Abstract

Background: Arterial calcification is a predictive marker in patient on hemodialysis (HD), but the relationship between arterial calcification and calciprotein particles (CPPs) is unclear. Methods: We examined the effects of ferric citrate hydrate (JTT-751) on CPP level and evaluated changes in aortic arch calcification (AoAC) grade in patients on maintenance HD (MHD). In total, 70 MHD patients were enrolled in the study and followed for 24 months. We measured serum CPP levels and fibroblast growth factor 23 (FGF 23) among propensity score-matched MHD patients. One group (n = 35) was treated with CaCO3 and the other (n = 35) was treated with ferric citrate hydrate (JTT-751). AoAC was assessed on chest-X rays. Eligible patients continued the same treatment. Results: All 70 patients completed the study. Serum CPP levels reduced in the JTT-751 group, but were not significantly different in the CaCO3 group. Among patients whose baseline AoAC score (AoACS) was ≤ 4 (median), median AoACS increased from 0 (0 - 3) to 3 (2 - 4) (p 3 group, median AoACS increased from 2 (0 - 2) to 3 (0 - 4) (p < 0.05) and Δ% AoACS was 1 (0% - 3%). Conclusion: These results indicate that the administration of JTT-751 decreased serum CPP levels but did not inhibit AoAC progression in patients on MHD.

Highlights

  • High serum phosphate (P) level is a frequent manifestation in advanced chronic kidney disease (CKD) and an important factor for CKD-mineral bone disorder (CKD-MBD) [1]

  • We examined the effects of ferric citrate hydrate (JTT-751) on calciprotein particles (CPPs) level and evaluated changes in aortic arch calcification (AoAC) grade in patients on maintenance HD (MHD)

  • This evaluation of AoAC progression with JTT-751 compared with CaCO3 in patients on MHD is the first to our knowledge

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Summary

Introduction

High serum phosphate (P) level is a frequent manifestation in advanced chronic kidney disease (CKD) and an important factor for CKD-mineral bone disorder (CKD-MBD) [1]. CPP levels correlate significantly with serum levels of P and fibroblast growth factor 23 (FGF23), but not with Ca levels, and can increase in CKD patients with hyperphosphatemia or hypocalcemia [9]. Methods: We examined the effects of ferric citrate hydrate (JTT-751) on CPP level and evaluated changes in aortic arch calcification (AoAC) grade in patients on maintenance HD (MHD). We measured serum CPP levels and fibroblast growth factor 23 (FGF 23) among propensity score-matched MHD patients. Serum CPP levels reduced in the JTT-751 group, but were not significantly different in the CaCO3 group. Conclusion: These results indicate that the administration of JTT-751 decreased serum CPP levels but did not inhibit AoAC progression in patients on MHD

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