Citric-acid dialysate improves the calcification propensity of hemodialysis patients: A multicenter prospective randomized cross-over trial.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2019
Historique:
received: 31 03 2019
accepted: 12 11 2019
entrez: 6 12 2019
pubmed: 6 12 2019
medline: 25 3 2020
Statut: epublish

Résumé

The concentration of dialysate calcium (dCa) has been suggested to affect vascular calcification, but evidence is scarce. Calcification propensity reflects the intrinsic capacity of serum to prevent calcium and phosphate to precipitate. The use of citric-acid dialysate may have a beneficial effect on the calcification propensity due to the chelating effect on calcium and magnesium. The aim of this study was to compare the intradialytic and short-term effects of haemodialysis with either standard acetic-acid dialysate with dCa1.50 (A1.5) or dCa1.25 (A1.25), as well as citric-acid dialysate with dCa1.50 (C1.5) in bicarbonate dialysis on the calcification propensity of serum. Chronic stable hemodialysis patients were included. This multicenter randomized cross-over study consisted out of a baseline week (A1.5), followed by the randomized sequence of A1.25 or C1.5 for one week after which the alternate treatment was provided after a washout week with A1.5. Calcification propensity of serum was assessed by time-resolved nephelometry where the T50 reflects the transition time between formation of primary and secondary calciprotein particles. Eighteen patients (median age 70 years) completed the study. Intradialytic change in T50 was increased with C1.5 (121 [90-152]min) compared to A1.25 (83 [43-108]min, p<0.001) and A1.5 (66 [18-102]min, p<0.001). During the treatment week, predialysis T50 increased significantly from the first to the third session with C1.5 (271 [234-291] to 280 [262-339]min, p = 0.002) and with A1.25 (274 [213-308] to 307 [256-337]min, p<0.001), but not with A1.5 (284 [235-346] to 300 [247-335]min, p = 0.33). Calcification propensity, as measured by the change in T50, improved significantly during treatment in C1.5 compared to A1.25 and A1.5. Long-term studies are needed to investigate the effects of different dialysate compositions concentrations on vascular calcification and bone mineral disorders.

Identifiants

pubmed: 31805104
doi: 10.1371/journal.pone.0225824
pii: PONE-D-19-05164
pmc: PMC6894765
doi:

Substances chimiques

Citric Acid 2968PHW8QP
Calcium SY7Q814VUP

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0225824

Déclaration de conflit d'intérêts

Bernard Canaud and Adelheid Gauly are employed by Fresenius MC and may hold shares in this company. FS and JK received a grant of Fresenius Medical Care. With this they have set up this trial with BC, MD and KM. Andreas Pasch, Isabelle Gsponer and Matthias Bachtler are employed by Calciscon AG. Andreas Pasch holds shares in this company. Calciscon AG holds the following patent for the T50-Test [A Method For Determining The Propensity For Calcification (PCT/EP2012/071971)] and markets the T50- Test. There are no other patents, products in development or marketed products to declare. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Karlien J Ter Meulen (KJ)

Department of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Department of Internal Medicine, Division of Nephrology, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.

Marijke J E Dekker (MJE)

Department of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.
Department of Internal Medicine, Division of Nephrology, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.

Andreas Pasch (A)

Calciscon AG, Nidau, Switzerland.

Natascha J H Broers (NJH)

Department of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.

Frank M van der Sande (FM)

Department of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.

Jeroen B van der Net (JB)

Department of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.

Constantijn J A M Konings (CJAM)

Department of Internal Medicine, Division of Nephrology, Catharina Hospital Eindhoven, Eindhoven, the Netherlands.

Isabelle M Gsponer (IM)

Calciscon AG, Nidau, Switzerland.

Matthias D N Bachtler (MDN)

Calciscon AG, Nidau, Switzerland.

Adelheid Gauly (A)

Fresenius Medical Care, Bad Homburg, Germany.

Bernard Canaud (B)

Fresenius Medical Care, Bad Homburg, Germany.

Jeroen P Kooman (JP)

Department of Internal Medicine, Division of Nephrology, Maastricht University Medical Center+, Maastricht, the Netherlands.

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