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Erschienen in: BMC Nephrology 1/2016

Open Access 01.12.2016 | Research article

Vitamins (A, C and E) and oxidative status of hemodialysis patients treated with HFR and HFR-Supra

verfasst von: Simonetta Palleschi, Paolo M. Ghezzi, Giuseppe Palladino, Barbara Rossi, Marino Ganadu, Domenica Casu, Maria Cossu, Giovanni Mattana, Antonio Maria Pinna, Bruno Contu, Tonina Ghisu, Alessandro Monni, Luana Gazzanelli, Maria Cristina Mereu, Franco Logias, Mario Passaghe, Alessandro Amore, Piergiorgio Bolasco, on behalf of the Sardinian Study Group

Erschienen in: BMC Nephrology | Ausgabe 1/2016

Abstract

Background

Hemodiafiltration with on-line endogenous reinfusion (HFR) is an extracorporeal dialytic method that combines diffusion, convection and adsorption. HFR-Supra (HFR-S) is a second-generation system with increased convective permeability and adsorption capability. Previous studies suggested that HFR reduces oxidative stress compared to standard haemodialysis. The principal aim of the present study was to compare antioxidant vitamins behavior and oxidative status of hemodialysis patients treated with HFR and HFR-S.

Methods

The study was designed as a multicenter, randomized, crossover trial. Forty-one patients were recruited from 19 dialysis centers and after a 4-month washout stabilization period in on-line hemodiafiltration (ol-HDF), each patient was randomized to a sequence of treatments (HFR-S followed by HFR or viceversa) with each treatment applied over 6 months. Plasma levels of Advanced Oxidation Protein Products, Total Antioxidant Status, vitamins C, A and E and their ligands (Retinol Binding Protein and total lipids) were measured at baseline and at the end of each treatment period.

Results

Results show that the higher convective permeability of HFR-S with respect to HFR did not produce additional beneficial effects on the patients’ oxidative status, a slight decrease of both Vitamin A and Retinol Binding Protein being the only difference registered in the long-term. However, as compared to ol-HDF, both the re-infusive techniques allowed to reduce the intradialytic loss of Vitamin C and, in the long-term, improve the patients’ oxidative status and increase Retinol Binding Protein plasma values. No significant differences were found between the Vitamin C concentration of pre- and post cartridge UF neither in HFR-S nor in HFR showing that the sorbent resin does not adsorb Vitamin C.

Conclusion

HFR-S and HFR are almost equivalent in term of impact on antioxidant vitamins and oxidative status of hemodialysis patients. Nonetheless, as compared to ol-HDF, both treatments produced a sensible sparing of Vitamin C and may represent a new approach for reducing oxidative stress and related complications in dialysis patients. Long-term effects of re-infusive treatments on patients’ cardiovascular morbidity and mortality need to be evaluated.

Trial registration

ClinicalTrials.gov Identifier NCT01492491, retrospectively registered in 10 December 2011.

Background

Oxidative stress and inflammation are common occurrences in end stage renal disease (ESRD) and are believed to play an important role in the excess cardiovascular morbidity and mortality of these patients [1]. Oxidative stress in ESRD is due to both enhanced oxidative capacity and reduced antioxidant defenses, the latter including impaired enzyme activities and decreased levels of antioxidant vitamins [13]. Vitamin deficiencies in ESRD may originate from diet restriction, reduced absorption by medications and co-morbidities, uremia-related alterations of metabolic pathways and intradialytic losses [3]. Vitamin C (Vit C) is the most abundant and effective water-soluble antioxidant in human plasma. Vit. C deficiency is very common in dialysis patients mainly because of low dietary intake, losses during dialysis and accelerated catabolism [46]. Low levels of Vit C may have clinical consequences and associations with increased cardiovascular morbidity and mortality have been found [7, 8]. Vitamin E (Vit E) and Vitamin A (Vit A) are two fat-soluble plasma antioxidants and are transported in plasma by lipoproteins and retinol binding protein (RBP), respectively. Although inconsistent levels of Vit E levels have been reported in uremic patients [3], the administration of this vitamin has been suggested as a promising therapeutic strategy to limit both oxidative stress and its clinical consequences in hemodialysis patients; however, results obtained to date are contradictory [3, 9, 10]. Vit. A levels are generally increased in ESRD patients, mainly due to homeostatic dysregulation of its plasma carrier, the retinol binding protein (RBP) [3, 11]. Nonetheless, in ESRD patients relatively higher Vit. A concentrations are associated with a survival advantage [12, 13]. The molecular mechanisms underlying such an association have not yet been elucidated, albeit a role in the inhibition of inflammatory response has been hypothesized [12].
The enhanced oxidative capacity in uremia is due, at least in part, to systemic microinflammation and up-regulation of superoxide-producing enzymes [1]. This chronic condition results in structural modification of many plasma components, mainly protein and lipids [14]. These modified molecules, even of large size, might themselves become pro-inflammatory so ultimately leading to a further increase of oxidative stress. The removal of large uremic solutes, by breaking this vicious cycle, can therefore contribute to decrease oxidative stress in ESRD. It is known that large-size uremic solutes can more efficiently be removed by convective dialysis modalities, such as haemodiafiltration (HDF), than by standard haemodialysis (HD). On-line HDF (ol-HDF), performed using high-flux biocompatible membrane and high-quality ultrapure dialysate, has been reported to provide superior reduction in inflammation and oxidative stress than high-flux HD [15, 16]. However, convective techniques may also cause negative effects, including the loss of water-soluble antioxidants and amino acids, which cannot be replaced by reinfusion of the dialysate. In particular, it has been calculated that convective transport in ol-HDF is responsible of one-third of Vit. C loss during dialysis, so limiting the advantages of this techniques in decreasing oxidative stress [6].
Hemodiafiltration with endogenous reinfusion (HFR) is a kind of HDF that utilizes separated convection, diffusion and adsorption (Fig. 1) [17]. The system consist of a two-stage filter to separate convection from diffusion, combined with a sorbent cartridge to regenerate blood ultrafiltrate (UF). The regenerated ultrafiltrate, ie the plasmatic water deprived of those compounds which had bound to the sorbent resin, is reinfused back to the patient between the first and second stage of the filter. The sorbent cartridge contains styrene divinylbenzene (SDVB) hydrophobic resin which has a high affinity for different uremic toxins, cytokines and inflammatory mediators [1821] while it does not retain nutrients like albumin and amino acids [2224]. Hence, this technique allows the removal of medium/large uremic solutes by avoiding at the same time the loss of important nutrients. Previous studies showed that HFR has a better impact on both inflammation and oxidative stress than HD [2528], with an efficacy similar to that of ol-HDF in the long-term reduction of inflammatory markers [29]. Notably, HFR architecture permits to increase convective membrane permeability up to a level which, due to the risk of severe nutrients losses and consequent malnutrition, is not achievable with standard HDF techniques. In the new HFR SUPRA (HFR-S) configuration, the permeability of the first convective chamber was incremented with a new polyethersulfone (PES) hyper high-flux membrane, Synclear 0.2 (Table 1). Uf proteomic analysis showed that Synclear 0.2, as compared to a PES high-flux membrane, allows a better extraction of middle-high molecular weight solutes and protein bound uremic toxins [30, 31]. Based on all the above, one can thus hypothesize that the increased depurative capacity of HFR-S might have a positive impact on the oxidative status of dialysis patients. The present study was designed to verify this hypothesis by comparing HFR and HFR-S treatments as for their short- and long-term effects on plasma levels of Advanced Protein Oxidation Products (AOPP), Total Antioxidant Status (TAS) and antioxidant vitamins C, A, E and their ligands (Retinol Binding Protein, RBP, and total lipids for Vit A and E, respectively). Moreover, since the UF re-infusion would allow sparing (micro)nutrients such as Vit C thereby potentially beneficial effects on patients (anti)oxidative status are produced, a secondary aim of the study was to compare the two re-infusive techniques with the ol-HDF, used in the run-in phase.
Table 1
Characteristics of HFR and HFR-S filters
 
Filter section
HFR
HFR-S
Membrane Type (surface)
convective
PES HF (0.7 m2)
PES HHF (0.7 m2)
Sterilization mode: gamma rays
diffusive
PES LF (1.7 m2)
PES LF (1.7 m2)
Kuf (mL/h/mmHg)
convective
25
39
diffusive
13
13
Albumina sieving coefficient
convective
0.002
0.2
diffusive
<0.0001
<0.0001
Adsorbent cartridge (volume) Sterilization mode: dry steam
 
SDVB (40 mL)
SDVB (80 mL)
PES Polyethersulfone (LF Low flux, HF high flux, HHF Hyper high flux)
SDVB Styrene Divinylbenzene
aBovin Serum Albumin
Finally, we evaluated the sieving coefficient (SC-like) of vit C through the convective membranes and its adsorption on the SDVB resin cartridges at both the start and the end of HFR-S and HFR single sessions.

Methods

Study design and participant characteristics

The study was designed as a prospective, multicenter, crossover trial with centralized randomization (Fig. 2). Between July and December 2011, forty-one ESRD patients were recruited from 19 territorial Dialysis Units of the National Public Health Care Service of Sardinia (Italy); their mean age was 67.0 ± 14.2 years (min 21, max 86); mean dialysis vintage was 101.8 ± 82.2 months. The total duration of the study was 16 months: after a 4-month run-in period in post-dilution ol-HDF by a hollow-fiber dialyzers (PHYLTHER, Bellco S.r.l., Mirandola, Italy) with 1.7 m2 PES HF membrane, each patient was randomized to a sequence of treatments (HFR-S followed by HFR or viceversa) with each treatment applied over 6 months. The randomization procedure was stratified by Center. Twenty-nine patients completed the study: two patients withdrew during the run-in period, further seven and three patients during the first and second treatment period, respectively (Fig. 2). Due to the earthquake that struck Mirandola district in 2012, some logistical problems arose in properly storing the plasma aliquots for AOPP an TAS measurements collected at the end of the second treatment period. Hence, only the values up to the first treatment period are available for these variables.
Inclusion criteria were dialysis vintage longer than 6 months, age > 18 years and well functioning vascular access without recirculation (Qb ≥ 300 mL/min). Exclusion criteria were: residual diuresis > 300 mL/day; significant acute or chronic inflammatory comorbidities; non-renal related anemia; alcohol or drugs abuse; malignant neoplasms; hemoglobinopathy or mielopathy; pregnancy. The causes of ESRD were diabetes (21 %), glomerulonephritis (16 %), interstitial nephrits (9 %), angionephrosclerosis (30 %), polycystic kidney disease (5 %), undeterminated etiology nature (19 %). The majority of patients followed a drug regimen for the control of blood pressure, anemia and secondary hyperparathyroidism. All the subjects were warned to avoid antioxidant supplements thorough all the study.
The extracorporeal dialysis treatment was performed three times per week. All 19 participating Centers made use of ultrapure, sterile and pyrogen-free dialysis solutions checked once monthly by cultural and endotoxins confirmation. Dialysate fluids were produced by a bi-osmosis and purified by daily nocturnal thermal disinfection of the piping (≥90 °C) [3234].

Preparation of collection tubes for Vit C analysis

To prevent the ex vivo degradation of Vit C, a reducing agent (dithioerythritol, DTE, 10 mmol/L final concentration in blood) was added in advance to the collection tubes. 10X DTE in physiological saline solution was prepared just before use, made sterile by filtration (0.22 μm pore size) and added to the tubes for blood and UF withdrawal (0.3 mL for each 3 mL heparinised gel-containing vacutainer and 0.2 mL for each 2 mL amber microcentrifuge tube, respectively). An insulin syringe was used to preserve the vacutainer void. The entire procedure was performed in a sterile environment and was highly reproducible (CV = 1.6 %). The tubes with the additive were stored at 4 °C until use (max 30 days). Preliminary experiments showed that the amount of DTE added did not affected blood cells integrity nor blood rheology up to at least 60 min from the collection, effectively preserving the Vit C content of either plasma or UF up to at least 90 days when specimens were stored at −25 °C [35].

Blood and UF sampling and processing

Blood and pre- and post-cartridge UF samples were collected at any time of the study concomitantly with routine blood tests, both at the beginning and at the end of a first weekly dialysis session. Blood was collected in heparin gel-containing tubes (for vitamins’ assays) and EDTA tubes (for RBP, AOPP and TAS assays) and centrifuged within 30 min from the collection. Gel-containing centrifuged tubes, separated EDTA plasma and UF samples were then immediately frozen (−20 °C). Within 10 days from the collection, the samples were transferred in dry ice to the laboratory where they were stored at −80 °C until analysis (30 days max).

AOPP and TAS assays

Plasma AOPP levels were measured by spectrophotometry on a microplate reader (Bio-Rad 680 XR, Hercules, CA, USA) calibrated with chloramine-T solutions (Sigma-Aldrich, Saint Louis, MO, USA) in the presence of potassium iodide [36]. Absorbance of the reaction mixture was read at 340 nm against a blank solution. Results were expressed as μmol/L of chloramine-T equivalents.
Plasma TAS levels were measured by a commercial colorimetric assay (TAS Randox, County Antrim, UK).

Vit.s C, A, E assays

The determination of Vits C, A and E was carried out by reverse-phase high performance liquid chromatography (Varian model 9010, Varian Medical Systems, Palo Alto, CA, USA) with UV and FL detection, according to previously published methods with some modifications [37, 38]. For Vit C assay, plasma and UF aliquots were extracted with an equal volume of 10 % metaphosphoric acid and the acidic extracts were then separated on a Synergy Polar-RP column (150 mm × 4.6 mm, 4 μm particle size, Phenomenex, Torrance, CA, USA), using 50 mM potassium phosphate buffer at pH 2.5 as mobile phase. For vit.s A and E assay, plasma aliquots were supplemented with the internal standard (6 μmol/L retinyl acetate) and extracted with an equal volume of a mixture of ethyl acetate-butanol (1:1). The separation of organic extracts was then performed on a fully end-capped C18 (150 mm × 4.6 mm, 5 μm particle size, Spherisorb ODS2, Waters Corporation, Milford, MA, USA) using 100 % methanol as mobile phase. Chromatographic runs were performed isocratically at a flow rate of 1.0 mL/min and the column temperature was kept constant at 28 °C.
The eluted compounds were detected spectrophotometrically at 245 nm (Vit C), 292 nm (Vit E) and 325 nm (retinyl acetate) and fluorometrically at 325 nm/475 nm excitation/emission wavelengths (Vit A and retinyl acetate). Chromatograms were analysed by the Galaxie Chromatography Workstation software (version 1.9, Varian Inc.). Sample concentrations were calculated from peak areas by a linear calibration model. The limits of detection, calculated as the analyte concentration corresponding to a signal-to-noise (S/N) ratio of 3, were 0.6 μmol/L, 0.1 μmol/L and 2 μmol/L for Vits C, A and E, respectively. A correction factor was applied to Vit C results to correct for dilution by DTE. The chemicals used were of the highest purity available (Sigma-Aldrich) and the water was ultrapure (Milli-Q water filtration system, Millipore Spa, Rome, Italy).

RBP and total lipids assays

Plasma RBP was determined by a commercial nephelometric assay (BNII, Siemens Healthcare Diagnostics, Tarrytown, NY, USA). Cholesterol and triglycerides were determined by local clinical chemistry laboratories by means of commercial enzymatic methods. Total lipids were calculated as the sum of cholesterol and triglycerides.

Data analysis

The statistical power was verified by the Authors and Biostatistic Specialist of Ethic Committee. All blood values at the end of the dialysis session were corrected for hemoconcentration. Results are expressed as means and standard deviations - or medians and interquartile range depending on the distribution’s normality - for continuous data and as frequency for categorical data. The assumption of normality was checked by the Shapiro-Wilk test. Vitamin levels below the method LOD were assigned a value of ½ LOD. For all the variables but AOPP and TAS, the long-term effects of the treatments were compared by either CROS-analysis [39] (HFR-S vs HFR) or repeated measures ANOVA (HFR vs HFR-S vs run-in) using either parametric or non-parametric tests as appropriate. For AOPP and TAS, paired and unpaired t-test (or, when appropriate, their non-parametric equivalents) were used for comparison within arms and between arms, respectively. As for the acute effects, the percent reduction ratios (RR% = [start session value – end session value] *100/start session value) of the different treatments were compared by either ANOVA or ANCOVA, the latter being used in case of significant correlation between pre-dialysis levels and intra-dialytic losses. Only values ≥ LOD were entered into RR% calculation. Associations were assessed by Spearman rank correlation test. Extreme outliers (more than 3 inter-quartile ranges) were excluded from the statistical tests. P < 0.05 were considered significant and all tests were 2-tailed. Statistical analysis and data plotting were performed by using SigmaPlot ® 12.0 (Systat Software Inc.).

Results and discussion

Patient demographics and clinical characteristics at baseline are reported in Table 2. Study arms were well balanced and no significant biases were introduced by study dropouts at any time (data not shown). The operating conditions and adequacy parameters of the different extracorporeal treatments adopted in the study are reported in Table 3.
Table 2
Personal and clinical data of patients at enrollment
 
All
Arm A
Arm B
n
41
21
20
Age (years)
70 (61–76)
73 (56–79)
67 (65–73)
Dialysis vintage (months)
69 (35–153)
107 (53–164)
60 (29–135)
Gender
M = 26 (63 %)
M = 12 (57 %)
M = 14 (70 %)
F = 15 (37 %)
F = 9 (43 %)
F = 6 (30 %)
Albumin (mg/dL)
3.6 (3.4–3.9)
3.6 (3.4–4.0)
3.7 (3.5–3.9)
Mean Body weight (kg)
M = 63.5 ± 9.6
M = 63.2 ± 7.9
M = 63.8 ± 11.2
F = 56.5 ± 10.5
F = 53.6 ± 10.2
F = 60.7 ± 10.2
BMI
M = 23.7 ± 3.4
M = 24.1 ± 2.3
M = 23.3 ± 4.2
F = 23.8 ± 4.4
F = 23.0 ± 4.1
F = 25.0 ± 4.8
Cardiovascular disease
59 %
62 %
55 %
Hypertension
78 %
81 %
75 %
Diabetes
22 %
19 %
25 %
Charlson Comorbidity Score
6 (6–7)
6 (5–7)
6 (6–7)
Previous dialysis treatment
BHD = 15 (37 %)
BHD = 8 (38 %)
BHD = 7 (35 %)
HDF = 10 (24 %)
HDF = 4 (19 %)
HDF = 6 (30 %)
HFR = 16 (39 %)
HFR = 9 (43 %)
HFR = 7 (35 %)
Continuous data are expressed either as mean ± SD or, in case of not normally distributed data, as median (IQR)
Table 3
Operating conditions and adequacy parameters of the different dialysis treatments adopted in the study
 
ol-HDF (run-in)
HFR-S
HFR
Session length (min)
233 ± 18
235 ± 25
233 ± 16
Qb (mL/min)
313 ± 31
312 ± 31
301 ± 32
Qd (mL/min)
500
500
500
Body weight loss (kg/session)
2.8 ± 0.8
2.7 ± 1.1
2.8 ± 0.9
(Re)infusion volume (L/session)
14.9 ± 2.5
12.9 ± 2.9
13.4 ± 4.1
(Re)infusion rate (mL/min)
64.2 ± 9.6
54.9 ± 13.4
57.5 ± 13.2
eqKt/V
1.22 ± 0.25
1.17 ± 0.32
1.12 ± 0.23
ePCR (g/Kg/day)
1.4 ± 0.6
1.07 ± 0.54
1.08 ± 0.35
Data are expressed as mean ± SD (n = 41, 50 and 50 for ol-HDF, HFR-S and HFR, respectively)
Patients’ biochemical data at the end of the run-in and of each treatment period are reported in Table 4. At the end of the run-in, most of the patients had low Vit. C, high Vit. A and normal Vit. E levels; RBP values were also higher than in non-uremic subjects resulting in lower-than-normal Vit. A/RBP molar ratios; AOPP values were in the normal range, while TAS values were higher-than-normal. For all parameters but AOPP, the levels we found were in agreement with those previously reported for uremic subjects [3, 8, 11, 4042]. At difference, AOPP levels were significantly lower than it was previously reported for these patients [36]. Although this discrepancy could be due, at least in part, to the lack of standardized measurements for AOPP [43], this result suggests that our cohort was characterized by a low level of oxidative damage at baseline. Given that a significant association has been reported between malnutrition and oxidative stress in ESRD [44], the above evidence is in good agreement with and could be partially explained by the good nutritional status of enrolled patients (Table 2). Moreover, the use in all the participating centers of ultrapure dialysate locally produced by biosmosis could also have played a role in decreasing dialysis-related oxidative stress in our patients’ cohort [45].
Table 4
Pre-dialysis levels of antioxidant vitamins and oxidative stress biomarkers at the end of run-in and of either HFR-S or HFR treatments
 
End of run-in
End of HFR-S
End of HFR
Vitamin C (μmol/L)
20.0 (11–32)
21.5 (12–43)
20.0 (10–31)
Vitamin A (μmol/L)
2.8 ± 1.4
2.6 ± 1.0a
3.0 ± 1.2
Vitamin E (μmol/L)
20.2 ± 5.2
20.9 ± 5.9
20.9 ± 5.7
RBP (μmol/L)
5.8 ± 1.4
6.5 ± 1.6a, b
6.9 ± 1.6b
Total lipids (mmol/L)
5.6 ± 1.2
6.1 ± 1.7
6.3 ± 1.7
Vitamin A/RBP (μmol/μmol)
0.47 ± 0.17
0.40 ± 0.11b
0.42 ± 0.13c
Vitamin E/lipids (μmol/mmol)
3.6 ± 0.7
3.6 ± 0. 9
3.4 ± 0.8
AOPP (μmol/L)
28.4 (25–37)
21.7 (20–26)d
-
35.8 (24–45)
-
27.3 (21–34)d
TAS (mmol/L)
1.88 (1.7–2.2)
1.41 (1.3–1.6)d
-
1.99 (1.8–2.2)
-
1.43 (1.4–1.5)d
For all parameters but AOPP and TAS, only patients who completed the study were included in the analysis and cumulative data of the two treatment periods in HFR-S/HFR are represented. For AOPP and TAS only data of the first treatment period were available, hence all patients who reached this stage of the study were included in the analysis. Data are expressed either as mean ± SD or, in case of not normally distributed data, as median (IQR)
a = p < 0.05 vs HFR, n = 29, Cross-analysis [39]
b = p < 0.01 and c = p < 0.05 vs End of run-in, n = 29, ANOVA for repeated measures
d = p < 0.01 vs End of run-in, n = 14 (HFR-S) or 16 (HFR), Wilcoxon Signed Rank Test
At the end of the study, no significant differences were found between HFR-S and HFR as for their long-term effects on Vit C, Vit E, Vit E/lipids, AOPP and TAS levels (Table 4). At difference, significantly lower levels of Vit A and of its plasma carrier, RBP, were measured after HFR-S than after HFR, the Vit A/RBP ratio being not significantly different between the two treatments (Table 4, superscript asterisks). Accordingly, in the short-term, the only significant difference between HFR-S and HFR was the RBP RR% which was higher in HFR-S (Fig. 3). The present results suggest that HFR-S and HFR are equivalent in terms of effects on patients’ oxidative status. The modest difference in Vit A plasma levels did not significantly affect the plasma antioxidant capacity and is easily explained by the difference in the convective permeabilities of the two techniques: the higher convective permeability of HFR-S facilitates the removal of both RBP (MW = 21.2 kDa) and RBP/Vit A complexes from plasma leading to the decrease of the circulating levels of both the protein and its ligand. In fact, at difference of healthy subjects in whom virtually all Vit. A/RBP complexes are bound to prealbumin so preventing the renal loss of this vitamin, Vit. A/RBP complexes unbound to prealbumin are significantly increased in ESRD [40], allowing Vit. A passage trough high-flux membranes and its loss in the outflow dialysate. The evidence that the Vit A /RBP ratio was unchanged between the two treatments substantiates the above interpretation.
It has been demonstrated that the removal of middle-large uremic solutes by convective techniques contribute to decrease oxidative stress in haemodialysis patients [16]. Thus, we can conclude that the beneficial effects on oxidative stress produced by using high-flux membranes in HFR are not significantly improved by using hyper high-flux membranes in HFR-S, ie by further increasing the convective permeability. It could be argued that the low starting levels of AOPP might have decreased the power of the present study and that a higher number of subjects as well as a longer observation period would allow significant differences between HFR and HFR-S to emerge. Although we cannot rule out this possibility, the evidence that AOPP levels significantly decreased during the course of both HFR-S and HFR without significant differences between the two treatments (Table 4, superscript letters) makes this hypothesis unlikely. In fact, as compared to the values reached at the end of the run-in, both treatments induced a significant decrease of both AOPP and TAS and an increase of RBP (but not of vit. A) levels (Table 4, superscript letters). These long-term changes cannot be merely explained by differences in AOPP, TAS and RBP RR%s: actually, the RR%s measured during the run-in sessions (ol-HDF) were similar to those measured during HFR-S and HFR sessions, with the sole exception of RBP, whose RR% was significantly lower in HFR than in either HFR-S or ol-HDF, without significant differences between ol-HDF and HFR-S (Fig. 3). Thus, since RBP levels increased over time during both HFR and HFR-S treatments, it is unlikely that the differences in RR%s play a significant role in this phenomenon. Instead, the above results suggest that, as compared to ol-HDF, during both the re-infusive treatments an homeostatic response took place, consisting of 1) a progressive reduction of systemic oxidative stress accompanied by an adaptative reduction of the plasma antioxidant potential, and 2) an increase of RBP circulating levels.
In our study, ol-HDF, HFR-S and HFR used the same machines, same ultrapure dialysate and same PES membranes, although that used in HFR-S had a higher convective permeability (see Table 1). Thus, in our study the main difference between ol-HDF and HFR-S/HFR consisted in the UF re-infusion. The re-infusion solution is the same plasmatic water of the patient purified on the sorbent cartridge; the composition of this solution depends on the sorbent adsorption capability which is virtually zero with respect to albumin and amino acids and significantly different from zero with respect to some uremic toxins and inflammatory citokines [1824]. In the present study we show for the first time that the sorbent cartridge does not significantly adsorb Vit. C, since no significant differences were found between the Vit.C concentration of pre- and post cartridge UF neither in HFR-S nor in HFR (ns Wilcoxon Signed Rank Test, n = 22 and 26, respectively, Fig. 4). That means that the ultrafiltered Vit C can be entirely returned to the circuit, thereby its intra-dialytic loss is reduced. It has been reported that during a HDF session, both convective and diffusive losses of Vit. C occur, both potentially contributing to the oxidative stress in haemodialysis patients [6]. Accordingly, in the present study we show that the two re-infusive techniques allowed to reduce Vit C RR% by about 15 % as compared to ol-HDF (Fig. 3). Despite the sparing effect produced by each HFR-S/HFR session, we did not find any significant long term increase of Vit. C levels during the treatments (Table 4). This may be due, at least in part, to the high intra- and inter-subject variability of the plasma levels of this vitamin. Nonetheless, it cannot be ruled out that the sparing of Vit. C – and possibly of other small hydrophilic plasma components endowed with antioxidant/nutritional properties – may have played a role in the long-term improvement of oxidative status produced by the two re-infusive treatments.
As for RBP, the present results suggest that, as compared to ol-HDF, both HFR-S and HFR activate endogenous mechanisms of RBP plasma level modulation, likely due to the stimulation of its de novo synthesis. The RBP increase was not associated with a corresponding Vit. A increase, resulting in a net reduction of the Vit. A/RBP ratio (Table 4). This result was rather unexpected, since RBP is physiologically secreted bound to retinol. However, in uremic patients the retinol content of the liver is dramatically reduced [46], thus giving a possible explanation for the above result.
At this time we can only speculate about the biological mechanisms underlying the observed increase of RBP plasma levels. From a physiological point of view, RBP behaves as a negative acute phase protein, ie both inflammation and protein malnutrition depress its hepatic synthesis [4750]. It is known that hemodialysis patients are at higher risk of both inflammation and malnutrition, a large part of them exhibiting an activated acute phase response [51]. Hence, RBP increase might be a consequence of an improvement of patient inflammatory/nutritional status. A previous study did not find significant differences between the circulating levels of some inflammatory markers in HFR and ol-HDF, thus making this hypothesis unlikely [29]. However, it is worth underlying that in the present study RBP increase was accompanied by a significant improvement of patients’ oxidative status and that oxidative stress and inflammation share common pathogenic mechanisms [52]. From a pathological point of view, it should be taken into consideration that in ESRD free RBP and Vit A/RBP complexes are chronically increased, mainly due to the impairment of RBP renal catabolism [11, 40]. Based on an experimental model of AKI, it has been also proposed that a peripheral regulatory signal, normally removed by the kidney, might accumulate in the circulation and upregulate the hepatic release of Vit A/RBP complexes [53]. Thus one can hypothesize that this supposed regulatory signal accumulates in plasma of CKD patients, from where it might be removed by convective transport and, only in case of HFR(−S), be returned to the patient by means of UF re-infusion. In such a way, the stimulus to RBP hepatic release would be lower in ol-HDF than in either HFR-S or HFR. Anyway, regardless of the mechanisms behind the RBP level increase, higher RBP and Vit. A values in hemodialysis patients are associated with a better prognosis, lower values - even still higher than normal values - being strongly associated with higher mortality and cardiovascular risk [12, 13]. With this in mind and considering also that convective dialysis compared to purely diffusive dialysis is supposed to reduce cardiovascular mortality [54], further studies should be undertaken to i) investigate on the long-term impact of different convective techniques on patients’ survival and cardiovascular risk, and ii) better define, if any, the distinctive roles of Vit. A and RBP in the phenomenon.
Finally, we found that, irrespective of the dialysis treatment adopted, i) Vit. C levels were negatively related to the patients’ age and positively related to the vit. A levels (p < 0.01), and, as expected, ii) Vit.s A and E levels were highly correlated to their respective plasma carriers, RBP and total lipids (p < 0.001,Table 5). A strong negative association between Vit. C and age in older people has been previously reported for the general population [55]. Hence, it is likely that physiological mechanisms linked to the elderly rather than to the kidney disease per se are responsible for the above association. The strong association between Vit. C and Vit. A is instead rather surprising since these vitamins are supposed to exert their antioxidant activity in different biological environments; in fact, while Vit. C is a water-soluble antioxidant, Vit. A is a lipid-soluble antioxidant, being significantly less effective than Vit. E in scavenging aqueous radicals [56]. In the general population only a weak interaction was found between Vit. C and Vit. A while a stronger association was found between Vit. C and Vit. E, likely explained by their close physiological interaction [57]. At difference, in our patients Vit. C was significantly related only to Vit. A. If mechanisms other than radical scavenging mediate Vit. C/Vit. A association in ESRD patients deserves further investigation and is beyond the aims of the present study.
Table 5
Significant results of bivariate correlation analysis of antioxidant vitamins and oxidative stress biomarkers pre-dialysis levels at the end of run-in and after a six-months treatment period in HFR-S or HFR
 
End of run-in
End of HFR-S
End of HFR
Vitamin C vs age
−0.626*** (31)
−0.543** (30)
−0.553** (30)
Vitamin C vs Vitamin A
0.476** (31)
0.529** (30)
0.510** (30)
Vitamin A vs RBP
0.841*** (32)
0.613*** (31)
0.616*** (30)
Vitamin E vs total lipids
0.689*** (31)
0.642*** (27)
0.639*** (27)
Analysed parameters included: age, dialysis vintage, Vit C, Vit A, Vit E, RBP, total lipids, Vit A/RBP, Vit E/total lipids, AOPP, TAS. All patients that completed at least the first treatment period were included in the analysis
Data are expressed as rs (n), Spearman correlation test
*p < 0.05; **p < 0.01, ***p < 0.001
Limitations of the present study were the relatively small sample size, the ethnicity of enrolled patients (all from Sardinia, an Italian island housing genetically homogenous populations with traditional living habits) and the lack of measurement of inflammation and uremic retention biomarkers. Further studies overcoming the above limitations will allow to strengthen and expand on the present results.

Conclusion

Kidney failure is associated with oxidative stress. Hemodialysis may contribute to increase oxidative stress of ESRD patients due to the activation of inflammatory pathways and to the loss of small water-soluble antioxidants. Convective dialysis modalities can reduce the burden of oxidative stress of hemodialysis patients by allowing the removal of large pro-oxidant uremic solutes from plasma. Unlike ol-HDF, which is a mixed convective-diffusive method, HFR-S and HFR exploit in sequence convection, adsorption and diffusion. Thanks to the adsorption step, UF is purified by toxic molecules and it can be re-infused to the patient. Since other UF components such as albumin, amino acids and Vit C are not adsorbed, HFR architecture allows to increase convective permeability without the risk of losing useful substances.
In the present study, we show that the higher convective permeability of HFR-S with respect to HFR did not produce additional beneficial effects on the oxidative status of ESRD patients, the only significant difference being a long-term decrease of Vit. A due to the more efficient removal of its plasma carrier, RBP. Further studies are needed to investigate whether the more efficient removal of large molecules by HFR-S produces additional beneficial effects over HFR in term of (micro)inflammation and uremic toxins retention.
In comparison to ol-HDF, both the re-infusive techniques allow to significantly reduce the intradialytic loss of Vit. C and, in the long-term, improve the patients’ oxidative status and increase RBP plasma values, all effects which might have a potentially positive impact on patients’ cardiovascular morbidity and mortality.
Nutrient supplementation is often used to provide malnourished haemodialysis patients with essential aminoacids, vitamins and minerals and/or to counteract the loss of useful substances upon high-convection dialysis techniques. HFR-S and HFR, by returning his own plasmatic water back to the patient, can be a way to restore a more physiological status without additional therapies. Moreover, both the financial and technical costs of nutrient supplementation make HFR definitely more advantageous over other convective techniques with similar depurative capacity. Finally, HFR architecture paves the way for potential, further increase of convective permeability, an improvement otherwise entailing severe loss of plasma proteins which must then be restored by additional infusional therapies.
Ol-HDF has been reported to produce clinical and survival benefits with respect to HD. Nonetheless ESRD patients on convective dialysis still show high levels of inflammation, oxidative stress and high cardiovascular morbidity and mortality. HFR-S and HFR could represent a new biotechnological response potentially able to reduce side effects and complications. The long-term impact of these new techniques on patients’ survival and cardiovascular risk need to be evaluated.

Abbreviations

AOPP, advanced oxidation protein products; DTE, dithioerythritol; ESRD, end stage renal disease; HFR, hemodiafiltration with on-line endogenous reinfusion; HFR-S, HFR-Supra; ol-HDF, on-line hemodiafiltration; PES, polyethersulfone; RBP, retinol binding protein; RR, reduction ratio; SDVB, styrene divinylbenzene; TAS, total antioxidant status; UF, ultrafiltrate; Vit A, vitamin A; Vit C, vitamin C; Vit E, vitamin E

Acknowledgements

We sincerely thank Mrs. Claudia Palazzari for her essential logistic contribution to the fulfillment of the study.
Sardinian Study Group collaborators:
Irene Sitzia 16, Marialuisa Caiazzo 3, Luciangela Calvisi 4, Angelo Piras 5, Annalisa Sini 8, Emiliana Sulis 9, Maria Rosaria Scalas 11, Pierluigi Spiga 13, Andrea Martorana 7, Sabina Fancello 14, Elisa Loiacono 15, Luisa Sereni 3.

Funding

Bellco S.r.l. has supported the laboratory measurements.

Availability of data and materials

The dataset supporting the present findings can be obtained from the study coordinator, dr. Piergiorgio Bolasco (pg.bolasco@tin.it).

Authors’ contributions

SP: made substantial contributions to study conception and design and to data acquisition, analysis and interpretation; performed the statistical analysis and drafted the manuscript. PMG: conceived the study and its design with PG; made substantial contributions to data analysis and interpretation; helped to draft the manuscript and to revise it for important intellectual content. GP: made substantial contributions to data acquisition, analysis and interpretation; helped to draft the manuscript. BR: made substantial contributions to vitamin data acquisition, analysis and interpretation; was involved in drafting the manuscript. MG: made substantial contributions to data acquisition. DC: made substantial contributions to data acquisition. MC: made substantial contributions to data acquisition. GM: made substantial contributions to data acquisition. AMP: made substantial contributions to data acquisition. BC: made substantial contributions to data acquisition. TG: made substantial contributions to data acquisition. AM: made substantial contributions to data acquisition. LG: made substantial contributions to data acquisition. MCM: made substantial contributions to data acquisition. FL: made substantial contributions to data acquisition. MP: made substantial contributions to data acquisition. AA: made substantial contributions to data analysis and interpretation. PB: coordinator of the Polycentric Sardinian Study Group. Conceived the study and its design with PMG; made substantial contributions to data acquisition, analysis and interpretation; helped to draft the manuscript and to revise it for important intellectual content; gave the final approval of the version to be published. All authors read and approved the final manuscript.

Competing interests

Paolo M. Ghezzi is medical-scientific consultant for Bellco S.r.l. (Mirandola-Italy), Giuseppe Palladino is a full time employees of Bellco S.r.l. (Scientific affairs Department and Laboratory Service). The remaining Authors declare no conflict of interest.
Not applicable.
Each enrolled patient was properly informed about the study, including the methods adopted for preserving privacy during collection and transmission of their personal and clinical data; each patient gave his/her written consent to participate. The study was approved by the Ethic Committee of the Cagliari Health Care Service and retrospectively registered at Clinical Trials.gov in 10 December 2011 (NCT01492491).
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.
Literatur
1.
Zurück zum Zitat Vaziri ND. Oxidative stress in uremia: nature, mechanisms, and potential consequences. Semin Nephrol. 2004;24:469–73.CrossRefPubMed Vaziri ND. Oxidative stress in uremia: nature, mechanisms, and potential consequences. Semin Nephrol. 2004;24:469–73.CrossRefPubMed
2.
Zurück zum Zitat Handelman GJ. Vitamin C, deficiency in dialysis patients--are we perceiving the tip of an iceberg? Nephrol Dial Transplant. 2007;22(2):328–31.CrossRefPubMed Handelman GJ. Vitamin C, deficiency in dialysis patients--are we perceiving the tip of an iceberg? Nephrol Dial Transplant. 2007;22(2):328–31.CrossRefPubMed
3.
Zurück zum Zitat Holden RM, Ki V, Morton AR, Clase C. Fat-soluble vitamins in advanced CKD/ESKD: a review. Semin Dial. 2012;25:334–43.CrossRefPubMed Holden RM, Ki V, Morton AR, Clase C. Fat-soluble vitamins in advanced CKD/ESKD: a review. Semin Dial. 2012;25:334–43.CrossRefPubMed
4.
Zurück zum Zitat Raimann JG, Levin NW, Craig RG, Sirover W, Kotanko P, Handelman G. Is vitamin C intake too low in dialysis patients? Semin Dial. 2013;26:1–5.CrossRefPubMed Raimann JG, Levin NW, Craig RG, Sirover W, Kotanko P, Handelman G. Is vitamin C intake too low in dialysis patients? Semin Dial. 2013;26:1–5.CrossRefPubMed
5.
Zurück zum Zitat Zhang K, Dong J, Cheng X, Bai W, Guo W, Wu L, Zuo L. Association between vitamin C deficiency and dialysis modalities. Nephrology (Carlton). 2012;17:452–7.CrossRef Zhang K, Dong J, Cheng X, Bai W, Guo W, Wu L, Zuo L. Association between vitamin C deficiency and dialysis modalities. Nephrology (Carlton). 2012;17:452–7.CrossRef
6.
Zurück zum Zitat Morena M, Cristol JP, Bosc JY, Tetta C, Forret G, Leger CL, et al. Convective and diffusive losses of vitamin C during haemodiafiltration session: a contributive factor to oxidative stress in haemodialysis patients. Nephrol Dial Transplant. 2002;17:422–7.CrossRefPubMed Morena M, Cristol JP, Bosc JY, Tetta C, Forret G, Leger CL, et al. Convective and diffusive losses of vitamin C during haemodiafiltration session: a contributive factor to oxidative stress in haemodialysis patients. Nephrol Dial Transplant. 2002;17:422–7.CrossRefPubMed
7.
Zurück zum Zitat Dashti-Khavidaki S, Talasaz AH, Tabeefar H, Hajimahmoodi M, Moghaddam G, Khalili H, et al. Plasma vitamin C concentrations in patients on routine hemodialysis and its relationship to patients’ morbidity and mortality. Int J Vitam Nutr Res. 2011;81:197–203.CrossRefPubMed Dashti-Khavidaki S, Talasaz AH, Tabeefar H, Hajimahmoodi M, Moghaddam G, Khalili H, et al. Plasma vitamin C concentrations in patients on routine hemodialysis and its relationship to patients’ morbidity and mortality. Int J Vitam Nutr Res. 2011;81:197–203.CrossRefPubMed
8.
Zurück zum Zitat Deicher R, Ziai F, Bieglmayer C, Schillinger M, Horl WH. Low total vitamin C plasma level is a risk factor for cardiovascular morbidity and mortality in hemodialysis patients. J Am Soc Nephrol. 2005;16:1811–8.CrossRefPubMed Deicher R, Ziai F, Bieglmayer C, Schillinger M, Horl WH. Low total vitamin C plasma level is a risk factor for cardiovascular morbidity and mortality in hemodialysis patients. J Am Soc Nephrol. 2005;16:1811–8.CrossRefPubMed
9.
Zurück zum Zitat Lu L, Erhard P, Salomon RG, Weiss MF. Serum vitamin E and oxidative protein modification in hemodialysis: a randomized clinical trial. Am J Kidney Dis. 2007;50:305–13.CrossRefPubMed Lu L, Erhard P, Salomon RG, Weiss MF. Serum vitamin E and oxidative protein modification in hemodialysis: a randomized clinical trial. Am J Kidney Dis. 2007;50:305–13.CrossRefPubMed
10.
Zurück zum Zitat Panichi V, Rosati A, Paoletti S, Ferrandello P, Migliori M, Beati S, et al. A vitamin E-coated polysulfone membrane reduces serum levels of inflammatory markers and resistance to erythropoietin-stimulating agents in hemodialysis patients: results of a randomized cross-over multicenter trial. Blood Purif. 2011;32:7–14.CrossRefPubMed Panichi V, Rosati A, Paoletti S, Ferrandello P, Migliori M, Beati S, et al. A vitamin E-coated polysulfone membrane reduces serum levels of inflammatory markers and resistance to erythropoietin-stimulating agents in hemodialysis patients: results of a randomized cross-over multicenter trial. Blood Purif. 2011;32:7–14.CrossRefPubMed
11.
Zurück zum Zitat Vahlquist A, Peterson PA, Wibell L. Metabolism of the vitamin A transporting protein complex. I. Turnover studies in normal persons and in patients with chronic renal failure. Eur J Clin Invest. 1973;3:352–62.CrossRefPubMed Vahlquist A, Peterson PA, Wibell L. Metabolism of the vitamin A transporting protein complex. I. Turnover studies in normal persons and in patients with chronic renal failure. Eur J Clin Invest. 1973;3:352–62.CrossRefPubMed
12.
Zurück zum Zitat Espe KM, Raila J, Henze A, Krane V, Schweigert FJ, Hocher B, et al. Impact of vitamin A on clinical outcomes in haemodialysis patients. Nephrol Dial Transplant. 2011;26:4054–61.CrossRefPubMed Espe KM, Raila J, Henze A, Krane V, Schweigert FJ, Hocher B, et al. Impact of vitamin A on clinical outcomes in haemodialysis patients. Nephrol Dial Transplant. 2011;26:4054–61.CrossRefPubMed
13.
Zurück zum Zitat Kalousova M, Kubena AA, Kostirova M, Vinglerova M, Ing OM, Dusilova-Sulkova S, et al. Lower retinol levels as an independent predictor of mortality in long-term hemodialysis patients: a prospective observational cohort study. Am J Kidney Dis. 2010;56:513–21.CrossRefPubMed Kalousova M, Kubena AA, Kostirova M, Vinglerova M, Ing OM, Dusilova-Sulkova S, et al. Lower retinol levels as an independent predictor of mortality in long-term hemodialysis patients: a prospective observational cohort study. Am J Kidney Dis. 2010;56:513–21.CrossRefPubMed
14.
Zurück zum Zitat Dhondt A, Vanholder R, Van BW, Lameire N. The removal of uremic toxins. Kidney Int Suppl. 2000;76:S47–59.CrossRefPubMed Dhondt A, Vanholder R, Van BW, Lameire N. The removal of uremic toxins. Kidney Int Suppl. 2000;76:S47–59.CrossRefPubMed
15.
Zurück zum Zitat den Hoedt CH, Bots ML, Grooteman MP, van der Weerd NC, Mazairac AH, Penne EL, et al. Online hemodiafiltration reduces systemic inflammation compared to low-flux hemodialysis. Kidney Int. 2014;86:423–32.CrossRef den Hoedt CH, Bots ML, Grooteman MP, van der Weerd NC, Mazairac AH, Penne EL, et al. Online hemodiafiltration reduces systemic inflammation compared to low-flux hemodialysis. Kidney Int. 2014;86:423–32.CrossRef
16.
Zurück zum Zitat Filiopoulos V, Hadjiyannakos D, Metaxaki P, Sideris V, Takouli L, Anogiati A, Vlassopoulos D. Inflammation and oxidative stress in patients on hemodiafiltration. Am J Nephrol. 2008;28:949–57.CrossRefPubMed Filiopoulos V, Hadjiyannakos D, Metaxaki P, Sideris V, Takouli L, Anogiati A, Vlassopoulos D. Inflammation and oxidative stress in patients on hemodiafiltration. Am J Nephrol. 2008;28:949–57.CrossRefPubMed
17.
Zurück zum Zitat Wratten ML, Ghezzi PM. Hemodiafiltration with endogenous reinfusion. In: Ronco C, Canaud B, Aljama P, editors. Contribution to Nephrology. Basel: Karger AG; 2007. p. 94–102. Wratten ML, Ghezzi PM. Hemodiafiltration with endogenous reinfusion. In: Ronco C, Canaud B, Aljama P, editors. Contribution to Nephrology. Basel: Karger AG; 2007. p. 94–102.
18.
Zurück zum Zitat De Nitti C, Giordano R, Gervasio R, Castellano G, Podio V, Sereni L, et al. Choosing new adsorbents for endogenous ultrapure infusion fluid: performances, safety and flow distribution. Int J Artif Organs. 2001;24:765–76.PubMed De Nitti C, Giordano R, Gervasio R, Castellano G, Podio V, Sereni L, et al. Choosing new adsorbents for endogenous ultrapure infusion fluid: performances, safety and flow distribution. Int J Artif Organs. 2001;24:765–76.PubMed
19.
Zurück zum Zitat Formica M, Morosetti M, Usberti M, Brognoli M, De Simone W, Zito B, et al. Clinical experience in HFR with a new resin-only sorbent cartridge. G Ital Nefrol. 2004;21 Suppl 30:S71–4.PubMed Formica M, Morosetti M, Usberti M, Brognoli M, De Simone W, Zito B, et al. Clinical experience in HFR with a new resin-only sorbent cartridge. G Ital Nefrol. 2004;21 Suppl 30:S71–4.PubMed
20.
Zurück zum Zitat Wratten ML, Sereni L, Lupotti M, Ghezzi PM, Atti M, Formica M. Optimization of a HFR sorbent cartridge for high molecular weight uremic toxins. G Ital Nefrol. 2004;21 Suppl 30:S67–70.PubMed Wratten ML, Sereni L, Lupotti M, Ghezzi PM, Atti M, Formica M. Optimization of a HFR sorbent cartridge for high molecular weight uremic toxins. G Ital Nefrol. 2004;21 Suppl 30:S67–70.PubMed
21.
Zurück zum Zitat Riccio E, Cataldi M, Minco M, Argentino G, Russo R, Brancaccio S, et al. Evidence that p-cresol and IL-6 are adsorbed by the HFR cartridge: towards a new strategy to decrease systemic inflammation in dialyzed patients? PLoS One. 2014;9:e95811.CrossRefPubMedPubMedCentral Riccio E, Cataldi M, Minco M, Argentino G, Russo R, Brancaccio S, et al. Evidence that p-cresol and IL-6 are adsorbed by the HFR cartridge: towards a new strategy to decrease systemic inflammation in dialyzed patients? PLoS One. 2014;9:e95811.CrossRefPubMedPubMedCentral
22.
Zurück zum Zitat De Simone W, De Simone M, De Simone A, Iannaccone S, Manganelli R, Zito B, et al. Aspects of the on-line hemodiafiltration with regeneration and reinfusion of the ultrafiltrate (HFR): multicenter study. G Ital Nefrol. 2004;21 Suppl 30:S161–7.PubMed De Simone W, De Simone M, De Simone A, Iannaccone S, Manganelli R, Zito B, et al. Aspects of the on-line hemodiafiltration with regeneration and reinfusion of the ultrafiltrate (HFR): multicenter study. G Ital Nefrol. 2004;21 Suppl 30:S161–7.PubMed
23.
Zurück zum Zitat Borrelli S, Minutolo R, De Nicola L, Zamboli P, Iodice C, De Paola A, et al. Intradialytic changes of plasma amino acid levels: effect of hemodiafiltration with endogenous reinfusion versus acetate-free biofiltration. Blood Purif. 2010;30:166–71.CrossRefPubMed Borrelli S, Minutolo R, De Nicola L, Zamboli P, Iodice C, De Paola A, et al. Intradialytic changes of plasma amino acid levels: effect of hemodiafiltration with endogenous reinfusion versus acetate-free biofiltration. Blood Purif. 2010;30:166–71.CrossRefPubMed
24.
Zurück zum Zitat Aucella F. Hemodiafiltration with endogenous reinfusion. G Ital Nefrol. 2012;29 Suppl 55:S72–82.PubMed Aucella F. Hemodiafiltration with endogenous reinfusion. G Ital Nefrol. 2012;29 Suppl 55:S72–82.PubMed
25.
Zurück zum Zitat Gonzalez-Diez B, Cavia M, Torres G, Abaigar P, Muniz P. Effect of a hemodiafiltration session with on-line regeneration of the ultrafiltrate on oxidative stress. Comparative study with conventional hemodialysis with polysulfone. Blood Purif. 2008;26:505–10.CrossRefPubMed Gonzalez-Diez B, Cavia M, Torres G, Abaigar P, Muniz P. Effect of a hemodiafiltration session with on-line regeneration of the ultrafiltrate on oxidative stress. Comparative study with conventional hemodialysis with polysulfone. Blood Purif. 2008;26:505–10.CrossRefPubMed
26.
Zurück zum Zitat Calo LA, Naso A, Carraro G, Wratten ML, Pagnin E, Bertipaglia L, et al. Effect of haemodiafiltration with online regeneration of ultrafiltrate on oxidative stress in dialysis patients. Nephrol Dial Transplant. 2007;22:1413–9.CrossRefPubMed Calo LA, Naso A, Carraro G, Wratten ML, Pagnin E, Bertipaglia L, et al. Effect of haemodiafiltration with online regeneration of ultrafiltrate on oxidative stress in dialysis patients. Nephrol Dial Transplant. 2007;22:1413–9.CrossRefPubMed
27.
Zurück zum Zitat Calo LA, Naso A, Davis PA, Pagnin E, Corradini R, Tommasi A, et al. Hemodiafiltration with online regeneration of ultrafiltrate: effect on heme-oxygenase-1 and inducible subunit of nitric oxide synthase and implication for oxidative stress and inflammation. Artif Organs. 2011;35:183–7.PubMed Calo LA, Naso A, Davis PA, Pagnin E, Corradini R, Tommasi A, et al. Hemodiafiltration with online regeneration of ultrafiltrate: effect on heme-oxygenase-1 and inducible subunit of nitric oxide synthase and implication for oxidative stress and inflammation. Artif Organs. 2011;35:183–7.PubMed
28.
Zurück zum Zitat Borrelli S, Minutolo R, De Nicola L, De Simone E, De Simone W, Zito B, et al. Effect of hemodiafiltration with endogenous reinfusion on overt idiopathic chronic inflammation in maintenance hemodialysis patients: a multicenter longitudinal study. Hemodial Int. 2014;18:758–66.CrossRefPubMed Borrelli S, Minutolo R, De Nicola L, De Simone E, De Simone W, Zito B, et al. Effect of hemodiafiltration with endogenous reinfusion on overt idiopathic chronic inflammation in maintenance hemodialysis patients: a multicenter longitudinal study. Hemodial Int. 2014;18:758–66.CrossRefPubMed
29.
Zurück zum Zitat Panichi V, Manca-Rizza G, Paoletti S, Taccola D, Consani C, Filippi C, et al. Effects on inflammatory and nutritional markers of haemodiafiltration with online regeneration of ultrafiltrate (HFR) vs online haemodiafiltration: a cross-over randomized multicentre trial. Nephrol Dial Transplant. 2006;21:756–62.CrossRefPubMed Panichi V, Manca-Rizza G, Paoletti S, Taccola D, Consani C, Filippi C, et al. Effects on inflammatory and nutritional markers of haemodiafiltration with online regeneration of ultrafiltrate (HFR) vs online haemodiafiltration: a cross-over randomized multicentre trial. Nephrol Dial Transplant. 2006;21:756–62.CrossRefPubMed
30.
Zurück zum Zitat Monari E, Cuoghi A, Bellei E, Bergamini S, Caiazzo M, Aucella F, et al. Proteomic analisys of protein extraction during hemofiltration with on-line endogenous reinfusion (HFR) using different polysulphone membranes. J Mater Sci Mater Med. 2014;25:2691–8.CrossRefPubMed Monari E, Cuoghi A, Bellei E, Bergamini S, Caiazzo M, Aucella F, et al. Proteomic analisys of protein extraction during hemofiltration with on-line endogenous reinfusion (HFR) using different polysulphone membranes. J Mater Sci Mater Med. 2014;25:2691–8.CrossRefPubMed
31.
Zurück zum Zitat Cuoghi A, Caiazzo M, Monari E, Bellei E, Bergamini S, Sereni L, et al. New horizon in dialysis depuration: Characterization of a polysulfone membrane able to break the ‘albumin wall’. J Biomater Appl. 2015;29:1363–71.CrossRefPubMed Cuoghi A, Caiazzo M, Monari E, Bellei E, Bergamini S, Sereni L, et al. New horizon in dialysis depuration: Characterization of a polysulfone membrane able to break the ‘albumin wall’. J Biomater Appl. 2015;29:1363–71.CrossRefPubMed
32.
Zurück zum Zitat Alloatti S, Bolasco P, Canavese C, Cappelli G, Pedrini L, Pizzarelli F, et al. Guidelines on water and solutions for dialysis. Italian Society of Nephrology. G Ital Nefrol. 2005;22:246–73.PubMed Alloatti S, Bolasco P, Canavese C, Cappelli G, Pedrini L, Pizzarelli F, et al. Guidelines on water and solutions for dialysis. Italian Society of Nephrology. G Ital Nefrol. 2005;22:246–73.PubMed
33.
Zurück zum Zitat Bolasco P, Contu A, Meloni P, Vacca D, Murtas S. The evolution of technological strategies in the prevention of dialysis water pollution: sixteen years’ experience. Blood Purif. 2012;34:238–45.CrossRefPubMed Bolasco P, Contu A, Meloni P, Vacca D, Murtas S. The evolution of technological strategies in the prevention of dialysis water pollution: sixteen years’ experience. Blood Purif. 2012;34:238–45.CrossRefPubMed
34.
Zurück zum Zitat Bolasco P, Contu A, Meloni P, Vacca D, Galfre A. Microbiological surveillance and state of the art technological strategies for the prevention of dialysis water pollution. Int J Environ Res Public Health. 2012;9:2758–71.CrossRefPubMedPubMedCentral Bolasco P, Contu A, Meloni P, Vacca D, Galfre A. Microbiological surveillance and state of the art technological strategies for the prevention of dialysis water pollution. Int J Environ Res Public Health. 2012;9:2758–71.CrossRefPubMedPubMedCentral
35.
Zurück zum Zitat Rossi B, Tittone F, Palleschi S. Set-up and validation of a convenient sampling procedure to timely and effectively stabilize Vitamin C in blood and plasma specimens stored at routine temperatures. Anal Bioanal Chem 2016, in press, doi:10.1007/s00216-016-9560-6 Rossi B, Tittone F, Palleschi S. Set-up and validation of a convenient sampling procedure to timely and effectively stabilize Vitamin C in blood and plasma specimens stored at routine temperatures. Anal Bioanal Chem 2016, in press, doi:10.​1007/​s00216-016-9560-6
36.
Zurück zum Zitat Witko-Sarsat V, Friedlander M, Capeillere-Blandin C, Nguyen-Khoa T, Nguyen AT, Zingraff J, et al. Advanced oxidation protein products as a novel marker of oxidative stress in uremia. Kidney Int. 1996;49:1304–13.CrossRefPubMed Witko-Sarsat V, Friedlander M, Capeillere-Blandin C, Nguyen-Khoa T, Nguyen AT, Zingraff J, et al. Advanced oxidation protein products as a novel marker of oxidative stress in uremia. Kidney Int. 1996;49:1304–13.CrossRefPubMed
37.
Zurück zum Zitat Nierenberg DW, Lester DC. Determination of vitamins A and E in serum and plasma using a simplified clarification method and high-performance liquid chromatography. J Chromatogr. 1985;345:275–84.CrossRefPubMed Nierenberg DW, Lester DC. Determination of vitamins A and E in serum and plasma using a simplified clarification method and high-performance liquid chromatography. J Chromatogr. 1985;345:275–84.CrossRefPubMed
38.
Zurück zum Zitat Liau LS, Lee BL, New AL, Ong CN. Determination of plasma ascorbic acid by high-performance liquid chromatography with ultraviolet and electrochemical detection. J Chromatogr. 1993;612:63–70.CrossRefPubMed Liau LS, Lee BL, New AL, Ong CN. Determination of plasma ascorbic acid by high-performance liquid chromatography with ultraviolet and electrochemical detection. J Chromatogr. 1993;612:63–70.CrossRefPubMed
39.
Zurück zum Zitat Senn SS. Cross-over Trials in Clinical Research. 2nd ed. John Wiley & Sons; 2003. Senn SS. Cross-over Trials in Clinical Research. 2nd ed. John Wiley & Sons; 2003.
40.
Zurück zum Zitat Kelleher J, Humphrey CS, Homer D, Davison AM, Giles GR, Losowsky MS. Vitamin A and its transport proteins in patients with chronic renal failure receiving maintenance haemodialysis and after renal transplantation. Clin Sci (Lond). 1983;65:619–26.CrossRef Kelleher J, Humphrey CS, Homer D, Davison AM, Giles GR, Losowsky MS. Vitamin A and its transport proteins in patients with chronic renal failure receiving maintenance haemodialysis and after renal transplantation. Clin Sci (Lond). 1983;65:619–26.CrossRef
41.
Zurück zum Zitat Palleschi S, De Angelis S, Diana L, Rossi B, Papa V, Severini G, Splendiani G. Reliability of oxidative stress biomarkers in hemodialysis patients: a comparative study. Clin Chem Lab Med. 2007;45:1211–8.CrossRefPubMed Palleschi S, De Angelis S, Diana L, Rossi B, Papa V, Severini G, Splendiani G. Reliability of oxidative stress biomarkers in hemodialysis patients: a comparative study. Clin Chem Lab Med. 2007;45:1211–8.CrossRefPubMed
42.
Zurück zum Zitat Gerardi G, Usberti M, Martini G, Albertini A, Sugherini L, Pompella A, Di Lorenzo D. Plasma total antioxidant capacity in hemodialyzed patients and its relationships to other biomarkers of oxidative stress and lipid peroxidation. Clin Chem Lab Med. 2002;40:104–10.CrossRefPubMed Gerardi G, Usberti M, Martini G, Albertini A, Sugherini L, Pompella A, Di Lorenzo D. Plasma total antioxidant capacity in hemodialyzed patients and its relationships to other biomarkers of oxidative stress and lipid peroxidation. Clin Chem Lab Med. 2002;40:104–10.CrossRefPubMed
43.
Zurück zum Zitat Selmeci L. Advanced oxidation protein products (AOPP): novel uremic toxins, or components of the non-enzymatic antioxidant system of the plasma proteome? Free Radic Res. 2011;45:1115–23.CrossRefPubMed Selmeci L. Advanced oxidation protein products (AOPP): novel uremic toxins, or components of the non-enzymatic antioxidant system of the plasma proteome? Free Radic Res. 2011;45:1115–23.CrossRefPubMed
44.
Zurück zum Zitat Celik G, Yontem M, Cilo M, Bilge M, Mehmetoglu I, Unaldi M. The relationship between glutathione peroxidase and bioimpedance parameters in nondiabetic hemodialysis patients. Hemodial Int. 2012;16:274–81.CrossRefPubMed Celik G, Yontem M, Cilo M, Bilge M, Mehmetoglu I, Unaldi M. The relationship between glutathione peroxidase and bioimpedance parameters in nondiabetic hemodialysis patients. Hemodial Int. 2012;16:274–81.CrossRefPubMed
45.
Zurück zum Zitat Susantitaphong P, Riella C, Jaber BL. Effect of ultrapure dialysate on markers of inflammation, oxidative stress, nutrition and anemia parameters: a meta-analysis. Nephrol Dial Transplant. 2013;28:438–46.CrossRefPubMed Susantitaphong P, Riella C, Jaber BL. Effect of ultrapure dialysate on markers of inflammation, oxidative stress, nutrition and anemia parameters: a meta-analysis. Nephrol Dial Transplant. 2013;28:438–46.CrossRefPubMed
46.
Zurück zum Zitat Stein G, Schone S, Geinitz D, Abendroth K, Kokot F, Funfstuck R, et al. No tissue level abnormality of vitamin A concentration despite elevated serum vitamin A of uremic patients. Clin Nephrol. 1986;25:87–93.PubMed Stein G, Schone S, Geinitz D, Abendroth K, Kokot F, Funfstuck R, et al. No tissue level abnormality of vitamin A concentration despite elevated serum vitamin A of uremic patients. Clin Nephrol. 1986;25:87–93.PubMed
47.
48.
Zurück zum Zitat Fleck A. Clinical and nutritional aspects of changes in acute-phase proteins during inflammation. Proc Nutr Soc. 1989;48:347–54.CrossRefPubMed Fleck A. Clinical and nutritional aspects of changes in acute-phase proteins during inflammation. Proc Nutr Soc. 1989;48:347–54.CrossRefPubMed
49.
Zurück zum Zitat Baeten JM, Richardson BA, Bankson DD, Wener MH, Kreiss JK, Lavreys L, et al. Use of serum retinol-binding protein for prediction of vitamin A deficiency: effects of HIV-1 infection, protein malnutrition, and the acute phase response. Am J Clin Nutr. 2004;79:218–25.PubMed Baeten JM, Richardson BA, Bankson DD, Wener MH, Kreiss JK, Lavreys L, et al. Use of serum retinol-binding protein for prediction of vitamin A deficiency: effects of HIV-1 infection, protein malnutrition, and the acute phase response. Am J Clin Nutr. 2004;79:218–25.PubMed
50.
Zurück zum Zitat Koch A, Weiskirchen R, Sanson E, Zimmermann HW, Voigt S, Duckers H, et al. Circulating retinol binding protein 4 in critically ill patients before specific treatment: prognostic impact and correlation with organ function, metabolism and inflammation. Crit Care. 2010;14:R179.CrossRefPubMedPubMedCentral Koch A, Weiskirchen R, Sanson E, Zimmermann HW, Voigt S, Duckers H, et al. Circulating retinol binding protein 4 in critically ill patients before specific treatment: prognostic impact and correlation with organ function, metabolism and inflammation. Crit Care. 2010;14:R179.CrossRefPubMedPubMedCentral
51.
Zurück zum Zitat Zimmermann J, Herrlinger S, Pruy A, Metzger T, Wanner C. Inflammation enhances cardiovascular risk and mortality in hemodialysis patients. Kidney Int. 1999;55:648–58.CrossRefPubMed Zimmermann J, Herrlinger S, Pruy A, Metzger T, Wanner C. Inflammation enhances cardiovascular risk and mortality in hemodialysis patients. Kidney Int. 1999;55:648–58.CrossRefPubMed
52.
Zurück zum Zitat Pedruzzi LM, Cardozo LF, Daleprane JB, Stockler-Pinto MB, Monteiro EB, Leite Jr M, et al. Systemic inflammation and oxidative stress in hemodialysis patients are associated with down-regulation of Nrf2. J Nephrol. 2015;28:495–501.CrossRefPubMed Pedruzzi LM, Cardozo LF, Daleprane JB, Stockler-Pinto MB, Monteiro EB, Leite Jr M, et al. Systemic inflammation and oxidative stress in hemodialysis patients are associated with down-regulation of Nrf2. J Nephrol. 2015;28:495–501.CrossRefPubMed
53.
Zurück zum Zitat Gerlach TH, Zile MH. Upregulation of serum retinol in experimental acute renal failure. FASEB J. 1990;4:2511–7.PubMed Gerlach TH, Zile MH. Upregulation of serum retinol in experimental acute renal failure. FASEB J. 1990;4:2511–7.PubMed
54.
Zurück zum Zitat Nistor I, Palmer SC, Craig JC, Saglimbene V, Vecchio M, Covic A, Strippoli GF. Haemodiafiltration, haemofiltration and haemodialysis for end-stage kidney disease. Cochrane Database Syst Rev. 2015;5:CD006258. Nistor I, Palmer SC, Craig JC, Saglimbene V, Vecchio M, Covic A, Strippoli GF. Haemodiafiltration, haemofiltration and haemodialysis for end-stage kidney disease. Cochrane Database Syst Rev. 2015;5:CD006258.
55.
Zurück zum Zitat Woodside JV, Young IS, Gilchrist SE, Vioque J, Chakravarthy U, de Jong PT, et al. Factors associated with serum/plasma concentrations of vitamins A, C, E and carotenoids in older people throughout Europe: the EUREYE study. Eur J Nutr. 2013;52:1493–501.CrossRefPubMed Woodside JV, Young IS, Gilchrist SE, Vioque J, Chakravarthy U, de Jong PT, et al. Factors associated with serum/plasma concentrations of vitamins A, C, E and carotenoids in older people throughout Europe: the EUREYE study. Eur J Nutr. 2013;52:1493–501.CrossRefPubMed
56.
Zurück zum Zitat Palace VP, Khaper N, Qin Q, Singal PK. Antioxidant potentials of vitamin A and carotenoids and their relevance to heart disease. Free Radic Biol Med. 1999;26:746–61.CrossRefPubMed Palace VP, Khaper N, Qin Q, Singal PK. Antioxidant potentials of vitamin A and carotenoids and their relevance to heart disease. Free Radic Biol Med. 1999;26:746–61.CrossRefPubMed
57.
Zurück zum Zitat Schunemann HJ, Grant BJ, Freudenheim JL, Muti P, Browne RW, Drake JA, et al. The relation of serum levels of antioxidant vitamins C and E, retinol and carotenoids with pulmonary function in the general population. Am J Respir Crit Care Med. 2001;163:1246–55.CrossRefPubMed Schunemann HJ, Grant BJ, Freudenheim JL, Muti P, Browne RW, Drake JA, et al. The relation of serum levels of antioxidant vitamins C and E, retinol and carotenoids with pulmonary function in the general population. Am J Respir Crit Care Med. 2001;163:1246–55.CrossRefPubMed
Metadaten
Titel
Vitamins (A, C and E) and oxidative status of hemodialysis patients treated with HFR and HFR-Supra
verfasst von
Simonetta Palleschi
Paolo M. Ghezzi
Giuseppe Palladino
Barbara Rossi
Marino Ganadu
Domenica Casu
Maria Cossu
Giovanni Mattana
Antonio Maria Pinna
Bruno Contu
Tonina Ghisu
Alessandro Monni
Luana Gazzanelli
Maria Cristina Mereu
Franco Logias
Mario Passaghe
Alessandro Amore
Piergiorgio Bolasco
on behalf of the Sardinian Study Group
Publikationsdatum
01.12.2016
Verlag
BioMed Central
Erschienen in
BMC Nephrology / Ausgabe 1/2016
Elektronische ISSN: 1471-2369
DOI
https://doi.org/10.1186/s12882-016-0315-6

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