Mentored Patient Oriented Research in Mineral Metabolism
Mentored Patient Oriented Research in Mineral Metabolism
批准号:
8513987
负责人:
MYLES S WOLF
金额:
$16.15万
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:
2012-08-01 至 2013-09-06
关键词:
African AmericanAngiotensin ReceptorAngiotensin-Converting Enzyme InhibitorsAwardBiological MarkersBiologyBlood PressureCardiacCardiovascular DiseasesCardiovascular systemCaringCategoriesCaucasoid RaceCessation of lifeChronic Kidney FailureChronic Kidney InsufficiencyClinicalClinical DataClinical TrialsCohort StudiesCreatinineDataDatabasesDevelopmentDiagnosticDietDiseaseDisease OutcomeDisease ProgressionEarly treatmentEchocardiographyEnd stage renal failureEpidemicEpidemiologic StudiesEquilibriumEventExhibitsFunctional disorderFutureGoalsHeart failureHormonesHospitalizationHypertensionImageIncidenceIntakeInterventionKidneyKidney DiseasesKnowledgeLeadershipLeft Ventricular HypertrophyLeft Ventricular MassMeasurementMeasuresMentorsMentorshipMetabolismMethodologyMineralsMyocardial InfarctionNational Institute of Diabetes and Digestive and Kidney DiseasesNephrologyNephrosclerosisOutcomeParticipantPatientsPharmaceutical PreparationsPhasePlacebosPopulationProteinuriaPublic HealthRandomizedRelative (related person)ReportingResearchResourcesRiskRisk FactorsSamplingSerumSmokingStagingStimulusStrokeStructureTestingTherapeuticTherapeutic StudiesThickTimeTissuesToxic effectTrainingTranslational ResearchUrsidae FamilyValidationabsorptionadverse outcomeanimal databaseblood pressure regulationcardiovascular disorder riskcareercareer developmentclinical practicecohortdesignfibroblast growth factor 23follow-uphigh riskhuman dataimprovedindexinginorganic phosphatemortalitynew therapeutic targetnovelnovel strategiespatient oriented researchprogramsrandomized trialresearch studyresponsetherapeutic targettool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Disordered phosphate metabolism, marked by elevated levels of the phosphate regulating hormone, fibroblast growth factor 23 (FGF23), is a novel risk factor for cardiovascular disease and mortality in the millions of patients suffering from chronic kidney disease (CKD). High dietary phosphate intake and presence of CKD are major stimuli for FGF23 secretion. In these settings, a progressive increase in FGF23 levels is an appropriate adaptation to maintain normal phosphate balance. However, studies from our team and others demonstrate that elevated FGF23 is a powerful, independent risk factor for more rapid CKD progression and mortality. As a potential mechanism of increased mortality, we recently demonstrated that elevated FGF23 contributes causally to the frequent development of left ventricular hypertrophy in CKD patients. These data suggest that elevated FGF23 may represent not only a potentially powerful risk-stratifying biomarker but also a novel therapeutic target to improve outcomes in CKD. The PI's overarching scientific career goal is to demonstrate by randomized trial that early delivery of interventions based on FGF23 testing, or specifically targeting elevated FGF23 levels, will slow progression of CKD, reduce cardiovascular disease events and improve survival. Justifying a large-scale clinical trial requires further knowledge of FGF23 biology, the mechanisms of its toxicity, validation of its impact on outcomes in epidemiological studies that analyze FGF23 repeatedly over time, and detailed patient-oriented research studies to characterize the efficacy of candidate interventions on reducing FGF23 levels. In Aim 1 of this K24 application, we will perform a secondary analysis of the African American Study of Kidney Disease and Hypertension. We will test the association between FGF23 and cardiac structure and function as determined by echocardiography~ we will examine single and repeated measures of FGF23 as a novel risk factor for adverse renal and cardiovascular outcomes~ and we will use emerging tools to quantify the utility of FGF23 testing as a risk-stratifying biomarker in CKD. In Aim 2, we will tes the effect of dietary phosphate restriction and phosphate binders alone and in combination as candidate interventions to lower FGF23 levels in CKD stage 3-4 patients. These studies will be excellent training vehicles for the PI's trainees and will be further enhanced by an ongoing parallel program in translational research that the PI will continue to cultivate as one of his career development activities during this award. Other career development activities include formal coursework in leadership and the implementation of a new educational initiative in the Division of Nephrology to attract additional fellows to patient-oriented research. The K24 will provide the PI with critically important protected time and dedicated resources to expand his mentorship activities, grow his own research program and further advance his career as a leader in patient-oriented research in nephrology.
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科研奖励(0)
会议论文
Tissue-Specific Regulation and Effects of CYP24A1
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批准号:10580931
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项目类别:
-
资助金额:$54.75万
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财政年份:2023
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负责人:MYLES S WOLF
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依托单位:
HiLo
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批准号:10468020
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项目类别:
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资助金额:$129.83万
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财政年份:2019
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负责人:MYLES S WOLF
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依托单位:
HiLo
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批准号:10229378
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项目类别:
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资助金额:$132.8万
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财政年份:2019
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负责人:MYLES S WOLF
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依托单位:
HiLo
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批准号:9753568
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项目类别:
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资助金额:$144.42万
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财政年份:2019
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负责人:MYLES S WOLF
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依托单位:
Pilot Studies Targeting Mineral Metabolism in CKD
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批准号:8829382
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项目类别:
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资助金额:$34.38万
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财政年份:2014
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负责人:MYLES S WOLF
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依托单位:
FGF23 and mineral metabolism in Acute Kidney Injury
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批准号:8771298
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项目类别:
-
资助金额:$26.06万
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财政年份:2014
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负责人:MYLES S WOLF
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依托单位:
FGF23 and Cardiovascular Disease in CKD
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批准号:8702151
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项目类别:
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资助金额:$59.21万
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财政年份:2013
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负责人:MYLES S WOLF
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依托单位:
FGF23 and Cardiovascular Disease in CKD
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批准号:8906843
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项目类别:
-
资助金额:$54.46万
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财政年份:2013
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负责人:MYLES S WOLF
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依托单位:
FGF23 and Cardiovascular Disease in CKD
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批准号:9462546
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项目类别:
-
资助金额:$38.48万
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财政年份:2013
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负责人:MYLES S WOLF
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依托单位:
Role of FGF23 in Mineral Metabolism Across the Spectrum of Chronic Kidney Disease
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批准号:8728815
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项目类别:
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资助金额:$19.86万
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财政年份:2013
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负责人:MYLES S WOLF
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依托单位:
Role of FGF23 in Mineral Metabolism Across the Spectrum of Chronic Kidney Disease
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批准号:8841986
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项目类别:
-
资助金额:$21.22万
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财政年份:2013
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负责人:MYLES S WOLF
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依托单位:
Pilot Studies Targeting Mineral Metabolism in Chronic Kidney Disease
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批准号:8733682
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项目类别:
-
资助金额:$34.38万
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财政年份:2013
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负责人:MYLES S WOLF
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依托单位:
FGF23 and Cardiovascular Disease in CKD
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批准号:8822717
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项目类别:
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资助金额:$56.43万
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财政年份:2013
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负责人:MYLES S WOLF
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依托单位:
Mentored Patient Oriented Research in Mineral Metabolism
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批准号:8930962
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项目类别:
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资助金额:$16.04万
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财政年份:2012
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负责人:MYLES S WOLF
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依托单位:
Mentored Patient Oriented Research in Mineral Metabolism
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批准号:8828957
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项目类别:
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资助金额:$16.15万
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财政年份:2012
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负责人:MYLES S WOLF
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依托单位:
Mentored Patient Oriented Research in Mineral Metabolism
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批准号:9385039
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项目类别:
-
资助金额:$15.65万
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财政年份:2012
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负责人:MYLES S WOLF
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依托单位:
Mentored Patient Oriented Research in Mineral Metabolism
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批准号:8384451
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项目类别:
-
资助金额:$16.35万
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财政年份:2012
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负责人:MYLES S WOLF
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依托单位:
FGF23 and Cardiovascular Disease in CKD
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批准号:8245248
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项目类别:
-
资助金额:$6.29万
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财政年份:2008
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负责人:MYLES S WOLF
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依托单位:
FGF23 and Cardiovascular Disease in CKD
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批准号:8372439
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项目类别:
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资助金额:$56.1万
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财政年份:2008
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负责人:MYLES S WOLF
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依托单位:
FGF23 and Cardiovascular Disease in CKD
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批准号:7903995
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项目类别:
-
资助金额:$32.43万
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财政年份:2008
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负责人:MYLES S WOLF
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依托单位:
海外基金