A prospective study of the influence of the skeleton on calcium mass transfer during hemodialysis

PLoS One. 2018 Jul 30;13(7):e0198946. doi: 10.1371/journal.pone.0198946. eCollection 2018.

Abstract

Background: Calcium gradient, the difference between serum calcium and dialysate calcium d[Ca], is the main contributor factor influencing calcium transfer during hemodialysis. The impact, however, of bone turnover, on calcium mass transfer during hemodialysis is still uncertain.

Methods: This prospective cross-sectional study included 10 patients on hemodialysis for a 57.6±16.8 months, with severe hyperparathyroidism. Patients were submitted to 3 hemodialysis sessions using d[Ca] of 1.25, 1.5 and 1.75 mmol/l in three situations: pre-parathyroidectomy (pre-PTX), during hungry bone (early post-PTX), and after stabilization of clinical status (late post-PTX). Biochemical analysis and calcium mass transfer were evaluated and serum bone-related proteins were quantified.

Results: Calcium mass transfer varied widely among patients in each study phase with a median of -89.5, -76.8 and -3 mmol using d[Ca] 1.25 mmol/L, -106, -26.8 and 29.7 mmol using d[Ca] 1.50 mmol/L, and 12.8, -14.5 and 38 mmol using d[Ca] 1.75 mmol/L during pre-PTX, early post-PTX and late post-PTX, respectively, which was significantly different among d[Ca] (p = 0.0001) and among phases (p = 0.040). Ca gradient and delta of Ca also differed among d[Ca] and phases (p<0.05 for all comparisons), whether ultrafiltration was similar. Serum Osteocalcin decreased significantly in late post-PTX, whereas Sclerostin increased earlier, in early post-PTX.

Conclusions: The skeleton plays a key role in Ca mass transfer during dialysis, either by determining pre-dialysis serum Ca or by controlling the exchangeable Ca pool. Knowing that could help us to decide which d[Ca] should be chosen in a given patient.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Adult
  • Bone Morphogenetic Proteins / blood
  • Bone Morphogenetic Proteins / genetics
  • Bone and Bones / metabolism*
  • Bone and Bones / pathology
  • Calcium / metabolism*
  • Calcium Signaling
  • Cross-Sectional Studies
  • Female
  • Gene Expression Regulation
  • Genetic Markers / genetics
  • Humans
  • Hyperparathyroidism, Secondary / blood*
  • Hyperparathyroidism, Secondary / genetics
  • Hyperparathyroidism, Secondary / pathology
  • Hyperparathyroidism, Secondary / surgery
  • Ion Transport
  • Male
  • Middle Aged
  • Osteocalcin / blood
  • Osteocalcin / genetics
  • Parathyroid Hormone / blood
  • Parathyroid Hormone / genetics
  • Parathyroidectomy*
  • Prospective Studies
  • Renal Dialysis / methods*
  • Renal Insufficiency, Chronic / blood*
  • Renal Insufficiency, Chronic / genetics
  • Renal Insufficiency, Chronic / pathology
  • Renal Insufficiency, Chronic / therapy

Substances

  • Adaptor Proteins, Signal Transducing
  • BGLAP protein, human
  • Bone Morphogenetic Proteins
  • Genetic Markers
  • Parathyroid Hormone
  • SOST protein, human
  • Osteocalcin
  • Calcium

Grants and funding

Research in the laboratory of RMAM is supported by CNPQ, Conselho Nacional de Desenvolvimento Científico e Tecnológico (grants 304249/2013-0 and 303899/2016-6) and Fundação de Amparo à Pesquisa do Estado de São Paulo (grant 2010/20549-9). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.