Conventional versus ultrapure dialysate for lowering serum lipoprotein(a) levels in patients on long-term hemodialysis: a randomized trial

Int J Artif Organs. 2010 May;33(5):290-6.

Abstract

Purpose: In patients on long-term hemodialysis, high lipoprotein(a) [Lp(a)] levels are difficult to lower with medications, although they remain a risk factor for cardiovascular disease. We investigated whether ultrapure dialysate (UPD) could lower Lp(a).

Methods: We randomly assigned patients stabilized on long-term dialysis to either a low-flux synthetic polysulphone membrane (the UPD group; n=14) or to a conventional dialysate (the CD group; n=13). Blood samples were collected 1 week before dialysis and 1 week, 1 month, 6 months and 12 months after dialysis; Lp(a) was measured by the immunoturbidimetry method. Hemoglobin, interleukin-6, hypersensitive C-reactive protein, beta(2) microglobulin and albumin were also measured. The erythropoietin dosage, Kt/V, and normalized protein catabolic rate were recorded monthly.

Results: At 12 months, mean (SD) serum levels of Lp(a) in the CD patients increased from 143.46 (125.11) to 283.89 (145.81) mg/L (p<0.01), whereas levels in the UPD group remained unchanged: 131.38 (201.45) to 120.90 (122.11) mg/L. Endotoxin levels in the 10 CD patients who completed the study ranged from 0.116 to 0.349 EU/mL and were undetectable in the 11 UPD patients who completed the study. The cultures were less than 200 CFU/mL in CD patients and negative all the time for all UPD patients. Changes in Lp(a) from baseline values were lower in the UPD group than in the CD group (p<0.05). However, changes in other variables did not differ between groups.

Conclusions: Ultrapure dialysate can prevent the rise of Lp(a), potentially decreasing the risk of cardiovascular disease in hemodialysis patients.

Publication types

  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Biomarkers / blood
  • C-Reactive Protein / metabolism
  • Cardiovascular Diseases / blood
  • Cardiovascular Diseases / etiology
  • Cardiovascular Diseases / prevention & control
  • Down-Regulation
  • Endotoxins / blood
  • Erythropoietin / therapeutic use
  • Female
  • Hematinics / therapeutic use
  • Hemodialysis Solutions / therapeutic use*
  • Hemoglobins / metabolism
  • Humans
  • Inflammation Mediators / blood
  • Interleukin-6 / blood
  • Kidney Failure, Chronic / blood
  • Kidney Failure, Chronic / complications
  • Kidney Failure, Chronic / therapy*
  • Lipoprotein(a) / blood*
  • Male
  • Membranes, Artificial
  • Middle Aged
  • Nephelometry and Turbidimetry
  • Polymers
  • Recombinant Proteins
  • Renal Dialysis / instrumentation
  • Renal Dialysis / methods*
  • Serum Albumin / metabolism
  • Sulfones
  • Time Factors
  • Treatment Outcome
  • beta 2-Microglobulin / blood

Substances

  • Biomarkers
  • Endotoxins
  • Hematinics
  • Hemodialysis Solutions
  • Hemoglobins
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-6
  • Lipoprotein(a)
  • Membranes, Artificial
  • Polymers
  • Recombinant Proteins
  • Serum Albumin
  • Sulfones
  • beta 2-Microglobulin
  • Erythropoietin
  • polysulfone P 1700
  • C-Reactive Protein