by Parathyroid Hormone
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批准号:8662770
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项目类别:
-
资助金额:$18.36万
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财政年份:2012
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负责人:Natalie Cusano
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依托单位:
Skeletal Regulation of Cortical and Trabecular Bone by Parathyroid Hormone
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批准号:8496772
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项目类别:
-
资助金额:$18.36万
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财政年份:2012
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负责人:Natalie Cusano
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依托单位:
海外基金