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KMID : 1100120180250030153
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2018 Volume.25 No. 3 p.153 ~ p.159
Linkage of Fibroblast Growth Factor 23 and Phosphate in Serum: Phosphate and Fibroblast Growth Factor 23 Reduction by Increasing Dose of Sevelamer
Ghorbanihaghjo Amir

Argani Hassan
Golmohamadi Zahra
Rashtchizadeh Nadereh
Abbasi Mehran Mesgari
Bargahi Nasrin
Vatankhah Amir Mansour
Sanajou Davoud
Abstract
Background: High serum phosphate and fibroblast growth factor-23 (FGF-23) levels are well-recognized independent risk factors of mortality and morbidity in patients with chronic kidney diseases (CKDs). Sevelamer, as a phosphate chelating agent, reduces serum phosphate and FGF-23 levels produced by bone osteocytes. This study aimed to determine the best dose at which sevelamer could successfully reduce serum phosphate and FGF-23 levels in rat models of adenine-induced CKD.

Methods: CKD was induced using adenine. Healthy and CKD-induced rats were divided into 6 groups as follows: healthy controls; CKD controls; rats treated with 1%, 2%, and 3% sevelamer for CKDs; and healthy rats administered 3% sevelamer. Biochemical factors and serum FGF-23 levels were measured using spectrophotometry and enzyme-linked immunosorbent assay methods.

Results: Serum phosphate levels were best decreased in rats receiving 3% sevelamer in their diet (5.91¡¾1.48 mg/dL vs. 8.09¡¾1.70 mg/dL, P<0.05) compared with the CKD control rats. A dose-dependent decrease in serum FGF-23 levels was observed, and the most significant results were obtained in rats receiving 3% sevelamer compared with the CKD control rats (142.60¡¾83.95 pg/mL vs. 297.15¡¾131.10 pg/mL, P<0.01).

Conclusions: Higher sevelamer doses significantly reduced serum phosphate and FGF-23 levels in adenine-induced CKD rats.
KEYWORD
Chronic, Phosphates, Renal insufficiency, Sevelamer
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