Abstract

BackgroundChronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD) is a significant cause of morbidity among haemodialysis patients and is associated with pathological changes in phosphate, calcium and parathyroid hormone (PTH). In the ACTIVE Dialysis study, extended hours dialysis reduced serum phosphate but did not cause important changes in PTH or serum calcium. This secondary analysis aimed to determine if changes in associated therapies may have influenced these findings and to identify differences between patient subgroups.MethodsThe ACTIVE Dialysis study randomised 200 participants to extended hours haemodialysis (≥24 h/week) or conventional haemodialysis (≤18 h/week) for 12 months. Mean differences between treatment arms in serum phosphate, calcium and PTH; and among key subgroups (high vs. low baseline phosphate/PTH, region, time on dialysis, dialysis setting and frequency) were examined using mixed linear regression.ResultsPhosphate binder use was reduced with extended hours (− 0.83 tablets per day [95% CI -1.61, − 0.04; p = 0.04]), but no differences in type of phosphate binder, use of vitamin D, dose of cinacalcet or dialysate calcium were observed. In adjusted analysis, extended hours were associated with lower phosphate (− 0.219 mmol/L [− 0.314, − 0.124; P < 0.001]), higher calcium (0.046 mmol/L [0.007, 0.086; P = 0.021]) and no change in PTH (0.025 pmol/L [− 0.107, 0.157; P = 0.713]). The reduction in phosphate with extended hours was greater in those with higher baseline PTH and dialysing at home.ConclusionExtended hours haemodialysis independently reduced serum phosphate levels with minimal change in serum calcium and PTH levels. With a few exceptions, these results were consistent across patient subgroups.Trial registrationClinicaltrials.gov NCT00649298. Registered 1 April 2008.

Highlights

  • Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD) is a significant cause of morbidity among haemodialysis patients and is associated with pathological changes in phosphate, calcium and parathyroid hormone (PTH)

  • Reduced renal function is associated with impaired phosphate excretion and diminished conversion of 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D resulting in hypersecretion of parathyroid hormone (PTH) and the osteocyte-derived phosphatonin, fibroblast growth factor-23 (FGF-23)

  • The concentrations of serum phosphate, corrected calcium and intact PTH were similar between groups (Table 1)

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Summary

Introduction

Chronic Kidney Disease - Mineral and Bone Disorder (CKD-MBD) is a significant cause of morbidity among haemodialysis patients and is associated with pathological changes in phosphate, calcium and parathyroid hormone (PTH). Reduced renal function is associated with impaired phosphate excretion and diminished conversion of 25-hydroxyvitamin D to 1,25-dihydroxyvitamin D resulting in hypersecretion of parathyroid hormone (PTH) and the osteocyte-derived phosphatonin, fibroblast growth factor-23 (FGF-23). These changes lead to dysregulation of bone turnover and gastrointestinal absorption of calcium and phosphate, and tissue inhibition of calcification with consequences for bone integrity, mineral metabolism and vascular calcification [6]. The longer term effects of extended dialysis hours achieved predominantly via longer sessions on key markers of CKD-MBD remains less well understood

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