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Vitamin D Deficiency in Glomerular Disease

Vitamin D Deficiency in Glomerular Disease
肾小球疾病中维生素 D 缺乏
批准号:
8442549
负责人:
Michelle Denburg
金额:
$17.11万
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:
2012-09-15 至 2017-07-31
关键词:
1,25 (OH) vitamin D25-hydroxyvitamin DAddressAdultAdverse effectsAgeAlbuminsAnimalsArchivesBinding ProteinsBiometryBiopsyCalciumCardiovascular DiseasesCardiovascular systemCatabolismChemotactic FactorsChildChildhoodCholecalciferolChronic Kidney FailureClinical ImmunologyClinical TrialsCross-Sectional StudiesDataDevelopmentDevelopment PlansDialysis procedureDiseaseDisease ProgressionEndocytosisEnzymesEpidemiologyErgocalciferolsExcretory functionFocal Segmental GlomerulosclerosisFunctional disorderFundingGlomerular Filtration RateGoalsGuidelinesHealthHistopathologyHumanHypercalcemiaImmune responseImmunityImmunologyIncidenceInfectionInflammationInjuryInsulin ResistanceInterventionKidneyKidney DiseasesLDL-Receptor Related Protein 2LeadLinkMeasuresMediatingMentorshipMetabolicMetabolismMineralsMixed Function OxygenasesMolecular WeightNatural ImmunityNephrologyNephrotic SyndromeOutcomeParticipantPathway interactionsPatientsPhosphorusPilot ProjectsPopulationProtein BindingProteinsProteinuriaRegimenRenal glomerular diseaseReportingResearchResearch InstituteResearch PersonnelResearch TrainingResourcesRisk FactorsSafetySerumSeveritiesSpecimenSupplementationTherapeuticToxic effectTrainingTraining ProgramsTranslational ResearchTubular formationUnited States National Institutes of HealthVitamin DVitamin D DeficiencyVitamin D-Binding ProteinWorkantimicrobialcareer developmentcathelicidinclinical epidemiologydesignfibroblast growth factor 23high riskhypercalciuriaimmune functionimprovedinsightintrinsic factor-cobalamin receptormRNA Expressionmacrophagemodifiable riskmonocytenovelpatient populationpodocytepreventprogramsprospectiveprotein complexrepositoryresponseskeletaluptakeurinaryyoung adult

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中文摘要
翻译
应聘者描述(申请人提供):应聘者为儿科肾病初级研究员,受过临床流行病学方面的高级培训。她的研究重点是维生素D的骨外作用,以及在肾小球疾病合并肾病范围蛋白尿患者中管理维生素D缺乏的独特挑战。维生素D缺乏可能是这些患者肾脏疾病进展和并发症的一个重要的可改变的危险因素。许多小规模研究证明,肾病患者的总25-羟基维生素D[25(OH)D]水平非常低,但其潜在的病理生理机制却鲜为人知。此外,必须确定在这个庞大的患者群体中补充的安全性和有效性,以防止潜在的毒性和治疗不足。候选人的初步工作表明,肾小球疾病,特别是局灶性节段性肾小球硬化(FSGS),是慢性肾脏疾病儿童总25(OH)D和游离25(OH)D水平和维生素D结合蛋白(DBP)水平低的独立危险因素。这些发现表明25(OH)D-DBP复合体的肾小管重吸收受损和/或维生素D分解代谢增加。拟议的项目包括:(1)对NIH资助的肾病综合征研究网络(NEPOUNT)的450名参与者进行辅助横断面研究;(2)对35名患有FSGS的儿童和年轻人进行补充胆钙化醇的试点研究。利用海王星独特的标准化组织病理学数据库,这项工作将首次确定肾小管间质损伤与维生素D代谢物之间的联系,并描绘成纤维细胞生长因子23促进的分解代谢对这些患者维生素D水平的影响。这项补充研究将探讨在蛋白尿性FSGS患者中补充钙化醇的安全性和有效性,并使用先天免疫和肾内炎症的新翻译指标来评估补充的反应。这项工作的发现将对后续维生素D试验的设计和实施以及补充指南的制定至关重要。候选人的全面职业发展计划包括临床试验和免疫学的授课培训,以及流行病学、生物统计学、肾脏病和免疫学领导人的指导。她将利用包括CHOP研究所和CTSA、临床流行病学和生物统计中心以及海王星在内的杰出资源。她的短期目标是:(1)将75%的精力投入到这项研究和培训计划中;(2)随后争取国家卫生研究院的资金,以支持维生素D补充剂的试验及其对肾小球疾病患者免疫功能和感染并发症的影响;(3)扩大海王星研究,将基线维生素D水平和矿物质代谢指标与心血管疾病、感染和肾脏疾病进展联系起来。她的长期目标是领导一项由NIH资助的针对患有肾小球疾病的儿童和成人的转化研究计划,重点是在这一高危人群中减少并发症和疾病进展的干预措施。 公共卫生相关性:维生素D缺乏与各种不利的健康后果有关。肾病患者的维生素D水平非常低,其潜在机制尚不清楚。此外,在这些患者中安全有效地补充维生素D的方法还没有建立。从这项研究中获得的见解对于指导维生素D治疗的后续试验是必要的,以改善结果,并为患有肾病综合征的儿童和成人制定独特的补充指南。
英文摘要
DESCRIPTION (provided by applicant): The candidate is a junior investigator in pediatric nephrology with advanced training in clinical epidemiology. Her research is focused on the extra-skeletal actions of vitamin D and the unique challenges of managing vitamin D deficiency in patients with glomerular diseases complicated by nephrotic-range proteinuria. Vitamin D deficiency may be an important modifiable risk factor for renal disease progression and complications in these patients. Many small studies documented very low total 25-hydroxyvitamin D [25(OH)D] levels in nephrotic patients, but the underlying pathophysiology is poorly understood. Further, the safety and efficacy of supplementation in this sizeable patient population must be determined in order to prevent both potential toxicity and under-treatment. The candidate's preliminary work demonstrated that glomerular disease, particularly focal segmental glomerulosclerosis (FSGS), was an independent risk factor for low total and free 25(OH) D levels and vitamin D-binding protein (DBP) in children with chronic kidney disease. These findings implicate impaired tubular reabsorption of 25(OH) D-DBP complexes and/or increased vitamin D catabolism. The proposed project comprises: (1) an ancillary cross-sectional study of 450 participants in the NIH-funded Nephrotic Syndrome Study Network (NEPTUNE) and (2) a pilot study of cholecalciferol supplementation in 35 children and young adults with FSGS. Leveraging NEPTUNE's unique repository of standardized histopathology data, this work will be the first to determine the association between tubulointerstitial injury an vitamin D metabolites and to delineate the impact of fibroblast growth factor 23-promoted catabolism on vitamin D levels in these patients. The supplementation study will address the safety and efficacy of calciferol supplementation in proteinuric FSGS patients and use novel translational measures of innate immunity and intra-renal inflammation to assess the response to supplementation. The findings of this work will be critical to the design and conduct of subsequent vitamin D trials, and to the development of supplementation guidelines. The candidate's comprehensive career development plan includes didactic training in clinical trials and immunology, and mentorship by leaders in epidemiology, biostatistics, nephrology and immunology. She will draw on outstanding resources including the CHOP Research Institute and CTSA, the Center for Clinical Epidemiology and Biostatistics, and NEPTUNE. Her short-term goals are to: (1) dedicate 75% effort to this research and training program; (2) subsequently compete for NIH funds to support a trial of vitamin D supplementation and its impact on immune function and infectious complications in patients with glomerular diseases; and (3) expand the NEPTUNE study to relate baseline vitamin D levels and measures of mineral metabolism to cardiovascular disease, infections and renal disease progression. Her long-term goal is to lead an NIH-funded translational research program in children and adults with glomerular disease, with an emphasis on interventions to reduce complications and disease progression in this high-risk population. PUBLIC HEALTH RELEVANCE: Vitamin D deficiency has been linked to a variety of adverse health outcomes. Nephrotic patients have very low vitamin D levels, and the underlying mechanisms are not known. Furthermore, approaches to safely and effectively supplement vitamin D in these patients have not been established. The insights gained from this study are necessary to inform subsequent trials of vitamin D therapy to improve outcomes and develop unique supplementation guidelines for children and adults with diseases complicated by nephrotic syndrome.
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