Inflammatory Response to Sorbent Hemodialysis

Laura Rosales, Stephan Thijssen, Anja Kruse, Murat Hairy Sipahioglu, Padam Hirachan, Jochen G Raimann, Viktoriya Kuntsevich, Mary Carter, Nathan W Levin, Peter Kotanko, Laura Rosales, Stephan Thijssen, Anja Kruse, Murat Hairy Sipahioglu, Padam Hirachan, Jochen G Raimann, Viktoriya Kuntsevich, Mary Carter, Nathan W Levin, Peter Kotanko

Abstract

Inflammation is common and associated with morbidity and mortality in hemodialysis (HD) patients. Exposure to endotoxin contained in the dialysate may trigger inflammation. Dialysate volume is substantially reduced in sorbent HD compared with standard single-pass dialysis. In this prospective study (Clinicaltrials.gov, number: NCT00788905), we compared the inflammatory response to single-pass and sorbent HD. Patients receiving single-pass HD were studied during 1 week of sorbent HD (Allient system; Renal Solutions, Warrendale, PA) and 1 week of single-pass HD. Patients were dialyzed using high-flux polysulfone dialyzers. Midweek pre- and post-HD serum levels of high-sensitivity C-reactive protein, interleukin (IL)-1β, IL-6, IL-10, interferon gamma, tumor necrosis factor alpha (TNF-α), and eotaxin were determined and their intradialytic change corrected for hemoconcentration during single-pass HD and sorbent HD compared by paired t-test. We enrolled 18 patients, nine completed the study. Although TNF-α decreased during both single-pass and sorbent HD (p < 0.001), none of the other biomarkers changed significantly during HD. We observed no difference between single-pass and sorbent HD. For the markers investigated in this study, there was no difference in the acute intradialytic inflammatory response to single-pass or sorbent HD.

Conflict of interest statement

Disclosure: Mary Carter, Peter Kotanko, and Nathan W. Levin hold stocks in Fresenius Medical Care.

Figures

Figure 1.
Figure 1.
Study flow chart. BUN, blood urea nitrogen; HD, hemodialysis.
Figure 2.
Figure 2.
Intradialytic changes of biomarkers of inflammation during single-pass hemodialysis (red), sorbent hemodialysis (green), and the difference between these changes (blue). The data indicate means and 95% confidence intervals. hs-CRP: high-sensitivity C-reactive protein.

References

    1. DePalma JR, Pecker EA, Gordon A, Maxwell MH. A new compact automatic home hemodialysis system. Trans Am Soc Artif Intern Organs. 1968;14:152–159.
    1. Gordon A, Greenbaum MA, Marantz LB, McArthur MJ, Maxwell MH. A sorbent based low volume recirculating dialysate system. Trans Am Soc Artif Intern Organs. 1969;15:347–352.
    1. Gordon A, Better OS, Greenbaum MA, Marantz LB, Gral T, Maxwell MH. Clinical maintenance hemodialysis with a sorbent-based, low-volume dialysate regeneration system. Trans Am Soc Artif Intern Organs. 1971;17:253–258.
    1. Lewin AJ, Gordon A, Greenbaum MA, Maxwell MH. Sorbent based regenerating delivery system for use in peritoneal dialysis. Proc Clin Dial Transplant Forum. 1973;3:126–129.
    1. Jans H, Karn J, Nielsen B, Pleidrup E. Clinical experience with REDY dialysis system. Scand J Urol Nephrol. 1976;(30 Suppl):32–8.
    1. Raja R M, Kramer MS, Rosenbaum JL. Recirculation peritoneal dialysis with sorbent Redy cartridge. Nephron. 1976;16(2):134–42.
    1. Ash SR. The Allient dialysis system. Semin Dial. 2004;17:164–166.
    1. Ash SR. Sorbents in treatment of uremia: A short history and a great future. Semin Dial. 2009;22:615–622.
    1. Rosenbaum BP, Ash SR, Carr DJ. Predicting dialysate sodium composition in sorbent dialysis using single point and multiple-dilution conductivity measurement. ASAIO J. 2005;51:754–760.
    1. Rosenbaum BP, Ash SR, Wong RJ, Thompson RP, Carr DJ. Prediction of hemodialysis sorbent cartridge urea nitrogen capacity and sodium release from in vitro tests. Hemodial Int. 2008;12:244–253.
    1. Agar JW. Review: Understanding sorbent dialysis systems. Nephrology (Carlton) 2010;15:406–411.
    1. Richards N, Ayala JA, Cesare S, et al. Assessment of quality guidelines implementation using a continuous quality improvement programme. Blood Purif. 2007;25:221–228.
    1. Stenvinkel P, Heimburger O, Lindholm B, Kaysen GA, Bergstrom J. Are there two types of malnutrition in chronic renal failure? Evidence for relationships between malnutrition, inflammation and atherosclerosis (MIA syndrome). Nephrol Dial Transplant. 2000;15:953–960.
    1. Stenvinkel P, Heimburger O, Paultre F, et al. Strong association between malnutrition, inflammation, and atherosclerosis in chronic renal failure. Kidney Int. 1999;55:1899–1911.
    1. Stenvinkel P, Lindholm B, Heimbürger M, Heimbürger O. Elevated serum levels of soluble adhesion molecules predict death in pre-dialysis patients: Association with malnutrition, inflammation, and cardiovascular disease. Nephrol Dial Transplant. 2000;15:1624–1630.
    1. Herzog CA, Asinger RW, Berger AK, et al. Cardiovascular disease in chronic kidney disease. A clinical update from Kidney Disease: Improving Global Outcomes (KDIGO). Kidney Int. 2011;80:572–586.
    1. Schiffl H. High-flux dialyzers, backfiltration, and dialysis fluid quality. Semin Dial. 2011;24:1–4.
    1. Economou E, Tousoulis D, Katinioti A, et al. Chemokines in patients with ischaemic heart disease and the effect of coronary angioplasty. Int J Cardiol. 2001;80:55–60.
    1. Emanuele E, Falcone C, D’Angelo A, et al. Association of plasma eotaxin levels with the presence and extent of angiographic coronary artery disease. Atherosclerosis. 2006;186:140–145.
    1. Kaehler J, Tuleweit A, Steven D, et al. Association between eotaxin (CCL11), C-reactive protein, and antimicrobial antibodies in patients undergoing coronary angioplasty. J Investig Med. 2006;54:446–454.
    1. Ash SR, Baker K, Blake DE, et al. Clinical trials of the BioLogic-HD. Automated single access, sorbent-based dialysis. ASAIO Trans. 1987;33:524–531.
    1. Kruse A, Tao X, Bhalani V, et al. Clearance of p-cresol sulfate and β-2-microglobulin from dialysate by commercially available sorbent technology. ASAIO J. 2011;57:219–224.
    1. Schneditz D, Ribistusch W, Schilcher G. Correction of plasma concentrations for effects of hemoconcentration or hemodilution. ASAIO J. 2012;58:160–162.
    1. Caglar K, Peng Y, Pupim LB, et al. Inflammatory signals associated with hemodialysis. Kidney Int. 2002;62:1408–1416.
    1. Herbelin A, Ureña P, Nguyen AT, Zingraff J, Descamps-Latscha B. Elevated circulating levels of interleukin-6 in patients with chronic renal failure. Kidney Int. 1991;39:954–960.
    1. Ward RA. Ultrapure dialysate. Semin Dial. 2004;17:489–497.
    1. Hasuike Y, Nonoguchi H, Ito K, et al. Interleukin-6 is a predictor of mortality in stable hemodialysis patients. Am J Nephrol. 2009;30:389–398.
    1. Panichi V, Migliori M, De Pietro S, et al. C reactive protein in patients with chronic renal diseases. Ren Fail. 2001;23:551–562.
    1. Kaysen GA, Dubin JA, Müller HG, Mitch WE, Rosales L, Levin NW HEMO Group. Impact of albumin synthesis rate and the acute phase response in the dual regulation of fibrinogen levels in hemodialysis patients. Kidney Int. 2003;63:315–322.
    1. Tripepi G, Mallamaci F, Zoccali C. Inflammation markers, adhesion molecules, and all-cause and cardiovascular mortality in patients with ESRD: Searching for the best risk marker by multivariate modeling. J Am Soc Nephrol. 2005;16(Suppl 1):S83–S88.
    1. Kaysen GA, Dubin JA, Müller HG, Rosales LM, Levin NW. The acute-phase response varies with time and predicts serum albumin levels in hemodialysis patients. The HEMO Study Group. Kidney Int. 2000;58:346–352.
    1. Park CW, Shin YS, Kim CM, et al. Increased C-reactive protein following hemodialysis predicts cardiac hypertrophy in chronic hemodialysis patients. Am J Kidney Dis. 2002;40:1230–1239.
    1. Meuwese CL, Halbesma N, Stenvinkel P, et al. Variations in C-reactive protein during a single haemodialysis session do not associate with mortality. Nephrol Dial Transplant. 2010;25:3717–3723.
    1. Pereira BJ, Shapiro L, King AJ, Falagas ME, Strom JA, Dinarello CA. Plasma levels of IL-1 beta, TNF alpha and their specific inhibitors in undialyzed chronic renal failure, CAPD and hemodialysis patients. Kidney Int. 1994;45:890–896.
    1. Tarakçioğlu M, Erbağci AB, Usalan C, Deveci R, Kocabaş R. Acute effect of hemodialysis on serum levels of the proinflammatory cytokines. Mediators Inflamm. 2003;12:15–19.
    1. Stenvinkel P, Ketteler M, Johnson RJ, et al. IL-10, IL-6, and TNF-alpha: Central factors in the altered cytokine network of uremia--the good, the bad, and the ugly. Kidney Int. 2005;67:1216–1233.
    1. Descamps-Latscha B, Herbelin A, Nguyen AT, et al. Balance between IL-1 beta, TNF-alpha, and their specific inhibitors in chronic renal failure and maintenance dialysis. Relationships with activation markers of T cells, B cells, and monocytes. J Immunol. 1995;154:882–892.
    1. Malaponte G, Libra M, Bevelacqua Y, et al. Inflammatory status in patients with chronic renal failure: The role of PTX3 and pro-inflammatory cytokines. Int J Mol Med. 2007;20:471–481.
    1. Rysz J, Banach M, Cialkowska-Rysz A, et al. Blood serum levels of IL-2, IL-6, IL-8, TNF-alpha and IL-1beta in patients on maintenance hemodialysis. Cell Mol Immunol. 2006;3:151–154.

Source: PubMed

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