American Journal of Kidney Diseases
Volume 52, Issue 1 , Pages 93-101, July 2008

Reduction in β2-Microglobulin With Super-flux Versus High-flux Dialysis Membranes: Results of a 6-Week, Randomized, Double-blind, Crossover Trial

  • Rebecca Pellicano, MBBS, FRACP

      Affiliations

    • Department of Nephrology, Monash Medical Centre, Clayton, Victoria, Australia
    • Department of Medicine, Monash University, Clayton, Victoria, Australia.
    • Corresponding Author InformationAddress correspondence to Rebecca Pellicano, MBBS, FRACP, Department of Nephrology, Monash Medical Centre, 246 Clayton Rd, Clayton, Victoria, Australia, 3168.
  • ,
  • Kevan R. Polkinghorne, BHB, MClinEpi, MBChB, FRACP, PhD

      Affiliations

    • Department of Nephrology, Monash Medical Centre, Clayton, Victoria, Australia
    • Department of Medicine, Monash University, Clayton, Victoria, Australia.
  • ,
  • Peter G. Kerr, MBBS, PhD, FRACP

      Affiliations

    • Department of Nephrology, Monash Medical Centre, Clayton, Victoria, Australia
    • Department of Medicine, Monash University, Clayton, Victoria, Australia.

Received 23 August 2007; accepted 12 February 2008. published online 23 April 2008.

Background

Uremic toxicity is a major concern in the dialysis population. There is keen interest in techniques that increase the removal of larger uremic molecules. We examined the short-term impact of a new, more porous, super-flux Helixone membrane (FX-E) versus the conventional high-flux Helixone membrane (FX-60) on β2-microglobulin (β2M) reduction and nutritional and inflammatory parameters.

Study Design

Randomized, double blind, crossover, pilot trial.

Setting & Participants

A single freestanding dialysis center. 30 stable hemodialysis patients.

Intervention

Patients were treated with FX-60 and FX-E membranes for a treatment period of 6 weeks each, with a 2-week washout period in between.

Outcome & Measurements

Primary outcome was change in β2M concentrations from baseline to end of treatment. Serum samples were obtained predialysis and postdialysis at 0, 2, and 6 weeks, and dialysate albumin samples were collected continuously throughout dialysis sessions.

Results

Mean postdialysis β2M concentrations at the end of 6 weeks of treatment were 6.73 mg/L for FX-E versus 8.22 mg/L for FX-60, which was significantly lower overall by 0.69 mg/L (95% confidence interval [CI], −1.09 to −0.29; P = 0.001). β2M reduction ratios were greater overall with FX-E by 4.83% (95% CI, 2.78 to 6.89; P < 0.001), with mean values of 57% for FX-60 versus 66% for FX-E at the end of treatment. Median dialysate albumin loss with FX-E was 1.23 g (range, 0.22 to 4.83 g) compared with 0.17 g (range, 0.0017 to 2.69 g) with FX-60, which was greater by 1.52 g (95% CI, 1.11 to 1.93; P < 0.001). Serum albumin concentrations were slightly lower with FX-E by 0.1 g/dL (0.55 g/L; 95% CI, −1.04 to −0.07; P = 0.03), but prealbumin concentrations were not significantly different at 8.53 mg/L (95% CI, −23.76 to 6.71; P = 0.3). There were no differences in inflammatory cytokine concentrations or small-solute removal.

Limitations

Short-term pilot study.

Conclusion

In this stable dialysis population, removal of β2M was more efficient with the Helixone super-flux FX-E membrane, with only a small decrease in albumin concentrations despite increased albumin loss. Large trials with longer treatment periods are required to evaluate the impact of the FX-E membrane on clinical outcomes.

Index Words: Middle molecules, hemodialysis, super-flux membranes, albumin, inflammation

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 Originally published online as doi:10.1053/j.ajkd.2008.02.296 on April 15, 2008.

 Trial Registration: www.anzctr.org.au; study number: 12606000132549.

PII: S0272-6386(08)00466-6

doi:10.1053/j.ajkd.2008.02.296

American Journal of Kidney Diseases
Volume 52, Issue 1 , Pages 93-101, July 2008