An elevated level of the phosphate regulating hormone fibroblast growth factor 23 (FGF23) is an independent risk factor for cardiovascular disease (CVD) and mortality across the spectrum of chronic kidney disease (CKD). Elevated FGF23 contributes directly to the pathogenesis of left ventricular hypertrophy, suggesting one potential mechanism for the high risk of CVD and death that is attributable to elevated FGF23. Preliminary data that demonstrate that elevated FGF23 is a powerful risk factor for congestive heart failure confirms the clinical relevance of FGF23-mediated LVH. Thus, data generated during the first 4 years of support under this award established elevated FGF23 as a novel biomarker and mechanism of adverse outcomes in CKD, and thus, novel therapeutic target. Additional work from our group was also the first to suggest a survival benefit of active vitamin D therapy in ESRD. However, active vitamin D raises FGF23, which might be expected to accelerate mortality. Reconciling this potential paradox is a central theme of this application. Based on preliminary data, we hypothesize that vitamin D may attenuate cardiac toxicity of FGF23 despite raising FGF23 levels, and that CKD patients'variable FGF23 response to active vitamin D, ranging from minimal to large increases, modifies their CVD risk and survival experience.
In Aim 1, we will test the hypothesis that the magnitude of change in FGF23 in response to active vitamin D therapy modulates risk of mortality in a large prospective cohort of incident hemodialysis patients.
In Aim 2, we will analyze FGF23 in a secondary analysis of a recently completed randomized trial of active vitamin D versus placebo in CKD stage 3-4 patients to test the hypothesis that baseline and follow-up FGF23 levels modify the cardiac structural and functional response to active vitamin D therapy. Previous studies suggest that non-calcium based phosphate binders lower FGF23, but there have been no placebo-controlled studies >2 weeks duration, and no studies examined the impact of FGF23 reduction on intermediate measures of CVD risk in CKD stage 3-4 patients with normal serum phosphate. Furthermore, no studies investigated the utility of combining phosphate binders with active vitamin D to potentially maximize their dual benefits on mineral metabolism and CVD.
In Aim 3, we will conduct a one- year, placebo-controlled, 2 x 2 factorial, randomized study of CKD stage 3-4 patients to test the effects of active vitamin D and phosphate binders alone and in combination on FGF23, other mineral metabolites, and a comprehensive set of intermediate measures of CVD risk. Extensive preliminary data support our hypotheses, and our research team has the requisite expertise in FGF23, vitamin D, observational cohorts, and randomized studies with repeated measures to successfully complete these Aims. Renewed support will enable us to generate data that are critical for the rational design of larger trials in the futureand thereby support our long- term goal of translating FGF23 research into meaningful improvements in the management of CKD.
A high circulating level of the phosphate regulating hormone fibroblast growth factor 23 (FGF23) is a strong risk factor for kidney failure, cardiovascular disease and death among patients with chronic kidney disease. Since FGF23 levels increase early in the course of chronic kidney disease, testing for FGF23 could be used to identify candidates for earlier treatment of abnormal phosphate metabolism than is the current standard practice. This application will investigate strategies to lower FGF23 levels and the effect these approaches have on the cardiovascular system and survival. Since chronic kidney disease affects 23 million adults in the US, identifying novel therapeutic strategies to prevent its complications could have a major public health impact.
|Souma, Nao; Isakova, Tamara; Lipiszko, David et al. (2016) Fibroblast Growth Factor 23 and Cause-Specific Mortality in the General Population: The Northern Manhattan Study. J Clin Endocrinol Metab 101:3779-3786|
|Singh, Saurav; Grabner, Alexander; Yanucil, Christopher et al. (2016) Fibroblast growth factor 23 directly targets hepatocytes to promote inflammation in chronic kidney disease. Kidney Int 90:985-996|
|David, Valentin; Wolf, Myles (2016) Pruning the ricket thicket. J Clin Invest 126:473-6|
|GutiÃ©rrez, Orlando M; Parsa, Afshin; Isakova, Tamara et al. (2016) Genetic African Ancestry and Markers of Mineral Metabolism in CKD. Clin J Am Soc Nephrol 11:653-62|
|David, Valentin; Martin, Aline; Isakova, Tamara et al. (2016) Inflammation and functional iron deficiency regulate fibroblast growth factor 23 production. Kidney Int 89:135-46|
|Faul, Christian; Wolf, Myles (2015) Hunt for the culprit of cardiovascular injury in kidney disease. Cardiovasc Res 108:209-11|
|Scialla, Julia J; Wolf, Myles (2015) When there will never be a randomized controlled trial. Kidney Int 88:220-2|
|Eckberg, Karl; Kramer, Holly; Wolf, Myles et al. (2015) Impact of westernization on fibroblast growth factor 23 levels among individuals of African ancestry. Nephrol Dial Transplant 30:630-5|
|Wolf, Myles; Mehta, Rupal (2015) Fibroblast Growth Factor-23 Fans the Flames of Heart and Kidney Failure. JACC Heart Fail 3:840-2|
|Grabner, Alexander; Amaral, Ansel P; Schramm, Karla et al. (2015) Activation of Cardiac Fibroblast Growth Factor Receptor 4 Causes Left Ventricular Hypertrophy. Cell Metab 22:1020-32|
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