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4A.05: CIRCULATING FGF-23 AS AN INDEPENDENT CORRELATE OF HYPERTENSION AND ATHEROSCLEROSIS IN EARLY STAGES OF CKD.

Title4A.05: CIRCULATING FGF-23 AS AN INDEPENDENT CORRELATE OF HYPERTENSION AND ATHEROSCLEROSIS IN EARLY STAGES OF CKD.
Publication TypeJournal Article
Year of Publication2015
AuthorsDimas, G., Iliadis F., Tegos T., Spiroglou S., Kanellos I., Karamouzis I., Savopoulos C., Hatzitolios A., & Grekas D.
JournalJ Hypertens
Volume33 Suppl 1
Paginatione50
Date Published2015 Jun
ISSN1473-5598
Abstract

OBJECTIVE: Clinical and experimental evidence support a role for fibroblast growth factor (FGF-23) in promoting osteoclastic bone resorption, but the precise molecular mechanisms are not yet fully understood. FGF-23 has been implicated in chronic kidney disease (CKD) and is important in humans for osteogenesis. However, to date the possible role of FGF-23 in secondary hyperparathyroidism (SHP) is still unclear. The aim of this study was to investigate the serum levels of FGF-23 and its potential correlation with blood pressure, atherosclerotic markers and albuminuria in patients with early stages of CKD.DESIGN AND METHOD: CKD patients (n = 50) of stages 1 and 2 with type 2 diabetic nephropathy (DN, n = 25) and chronic glomerulonephritis, (CG, n = 25) were included. As controls, there were two groups, patients with diabetes type 2 without CKD (n = 40) and healthy individuals (n = 40). FGF-23 levels were measured by an ELISA method. Blood pressure (BP) was taken using a manual sphygmomanometer. Intima media thickness (IMT) of carotid arteries as a sub-atherosclerotic marker and presence of atherosclerotic plaque were evaluated by a high resolution ultrasonography. Statistical analysis was performed with the use of a SPSS system.RESULTS: The levels of FGF-23 were significantly higher in patients than in the control groups (0.5 ± 0.1, p < 0.004). IMT was also significantly higher in patients than in the control groups (0.35 ± 0.15, p < 0.001) and albuminuria (300 ± 150, p < 0.0001). There was negative strong correlation between FGF-23 and GFR (r = -0.75, p < 0.005), and positive strong correlation between FGF-23 and BP (0.7, p < 0.0001), between FGF-23 and IMT (r = 0.85, p < 0.0001) and FGF-23 and albuminuria (r = 0.75, p < 0.0001). Further, FGF-23 levels were independent correlates of BP, IMT and albuminuria.CONCLUSIONS: This study suggests that serum levels of FGF-23 were strongly correlated with BP, IMT, atheromatic plaque as well as with albuminuria, attributing a role for FGF-23 in atherosclerosis of CKD patients. FGF-23 might present an independent correlate of atherosclerosis in early stages of CKD.

DOI10.1097/01.hjh.0000467479.89943.a3
Alternate JournalJ. Hypertens.
PubMed ID26102841

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