Your browser doesn't support javascript.
loading
Long-Term Effects of Sevelamer on Vascular Calcification, Arterial Stiffness, and Calcification Propensity in Patients Receiving Peritoneal Dialysis: The Randomized Pilot SERENE (Sevelamer on Vascular Calcification, Arterial Stiffness) Trial.
Wang, Angela Yee-Moon; Pasch, Andreas; Wong, Chun-Kwok; Chu, Ida Miu-Ting; Tang, Tak-Ka; Chu, Jessie; Cheuk-Ying Fong, Charmaine; Yau, Yat-Yin; Lo, Wai-Kei.
Afiliação
  • Wang AY; Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China.
  • Pasch A; Institute for Physiology and Pathophysiology, Johannes Kepler University Linz, Linz, Austria.
  • Wong CK; Practice for Internal Medicine and Nephrology at Hirschengraben, Bern, Switzerland.
  • Chu IM; Calciscon AG, Biel, Switzerland.
  • Tang TK; Department of Nephrology, Lindenhofspital Bern and Nierenpraxis Bern, Bern, Switzerland Calciscon AG, Nidau, Switzerland.
  • Chu J; Department of Chemical Pathology, Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong SAR, China.
  • Cheuk-Ying Fong C; Department of Chemical Pathology, Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong SAR, China.
  • Yau YY; Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China.
  • Lo WK; Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong SAR, China.
Kidney Med ; 4(2): 100384, 2022 Feb.
Article em En | MEDLINE | ID: mdl-35243302
ABSTRACT
RATIONALE &

OBJECTIVE:

There is a concern regarding increased risk of vascular calcification with the use of calcium-based phosphorus binders. This study aimed to compare the effects of sevelamer used as a second-line, low-dose therapy with calcium-based phosphorus binders with those of sevelamer used as a first-line, high-dose therapy on coronary artery and heart valve calcification, aortic pulse wave velocity (PWV), and calcification propensity over 2 years in patients with hyperphosphatemia receiving peritoneal dialysis (PD). STUDY

DESIGN:

A 2-year-long prospective, multicenter, open-label, randomized pilot study. SETTING &

PARTICIPANTS:

Prevalent patients with hyperphosphatemia receiving PD from 2 university-affiliated hospitals in Hong Kong.

INTERVENTIONS:

The patients were randomized to receive sevelamer either as a first-line therapy at a high dose of 800 mg thrice daily (can titrate up to 1,200 mg thrice daily as required) or a second-line therapy at a low dose of 400 mg thrice daily with calcium carbonate to achieve a serum phosphorus target of ≤5.5 mg/dL.

OUTCOMES:

The primary endpoints were changes in coronary artery calcium score and aortic PWV over 104 weeks. The secondary endpoints were changes in heart valve calcium scores, calcification propensity measure, and biochemical parameters of chronic kidney disease-mineral bone disease over 104 weeks.

RESULTS:

Among 60 prevalent patients receiving PD, with a mean age of 53 ± 10 years and with 57% men, changes in the coronary artery calcium score (median [interquartile range], 225 [79-525] vs 223 [56-1,212], respectively; P = 0.21), aortic PWV (mean ± standard error, 0.3 ± 0.1 vs 0.8 ± 0.2 m/s, respectively; P = 0.31), heart valve calcium score, maturation or transformation time, serum calcium levels, and phosphorus levels over 104 weeks were similar for the second-line, low-dose and first-line, high-dose sevelamer groups. Alkaline phosphatase and intact parathyroid hormone levels increased and low-density lipoprotein cholesterol decreased in both the groups, with no significant between-group differences.

LIMITATIONS:

The sample size was small, and the dropout rates were relatively high.

CONCLUSIONS:

Low-dose sevelamer used as a second-line therapy for hyperphosphatemia in combination with a calcium-based phosphorus binder had similar effects on vascular calcification, valvular calcification, and arterial stiffness compared with high-dose sevelamer used as a first-line therapy. This approach may be considered in resource-constrained countries to minimize calcium loading.

FUNDING:

The study was supported by a competitive grant from SK Yee Medical Foundation. T50 assays and other biochemical assays were funded by a research grant from Sanofi Renal Corporation. TRIAL REGISTRATION NCT00745589.
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article