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      Dialysis with high-flux membranes significantly affects plasma levels of neutrophil gelatinase-associated lipocalin

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      Critical Care
      BioMed Central

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          Abstract

          I read with interest the recent article by Schilder et al. reporting that plasma levels and the biomarker value of neutrophil gelatinase-associated lipocalin (NGAL) in critically ill patients with acute kidney injury (AKI) are not affected by continuous venovenous hemofiltration (CVVH) [1]. Recently, Honore et al. [2] commented on the data by Schilder et al., suggesting that further studies are warranted to definitely assess the membranes and the dialytic techniques that can remove NGAL from plasma and thus affect its accuracy as a marker of AKI. Our results in 31 patients on maintenance hemodialysis (MHD), published in Critical Care as part of a study that evaluated the effect of glomerular filtration rate impairment on diagnostic performance of NGAL [3], appear quite different from those found by Schilder et al. in critically ill patients who received CVVH. Patients on MHD received low-flux dialysis (23 treatments) with a polysulfone membrane (F8; Fresenius, Bad Homburg, Germany), or different high-flux membranes. High-flux dialysis treatments were performed in 13 patients by using a triacetate cellulose membrane with a surface of 1.9 m2 and an ultrafiltration rate (UFR) of 8474 mL/h per 100 mm Hg (N190 FH; Nipro, Osaka, Japan). The remaining eight treatments were performed as hemodiafiltration with a polyphenylene membrane with a surface of 2.0 m2 and a UFR of 6800 mL/h per 100 mm Hg (Phylther; Bellco, Mirandola, Italy) or as an acrylonitril and natrium metallylsulfone copolymer membrane with a surface of 2.15 m2 and a UFR of 6500 mL/h per 100 mm Hg (Nephral 500; Gambro, Lund, Sweden). Dialysis length was 4.0 ± 0.2 h, and blood flow was 312 ± 43 mL/min. Mean plasma concentrations of NGAL increased by 9.1 ± 24.4 % at the end of low-flux dialysis, indicating that low-flux polysulfone did not remove NGAL (Fig. 1). Treatments with high-flux membranes decreased plasma NGAL significantly (P < 0.0001). The reduction ratio of NGAL was higher after hemodiafiltration (52.1 ± 26.7 %) than after high-flux dialysis (26.6 ± 26.1 %, P = 0.053). Fig. 1 Effect of dialysis with low-flux (LF) or high-flux (HF) membranes on plasma concentrations of neutrophil gelatinase-associated lipocalin (NGAL) in 31 patients on maintenance hemodialysis Schilder et al. performed CVVH treatments with a triacetate membrane with a surface of 1.9 m2 (UF-205), a UFR of 3700 mL/h per 100 mm Hg lower than that of our triacetate membrane, and a lower sieving coefficient for middle molecules (0.81 versus 0.91 for myoglobin). During treatments, the blood flow was kept at 180 mL/min and the substitution fluid at 2 L/h. These differences can justify, at least in part, the lower removal of NGAL found in patients with AKI than in patients on MHD. Besides the chemical composition of the membrane, different parameters of the dialysis session may influence the removal of NGAL. Therefore, further studies are warranted to assess the membranes and the dialytic techniques that can affect the accuracy of NGAL as a marker of AKI.

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          Effect of glomerular filtration rate impairment on diagnostic performance of neutrophil gelatinase-associated lipocalin and B-type natriuretic peptide as markers of acute cardiac and renal failure in chronic kidney disease patients

          Introduction Cardio-renal syndromes are characterized by the impairment of cardiac and renal functions. Plasma and urinary neutrophil gelatinase-associated lipocalin (NGAL), and plasma B-type natriuretic peptide (BNP) are markers of acute kidney injury (AKI) and heart failure (HF), respectively. The aim of this study was to assess the effect of the reduction of glomerular filtration rate (GFR) on plasma BNP and on plasma and urinary NGAL concentrations in stable chronic kidney disease (CKD) patients at different functional stages. Methods GFR (99mTc-DTPA), plasma BNP, and plasma and urinary concentrations of NGAL were measured in 310 clinically stable CKD patients, at functional stages from 1 to 5. Serum and urinary low-molecular-weight proteins cystatin C and β2-microglobulin, and urinary tubular enzymes were measured for comparison. Plasma BNP, NGAL, cystatin C and β2-microglobulin were measured also in 31 maintenance hemodialysis patients. Results Plasma NGAL increased with the reduction of GFR in CKD patients from stage 2. In the different CKD stages modest differences were found for BNP values. Urinary NGAL increased slightly but significantly in patients at CKD stages 4 and 5, similarly to urinary cystatin C and β2-microglobulin. In maintenance hemodialysis patients, plasma NGAL and BNP were markedly increased, and high-flux hemodialysis significantly decreased their plasma concentrations. Conclusions Plasma NGAL increases markedly with the reduction in GFR, generating a very high number of false positive diagnoses of AKI in stable CKD patients. The grade of GFR impairment and the cause of kidney disease have a lower effect on urinary NGAL and on plasma BNP. In any case, specific reference values of NGAL and BNP should be used in chronic kidney disease patients, according to their functional stage, when assessing acute kidney injury, heart failure, and cardio-renal syndromes in patients with impaired GFR.
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            The plasma level and biomarker value of neutrophil gelatinase-associated lipocalin in critically ill patients with acute kidney injury are not affected by continuous venovenous hemofiltration and anticoagulation applied

            Introduction Neutrophil gelatinase-associated lipocalin (NGAL) is a biomarker of acute kidney injury (AKI), and levels reflect severity of disease in critically ill patients. However, continuous venovenous hemofiltration (CVVH) may affect plasma levels by clearance or release of NGAL by activated neutrophils in the filter, dependent on the anticoagulation regimen applied. We therefore studied handling of NGAL by CVVH in patients with AKI. Methods Immediately before initiation of CVVH, prefilter blood was drawn. After 10, 60, 180, and 720 minutes of CVVH, samples were collected from pre- and postfilter (in- and outlet) blood and ultrafiltrate. CVVH with the following anticoagulation regimens was studied: no anticoagulation in case of a high bleeding tendency (n = 13), unfractionated heparin (n = 8), or trisodium citrate (n = 21). NGAL levels were determined with enzyme-linked immunosorbent assay (ELISA). Results Concentrations of NGAL at inlet and outlet were similar, and concentrations did not change over time in any of the anticoagulation groups; thus no net removal or production of NGAL occurred. Concentrations of NGAL at inlet correlated with disease severity at initiation of CVVH and at the end of a CVVH run. Concentrations of NGAL in the ultrafiltrate were lower with citrate-based CVVH (P = 0.03) and decreased over time, irrespective of anticoagulation administered (P < 0.001). The sieving coefficient and clearance of NGAL were low and decreased over time (P < 0.001). Conclusions The plasma level and biomarker value of NGAL in critically ill patients with AKI are not affected by CVVH, because clearance by the filter was low. Furthermore, no evidence exists for intrafilter release of NGAL by neutrophils, irrespective of the anticoagulation method applied.
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              Is neutrophil gelatinase-associated lipocalin unaffected by convective continuous renal replacement therapy? Definitely … maybe

              Two recent studies published in Critical Care reported that plasma [1] and urinary [2] levels of neutrophil gelatinase-associated lipocalin (NGAL), an important biomarker for prediction and diagnosis of acute kidney injury, were not affected by continuous renal replacement therapy (CRRT). The investigators assessed NGAL elimination during continuous venovenous hemofiltration [1] and hemodiafiltration [2] using respectively a cellulose triacetate [1] and a polysulfone [2] membrane filter. Of note is that these filters both have notoriously low adsorption capacity [3]. Recently, the proinflammatory high-mobility group box 1 protein, a cytokine with a molecular weight approximating that of NGAL, was also found to be unaffected by convective CRRT. However, it was significantly (up to 90 %!) cleared from the circulation when highly adsorptive membranes (i.e., surface-treated acrylonitrile 69 and polymethylmethacrylate) were used [4]. These membranes are increasingly applied for hemofiltration in critically ill patients [4]. Thus, it is imperative to evaluate NGAL clearance during convective CRRT performed with highly adsorptive membranes before definitively accepting that CRRT leaves the sensitivity of this biomarker intact.
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                Author and article information

                Contributors
                carlo.donadio@med.unipi.it
                Journal
                Crit Care
                Critical Care
                BioMed Central (London )
                1364-8535
                1466-609X
                31 January 2016
                31 January 2016
                2015
                : 20
                : 20
                Affiliations
                Department of Clinical and Experimental Medicine, Division of Nephrology, University of Pisa, Via Savi 10, 56100 Pisa, Italy
                Article
                1198
                10.1186/s13054-016-1198-4
                4733511
                26826870
                13bc7e18-c47e-4318-be9e-49a53d483f7f
                © Donadio. 2016

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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                Funded by: University of Pisa
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                © The Author(s) 2016

                Emergency medicine & Trauma
                Emergency medicine & Trauma

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