Next Article in Journal
The Role of Age, Neutrophil Infiltration and Antibiotics Timing in the Severity of Streptococcus pneumoniae Pneumonia. Insights from a Multi-Level Mathematical Model Approach
Next Article in Special Issue
Relation of α2-Antiplasmin Genotype and Genetic Determinants of Fibrinogen Synthesis and Fibrin Clot Formation with Vascular Endothelial Growth Factor Level in Axial Spondyloarthritis
Previous Article in Journal
Phytohormone Abscisic Acid Improves Memory Impairment and Reduces Neuroinflammation in 5xFAD Mice by Upregulation of LanC-Like Protein 2
Previous Article in Special Issue
Effects of Diabetes Mellitus on Fibrin Clot Structure and Mechanics in a Model of Acute Neutrophil Extracellular Traps (NETs) Formation
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJMS
Volume 21
Issue 22
10.3390/ijms21228426
ijms-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Terminal Phase Components of the Clotting Cascade in Patients with End-Stage Renal Disease Undergoing Hemodiafiltration or Hemodialysis Treatment

by
Krisztina Pénzes
1,
Boglárka Hurják
1,
Éva Katona
1,
Gergely Becs
2,
József Balla
2 and
László Muszbek
1,*
1
Division of Clinical Laboratory Science, Department of Laboratory Medicine, University of Debrecen, Faculty of Medicine, H-4032 Debrecen, Hungary
2
Department of Nephrology, University of Debrecen, Faculty of Medicine, H-4032 Debrecen, Hungary
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2020, 21(22), 8426; https://doi.org/10.3390/ijms21228426
Submission received: 1 October 2020 / Revised: 25 October 2020 / Accepted: 5 November 2020 / Published: 10 November 2020
(This article belongs to the Special Issue Fibrinogen/Fibrin, Factor XIII and Fibrinolysis in Diseases)
Browse Figures
Versions Notes

Abstract

:
Hemostasis disorder in patients with end-stage renal disease (ESRD) is frequently associated with bleeding diathesis but it may also manifest in thrombotic complications. Analysis of individual coagulation and fibrinolytic factors may shed light on the background of this paradox situation. Here we explored components essential for fibrin formation/stabilization in ESRD patients being on maintenance hemodiafiltration (HDF) or hemodialysis (HD). Pre-dialysis fibrinogen, factor XIII (FXIII) antigen concentrations and FXIII activity were elevated, while α2-plasmin inhibitor (α2PI) activity decreased. The inflammatory status, as characterized by C-reactive protein (CRP) was a key determinant of fibrinogen concentration, but not of FXIII and α2PI levels. During a 4-h course of HDF or HD, fibrinogen concentration and FXIII levels gradually elevated. When compensated for the change in plasma water, i.e., normalized for plasma albumin concentration, only FXIII elevation remained significant. There was no difference between HDF and HD treatments. Individual HDF treatment did not influence α2PI activity, however after normalization it decreased significantly. HD treatment had a different effect, α2PI activities became elevated but the elevation disappeared after normalization. Elevated fibrinogen and FXIII levels in ESRD patients might contribute to the increased thrombosis risk, while decreased α2PI activity might be associated with elevated fibrinolytic potential.

1. Introduction

End-stage renal disease (ESRD) is the final outcome of a variety of chronic kidney diseases, which requires hemodiafiltration (HDF)/hemodialysis (HD) treatment or kidney transplantation for survival. HD removes low molecular weight uremic toxins simply by diffusion, while HDF, although it uses the same type of dialyzer with the same pore size as HD, employs convective transport resulting in the excretion of small to mid-size toxic proteins, as well [1,2]. In general, ESRD is considered to be associated with risk of bleeding partly due to impaired platelet function [3,4,5,6,7]. However, paradoxically, thrombotic manifestations involving both the arterial and the venous side are also rather common in this patient group [8,9,10,11,12]. Such thrombotic complications include ischemic stroke, myocardial infarction, peripheral artery occlusion, deep vein thrombosis, pulmonary embolism and vascular access thrombosis. The coincidence of hemorrhagic diathesis and thrombotic tendency suggests a complex imbalance in the clotting system, platelet function and changes in the fibrinolytic system also contribute to the hemostatic alterations [13,14]. Individual variations in the conditions and treatment of ESRD patients might contribute to the variability of clinical hemostatic symptoms. General functional tests and determination of various hemostatic parameters have been both used to characterize the hemostatic balance of ESRD patients and explore the pathomechanism leading to altered hemostasis. Concerning the clotting system investigations mainly targeted its activation leading to increased thrombin generation. In ESRD patients undergoing regular hemodialysis markers of thrombogenesis including thrombin-antithrombin complex, prothrombin fragment 1.2, D-dimer, fibrinopeptide A, and factor VIII became elevated, suggesting intravascular activation of the coagulation cascade [15,16].
In the present study we were interested how the constituents of the final stage of clotting cascade are influenced by ESRD and its treatment modality. Fibrinogen, factor XIII (FXIII) and α2-plasmin inhibitor (α2PI) are the key player in the formation of fibrin clot and its stabilization. Thrombin generated as the end-result of activated clotting system transform fibrinogen into fibrin monomers by cleaving off fibrinopeptides A and B from the parent molecule. Fibrin monomers spontaneously polymerize to become fibrin clot insoluble in plasmatic conditions. FXIII is of tetrameric structure consisting of two potentially active A subunits (FXIII-A) and two protective/inhibitory B subunits (FXIII-B). Thrombin removes an activation peptide of 37 amino acids from the N-terminus of FXIII-A and in the presence of Ca2+ the truncated FXIII-A assumes an enzymatically active configuration. Active FXIII (FXIIIa) is a transglutaminase that cross-links fibrin α-, and γ-chains by isopeptide bonds and α2PI, the main fibrinolysis inhibitor, to fibrin α-chains. This way it makes fibrin resistant to the shear stress of circulating blood and to proteolytic breakdown by the fibrinolytic system (reviewed in [17,18,19,20,21,22]). Sporadic results on changes of fibrinogen, FXIII and α2PI in ESRD have been reported [6,23,24,25,26,27,28,29]; however, comprehensive analysis of these constituents in ESRD is still missing.
The aim of the present study was to explore novel aspects concerning components important in fibrin formation and stabilization of the fibrin clot in ESRD patients. We determined fibrinogen and FXIII antigen concentrations, FXIII and α2PI activities in ESRD patients and compared the effect of HDF and HD treatments. It was also investigated if inflammation, tested by C-reactive protein (CRP) measurement, influenced these parameters, and if fibrinogen concentration was associated with other investigated parameters. The effects of further variables were also studied, like patient’s age, gender, length of dialysis treatment. While in the first part of the study, the long-term combined effects of ESRD and its treatment by HDF or HD were investigated, in the second part the short-term effect of an actual HDF or HD treatment was studied. In the latter case, changes of fibrinogen, FXIII and α2PI levels were monitored during the four-hour HDF and HD treatments. To take the decrease in plasma water during the dialysis treatments and its effect on protein concentrations into account, the above parameters corrected for albumin concentration were also calculated.

2. Results

2.1. Plasma Fibrinogen and CRP Concentration of ESRD Patients

In 56.6% of ESRD patients being on HDF treatment fibrinogen concentration was above the reference interval (1.5–4.0 g/L), mean fibrinogen concentration was 4.21 ± 0.82 g/L (Figure 1A). Modality switching from HDF to HD treatment did not influence the fibrinogen concentration significantly. In 50.0% of HD-treated patients it remained above the reference interval, mean: 4.23 ± 0.87 g/L. It is to be noted that even fibrinogen values that felt in the reference interval concentrated predominantly in the upper half of the interval.
As fibrinogen is an acute phase protein and ESRD patients frequently suffer from inflammatory conditions, the concentration of CRP, an excellent marker of inflammatory reactions, was also measured (Figure 1B) and its correlation with fibrinogen concentration (Figure 1C,D) was evaluated. In 56.6% of the patients on HDF treatment, the CRP level was above the upper limit of reference interval (females: 4.6 mg/L, males: 5.2 mg/L). The median CRP plasma concentration of ESRD patients was 5.95 mg/L, with interquartile range (IQR): 4.02–15.15 mg/L and there were a few outliers. The CRP level of four HDF treated patients was above 50 mg/L, due to acute inflammatory conditions. Their results are depicted by asterisks not only in Figure 1B, but also in figures demonstrating the results obtained for other investigated parameters. In spite of the few individual changes during the two-week period of HD treatment, the CRP levels, in general, did not change significantly. In 53.0% of the patients it remained above the upper limit of reference interval (median: 4.75 mg/L, IQR: 2.52–14.33 mg/L). As shown in Figure 1C,D fibrinogen concentration was an exponential function of CRP level. The high coefficients of determination (r2: 0.647 and 0.671 in case of HDF and HD treated patients, respectively) demonstrate significant correlation (p < 0.001) between the inflammatory condition and fibrinogen levels. Neither the length of HDF treatment period (r2: 0.018, p = 0.590) or the age of patients (r2: 0.035, p = 0.267) correlated significantly with the fibrinogen levels (not shown in Figure 1). There was no significant difference between females and males in the pre-dialysis fibrinogen and CRP concentrations.

2.2. Factor XIII Activity and Antigen Concentration in the Plasma of ESRD Patients

A key component of the last stage of coagulation cascade is FXIII which circulates in association with fibrinogen and in activated form, it works on fibrin by cross-linking fibrin chains and α2PI to fibrin. In the following experiments, we investigated whether the concentration of FXIII and α2PI which are essential for maintaining normal hemostasis and are involved in the pathomechanism of thrombotic diseases, changes in ESRD. FXIII was measured both by functional test (Figure 2A) and antigen assay (Figure 2B). Similar results were obtained by the two measurement techniques as it was demonstrated by the coefficients of determination both in the HDF (r2: 0.876, p < 0.001) and in the HD (r2: 0.916, p < 0.001) group (Figure 2C,D). In the HDF group the mean FXIII activity was 127.1 ± 27.3% and the mean FXIII antigen concentration was 25.9 ± 5.6 mg/L (Figure 2A,B). Two weeks of hemodialysis treatment did not change significantly the FXIII values (FXIII activity: 134.0 ± 29.8%, FXIII antigen: 27.1 ± 6.7 mg/L). The means in all cases were in the upper tertile of the reference interval. In the HDF group 27% of individual FXIII activity values and 33% of FXIII antigen values exceeded the upper limit of the reference interval. In the HD group 43% (activity) and 40% (antigen) were above the reference interval. These results indicate that in ESRD patients, as compared to healthy individuals, FXIII concentration becomes elevated. Both FXIII activity (r2: 0.132, p = 0.061) and antigen (r2: 0.147, p = 0.070) showed weak nonsignificant correlation with the patients’ age (Figure 2E,F). The length of HDF treatment did not correlate with FXIII levels (r2: 0.004, p = 0.769 for FXIII activity and r2: 0.003, p = 0.272 for FXIII antigen). Neither fibrinogen nor CRP concentration influenced FXIII activity or antigen levels significantly in HDF treated patients (r2: 0.001 and <0.001 for fibrinogen, r2: 0.007 and 0.004 for CRP). Results of the latter parameters are not shown in Figure 2. There was no gender-specific difference in the FXIII activity/concentration of HDF- or HD-treated patients.

2.3. α2-Plasmin Inhibitor Activity in the Plasma of ESRD Patients

In contrast to fibrinogen and FXIII, α2PI activity of ESRD patients tended to be lower than in healthy individuals (Figure 3A). The mean value both in the HDF and HD groups was in the lowest tertile (91.5 ± 17.7% and 87.3 ± 11.9%). 23% of HDF patients and 27% of HD patients demonstrated α2PI activity below the lower limit of the reference intervals. The age of ESRD patients (Figure 3B) negatively correlated with this parameter (r2: 0.304, p = 0.002), while the length of HDF treatment was without effect (r2: <0.001). Actual inflammation, as detected by lack of correlation with CRP levels did not influence α2PI activity. No significant difference of α2PI activity was observed between male and female ESRD patients.

2.4. Changes of Plasma Fibrinogen Concentration during Hemodiafiltration and Hemodialysis Treatments of ESRD Patients

The above results demonstrate the long-term effect of HDF and HD treatments on three key terminal phase components of the hemostasis system. A further interesting question was whether these parameters change during the four-hour individual HDF or HD treatment. As the relation of plasma water and plasma proteins significantly changes during the four-hour treatments, such changes were monitored by the determination of albumin concentrations and results of hemostasis parameters corrected for albumin concentration were also calculated. As expected, albumin concentration gradually elevated during the 4-h HDF and HD treatments. In HDF treated patients, pre-dialysis albumin concentration (median: 37 g/L, IQR: 35–40 g/L) became significantly elevated after 4-h HDF treatment (median: 42 g/L, IQR: 38–44 g/L, p < 0.001). In the HD group a similar elevation was observed (pre-dialysis median albumin concentration: 39 g/L, IQR: 36–41 g/L; post-dialysis median albumin concentration: 44 g/L, IQR: 40–48 g/L, p < 0.001). Similarly, plasma concentration of fibrinogen also became significantly elevated during the four-hour treatments (Figure 4A,B). When corrected for albumin concentration the differences between the fibrinogen levels measured before and after the 4-h treatment disappeared (Figure 4C,D), i.e., the measured elevations were due to the relative decrease of plasma water and not to the elevated amount of fibrinogen in the plasma.

2.5. Changes of Plasma FXIII Activity during Hemodiafiltration and Hemodialysis Treatments of ESRD Patients

In case of FXIII the situation was different (Figure 5). FXIII activity noncorrected for albumin also showed marked elevation during both HDF and HD treatments (Figure 4A,B), however, a statistically significant elevation still remained after correction (Figure 4C,D). The change of FXIII antigen levels was identical to the changes in FXIII activity (not shown).

2.6. Changes of Plasma α2-Plasmin Inhibitor Activity during Hemodiafiltration and Hemodialysis Treatments of ESRD Patients

Interestingly, as opposed to changes in noncorrected fibrinogen and FXIII levels noncorrected α2PI activities (Figure 6A) remained the same during the 4-h HDF treatment. This finding suggested that HDF treatment decreased α2PI level by some mechanisms and the elevation which could have been caused by the decrease of plasma water was counteracted the decrease in the α2PI level. Indeed, when α2PI activity was normalized to albumin concentration its decrease became evident (Figure 6C). As opposed to HDF treatment, the effect of decreased plasma water due to HD treatment resulted in the elevation of α2PI activities (Figure 6B). Like in the case of fibrinogen concentration (Figure 4D), the elevations disappeared when the results were normalized to plasma albumin concentration (Figure 6D).

3. Discussion

The aim of the present study was twofold: First, to explore the effect of long-term hemodialysis treatment on the activity/concentration of fundamental components of the final stage of coagulation cascade in ESRD patients and to compare the two hemodialysis modalities, HDF and HD in this respect. Second, to study their short-term effect, i.e., to monitor individual changes during the four-hour dialysis regimens. The three components selected for the study, fibrinogen, FXIII and α2PI, work together in determining the amount and quality of fibrin clot and its fate in the circulation. It is to be noted that the duration of HD treatment was only two weeks as opposed to the several months or years of HDF treatment. This is a limitation of the study concerning the long-term effect; however, such a study plan made it possible to switch modalities and use the same cohort of ESRD patients for testing the effect of both treatments on the same groups of individuals. Another limitation is the relatively low number of patients enrolled for the study. This is partly due to the exclusion of ESRD patients with co-morbidities that were suspected to influence the plasma level of investigated hemostasis parameters independently. Still, it is realized that further investigations on a higher number of patients would strengthen the conclusion.
Fibrinogen is the precursor protein of fibrin clot and beside its fundamental role in hemostasis it also plays an important role in wound healing. Its expression is controlled by the activity of promoters which contain binding sites for hepatocyte transcription factors, including proteins which influence fibrinogen transcription in response to acute-phase inflammatory stimuli [30]. Elevated fibrinogen concentration is an independent risk factor for atherothrombotic diseases like hemorrhagic stroke and ischemic heart disease [31,32,33,34]. Most studies reported elevated pre-dialysis fibrinogen concentration in ESRD patients on chronic HD treatment [24,27,28,35,36,37], although in part of them the elevation did not reach the level of statistical significance [6,38]. Our results (Figure 1A) also demonstrate considerable elevation of fibrinogen concentration in pre-dialysis samples; in 56.6% HDF patients and in 50.0% of HD patients plasma fibrinogen was above the reference interval. These values agree with those of Zoccali et al., who reported 56% pre-dialysis fibrinogen values being above the reference interval [28]. There was no significant difference between the effect of the two modalities. In case of both modalities, pre-dialysis fibrinogen levels and CRP levels were closely associated, and the high coefficients of determinations suggest that at least in part increased synthesis of acute phase proteins is responsible for the elevated fibrinogen levels (Figure 1C,D). Other investigated variables, like the length of dialysis treatment, age and gender did not seem to influence pre-dialysis plasma fibrinogen concentration.
The pre-dialysis values are determined by longer lasting effects on fibrinogen synthesis, the acute effect of a single dialysis treatment is very likely influenced by other fast acting factors. Derosa et al. also investigated the acute effect of single HDF or HD treatment in ESRD patients on fibrinogen concentration [39]. In patients with type 2 diabetes, HDF but not HD decreased post-dialysis fibrinogen concentrations. In euglycemic subjects, the decrease was not statistically significant. We observed a gradual elevation of fibrinogen levels during HDF as well as HD treatment (Figure 4A,B). These elevations were likely associated with the loss of plasma water during dialysis; fibrinogen concentrations corrected for albumin level failed to increase during dialysis treatments (Figure 4C,D).
Sporadic studies addressed FXIII levels in a few ESRD patients being on maintenance hemodialysis treatment. FXIII activity was determined by functional assay only in a single case [25], and in three cases FXIII-A antigen concentration was measured [23,24,25]. Normal pre-dialysis FXIII activity and FXIII-A antigen was reported by Kolb et al. [25], while significantly elevated FXIII-A concentrations were observed in two other studies [23,24]. We determined FXIII activity and the concentration of FXIII-A2B2 complex in parallel and both parameters were elevated in this patient group. In theory, FXIII activity and FXIII-A antigen could be influenced by proteolytic degradation of FXIII-A and free circulating elastase released by polymorphonuclear leukocytes primed during hemodialysis [40] is capable of degrading FXIII-A [41]. FXIII-A antigen assays could also measure degradation products. For this reason, we selected an immunoassay that measures the complex FXIII tetramer with full activity. The close correlation of FXIII activity and FXIII-A2B2 antigen (Figure 2C,D) suggest that fully active intact FXIII was measured by the immunoassay. During the 4-h HDF and HD treatments, the FXIII activity became significantly elevated (Figure 5A,B). However, as opposed to fibrinogen levels after correction for albumin concentration FXIII activities still remained elevated although the level of significance somewhat decreased. This finding suggests that the decrease of plasma water itself does not explain the elevated FXIII levels and further studies are needed to reveal the mechanism of FXIII elevation in ESRD patients being on hemodialysis treatment. Kolb et al. demonstrated a decrease in plasma FXIII activity, but not in FXIII-A antigen level during HD treatment [25]. However, heparin introduced in the course of HD treatment into the plasma inhibited thrombin used for FXIII activation in activity measurements and resulted in underestimation of FXIII activity. The Technoclone kit we used for FXIII activity measurement contains polybrene that neutralized the effect of heparin.
The two types of FXIII subunits are originated from different cellular sources. FXIII-B is synthesized by hepatocytes, while FXIII-A is present in platelets, monocytes and macrophages [20]. A recent study identified resident macrophages as the major source of circulating FXIII-A [42]. In the plasma the overwhelming majority of FXIII-A subunit forms noncovalent tetrameric complex with FXIII-B, which is present in excess [43]. The formed A2B2 complex then circulates in association with fibrinogen [44,45,46]. In healthy individuals, age and fibrinogen concentration significantly correlated with FXIII activity and FXIII-A2B2 antigen concentration [47]. In ESRD patients there was also a weak correlation between FXIII values and the patients’ age (Figure 2E,F), but very likely due to the relatively low patients’ number the p values were only close to the level of significance. It is interesting that in the healthy population there was relatively weak, but statistically significant correlation between FXIII and fibrinogen concentration, while in ESRD patients this association completely disappeared. As opposed to fibrinogen, FXIII, is not an acute phase protein, which is also demonstrated by the lack of association between FXIII and CRP levels. It is suspected that due to the robust influence of inflammatory status on the fibrinogen concentration the association between fibrinogen and FXIII concentration became concealed in ESRD patients.
It is an intriguing question if elevated FXIII level in ESRD patients represents a risk of atherothrombotic or thromboembolic diseases. This presumption has been tested in a few studies, but no general conclusion could be drawn, so far. There are indications that it might confer increased thrombotic risk to certain subpopulations. For instance, elevated FXIII levels were associated with an increased risk of myocardial infarction and peripheral artery disease in females, but not in males [48,49]. Young patients with the history of myocardial infarction had elevated FXIII activity and antigen levels [50]. Similarly, to atherothrombotic diseases elevated FXIII activity and complex antigen levels conferred an increased risk of venous thromboembolism to females, which remained significant after adjustment for a number of variables [51]. In contrast, only a weak association was observed in the male population. A new clinical study involving larger number of patients could shed light on the association of elevated FXIII levels with thromboembolic and atherothrombotic complications.
α2PI (also called α2-antiplasmin) is a 70 kDa glycoprotein that exists in the plasma in multiple forms due to genetic variation and posttranslational proteolytic modifications (reviewed in [52]). It inhibits circulating plasmin and if cross-linked to fibrin by FXIIIa, it protects fibrin from fibrinolytic degradation [20,52]. Its importance in hemostasis is clearly shown by the severe bleeding diathesis of patients with congenital α2PI deficiency [53]. There are only a few studies on the association of α2PI with thrombotic diseases. A clinical study demonstrated that elevated α2PI levels were independently associated with the risk of myocardial infarction in men [54]. Age-, sex- and race-adjusted hazard ratios for the highest and lowest quartiles demonstrated a protective effect of elevated α2PI against ischemic stroke in the ARIC (Atherosclerosis Risk in Communities) study [55]. However, after multivariate analysis including other clinical variables the standardized hazard ratio did not remain significant. In a mouse model elevation of α2PI levels in the blood worsened the consequences and the outcome of microvascular brain thrombosis and impaired the benefit of thrombolytic treatment, while decrease or lack of α2PI had the opposite effect [56]. Furthermore, elevated α2PI impaired the effectivity of thrombolysis induced by tissue plasminogen activator. Similar findings were reported for mice with acute pulmonary embolism [57].
We found only three studies in which α2PI activity was measured in ESRD patients being on HD [24,26,58]. Only one of them reported post-dialysis values and the effect of HDF has not been investigated. Our results, i.e., the mean pre-dialysis α2PI activities were in the lowest tertile of the refence interval and a significant number of the results was below the reference interval. In this respect there was no significant difference between HDF and HD treatments. These results together with those of two earlier studies [24,58] suggest that long term HDF or HD treatment of ESRD patients decreases the plasma concentration of active α2PI. Monitoring the short-term effect of HDF and HD treatments revealed an interesting difference between the two modalities. α2PI activities not corrected for plasma albumin concentration did not change during the course of an HDF treatment, while they became significantly elevated after a 4-h HD treatment. Correction for albumin considerably altered the situation. In HDF treated patients α2PI activities normalized to albumin concentration decreased, while the elevation observed in HD treated patients disappeared. This finding suggests that the mechanisms operating in HDF treated patients and resulting in decreased α2PI activity normalized to albumin do not function in case of HD treatment. It is to be noted that Vasiri et al. also found elevated α2PI activities after HD treatment; however, a change in plasma water during dialysis was not taken into account in their study [24].

4. Materials and Methods

4.1. Patients and Blood Sampling

Thirty ESRD patients (15 females and 15 males) on chronic dialysis treatment were enrolled for the study. Their age was in the range of 18–70 years (median: 57 years, interquartile range: 41.5–64.5 years). Patients’ data are summarized in the Supplementary Table. Patients with diabetes mellitus, malignant disease and hematological or hemostasis disorders were excluded. At the time of recruiting, the ESRD patients were on the HDF treatment—the preferred modality in our dialysis center—for at least twelve months (median period of HDF treatment: 54 months, interquartile range: 33–108 months). During the investigations there was a modality change, for two weeks the patients were switched to HD treatment, after which the HDF treatment was reinstalled. The dialysis sessions were provided three times a week and one session lasted for effective 240 min for both treatment modalities. Further details of HDF and HD treatments have been described in a previous publication [5] and also in the Supplementary Materials. Before, one and four hours after the actual HDF or HD treatment peripheral blood samples were drawn from the efferent line port into vacutainer tubes (Becton Dickinson, Franklin Lakes, NJ, USA) containing 0.109 mol/L sodium citrate. Plasma from citrated blood was separated by centrifugation (1500× g, 20 min, 4 °C), aliquots of plasma samples were stored at −70 °C until further analysis. The study protocol fully complied with the Declaration of Helsinki and it was approved by the Ethics Committee of the University of Debrecen (approval code: HRB/052/00511-2; approved on 12.11.2013). Informed consent was obtained from the participating patients.

4.2. Laboratory Measurements

FXIII activity was determined by the ammonia release assay with blank correction [59] using TECHNOCHROM® reagent kit (Technoclone, Vienna, Austria) on Modular EVO P800 analyzer (Roche/Hitachi, Mannheim, Germany). The complex FXIII antigen (FXIII-A2B2) concentration was measured by ELISA [43]. Berichrom chromogenic antiplasmin test (Siemens, Marburg, Germany) was used for the determination of α2PI activity. Plasma fibrinogen concentration was measured by the Clauss method using the Labexpert LX fibrinogen assay kit (Labexpert Ltd., Debrecen, Hungary). High sensitivity CRP (HS) reagent from Diagnosticum Ltd. (Budapest, Hungary) was used for the measuring CRP concentration. Serum albumin concentration was measured by the bromocresol purple absorption method on Roche/Hitachi cobas c system.

4.3. Statistical Analysis

Statistical analysis of the results was performed by the Statistical Package for Social Science (SPSS, 22.0, Chicago, IL, USA) and by GraphPad Prism version 5.0 (GraphPad Software, Inc., San Diego, CA, USA). Distribution of the data was evaluated by the Kolmogorov Smirnov test. GraphPad Prism software was used for the construction of the figures. In case of nonparametric distribution, the results measured after HDF treatment and following the two-week HD treatment were compared by related-samples Wilcoxon signed rank test, while in case of parametric distributions related sample t-test was used. Differences in tested parameters measured before, one and four hours after the initiation of individual HDF and HD treatment were compared by Friedman test (nonparametric distribution) or by repeated measure ANOVA test (parametric distribution). The association between various parameters were analyzed by Spearman rank correlation.

5. Conclusions

In ESRD patients being on chronic HDF or HD treatment fibrinogen, FXIII antigen concentrations and FXIII activity were elevated, while α2PI activity decreased. As demonstrated by the significant correlation between the CRP level and fibrinogen concentration, the inflammatory status was a key determinant of fibrinogen concentration, but not of FXIII and α2PI levels. During a 4-h course of individual HDF or HD treatment, fibrinogen concentration and FXIII levels gradually elevated. However, when normalized for plasma albumin concentration, only the FXIII elevation remained significant. As opposed to fibrinogen and FXIII, the effect of individual HDF and HD treatments on plasma α2PI activity was different. After normalization to albumin significantly decreased α2PI activity was measured during HDF treatment. In HD treated patients, α2PI activities became elevated but the elevation disappeared after normalization. Elevated fibrinogen and FXIII levels in ESRD patients might contribute to the increased thrombosis risk, while decreased α2PI activity might be associated with elevated fibrinolytic potential.

Supplementary Materials

The following are available online at https://www.mdpi.com/1422-0067/21/22/8426/s1.

Author Contributions

Design of the study, K.P., J.B. and L.M.; determination of fibrinogen, C-reactive protein, FXIII antigen concentrations, measurement of FXIII and α2PI activities, B.H., K.P. and É.K.; collecting patient’s data and providing patient’s care, G.B. and J.B.; statistical calculations, K.P. and É.K.; construction of figures, K.P. and B.H.; writing and reviewing the manuscript, K.P., J.B. and L.M. All authors have read and agreed to the published version of the manuscript.

Funding

The research was funded by a grant from the National Research, Development and Innovation Office (NKFIH) (K129287), by the GINOP 2.3.2-15-2016-00050 project co-financed by the European Union and the European Regional Development Fund and by the Hungarian Academy of Science (11014 project).

Acknowledgments

The authors are indebted to Gizella Haramura (University of Debrecen, Debrecen, Hungary) for the expert technical assistance and to Fanni Puter (University of Debrecen, Debrecen, Hungary) for her help in constructing the Figures.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Abbreviations

α2PIα2-plasmin inhibitor
CRPC-reactive protein
ESRDend-stage renal disease
FXIIIblood coagulation factor XIII
FXIII-AFXIII A subunit
FXIII-BFXIII B subunit
HDhemodialysis
HDFhemodiafiltration
IQRinterquartile range

References

  1. Canaud, B.; Chenine, L.; Henriet, D.; Leray, H. Online hemodiafiltration: A multipurpose therapy for improving quality of renal replacement therapy. Contrib. Nephrol. 2008, 161, 191–198. [Google Scholar] [PubMed]
  2. Vanholder, R.; Meert, N.; Schepers, E.; Glorieux, G. From uremic toxin retention to removal by convection: Do we know enough? Contrib. Nephrol. 2008, 161, 125–131. [Google Scholar] [PubMed]
  3. Pavord, S.; Myers, B. Bleeding and thrombotic complications of kidney disease. Blood Rev. 2011, 25, 271–278. [Google Scholar] [CrossRef] [PubMed]
  4. Lutz, J.; Menke, J.; Sollinger, D.; Schinzel, H.; Thurmel, K. Haemostasis in chronic kidney disease. Nephrol. Dial. Transplant. 2014, 29, 29–40. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Becs, G.; Hudak, R.; Fejes, Z.; Debreceni, I.B.; Bhattoa, H.P.; Balla, J.; Kappelmayer, J. Haemodiafiltration elicits less platelet activation compared to haemodialysis. BMC Nephrol. 2016, 17, 147. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Gackler, A.; Rohn, H.; Lisman, T.; Benko, T.; Witzke, O.; Kribben, A.; Saner, F.H. Evaluation of hemostasis in patients with end-stage renal disease. PLoS ONE 2019, 14, e0212237. [Google Scholar] [CrossRef]
  7. Acedillo, R.R.; Shah, M.; Devereaux, P.J.; Li, L.; Iansavichus, A.V.; Walsh, M.; Garg, A.X. The risk of perioperative bleeding in patients with chronic kidney disease: A systematic review and meta-analysis. Ann. Surg. 2013, 258, 901–913. [Google Scholar] [CrossRef] [Green Version]
  8. Montagnana, M.; Meschi, T.; Borghi, L.; Lippi, G. Thrombosis and occlusion of vascular access in hemodialyzed patients. Semin. Thromb. Hemost. 2011, 37, 946–954. [Google Scholar] [CrossRef] [Green Version]
  9. Casserly, L.F.; Dember, L.M. Thrombosis in end-stage renal disease. Semin. Dial. 2003, 16, 245–256. [Google Scholar] [CrossRef]
  10. Ocak, G.; Vossen, C.Y.; Rotmans, J.I.; Lijfering, W.M.; Rosendaal, F.R.; Parlevliet, K.J.; Krediet, R.T.; Boeschoten, E.W.; Dekker, F.W.; Verduijn, M. Venous and arterial thrombosis in dialysis patients. Thromb. Haemost. 2011, 106, 1046–1052. [Google Scholar] [CrossRef] [Green Version]
  11. Lu, H.Y.; Liao, K.M. Increased risk of deep vein thrombosis in end-stage renal disease patients. BMC Nephrol. 2018, 19, 204. [Google Scholar] [CrossRef] [PubMed]
  12. Cheung, K.L.; Bouchard, B.A.; Cushman, M. Venous thromboembolism, factor VIII and chronic kidney disease. Thromb. Res. 2018, 170, 10–19. [Google Scholar] [CrossRef] [PubMed]
  13. Opatrny, K., Jr.; Zemanova, P.; Opatrna, S.; Vit, L. Fibrinolysis in chronic renal failure, dialysis and renal transplantation. Ann. Transplant. 2002, 7, 34–43. [Google Scholar] [PubMed]
  14. Hasuike, Y.; Kakita, N.; Aichi, M.; Masachika, S.; Kantou, M.; Ikeda Takahashi, S.; Nanami, M.; Nagasawa, Y.; Kuragano, T.; Nakanishi, T. Imbalance of coagulation and fibrinolysis can predict vascular access failure in patients on hemodialysis after vascular access intervention. J. Vasc. Surg. 2019, 69, 174–180. [Google Scholar] [CrossRef]
  15. Nelson, K.; Thethi, I.; Cunanan, J.; Hoppensteadt, D.; Bajwa, R.; Fareed, J.; Bansal, V. Upregulation of surrogate markers of inflammation and thrombogenesis in patients with ESRD: Pathophysiologic and therapeutic implications. Clin. Appl. Thromb. Hemost. 2011, 17, 302–304. [Google Scholar] [CrossRef]
  16. Molino, D.; De Santo, N.G.; Marotta, R.; Anastasio, P.; Mosavat, M.; De Lucia, D. Plasma levels of plasminogen activator inhibitor type 1, factor VIII, prothrombin activation fragment 1 + 2, anticardiolipin, and antiprothrombin antibodies are risk factors for thrombosis in hemodialysis patients. Semin. Nephrol. 2004, 24, 495–501. [Google Scholar] [CrossRef]
  17. Winter, W.E.; Greene, D.N.; Beal, S.G.; Isom, J.A.; Manning, H.; Wilkerson, G.; Harris, N. Clotting factors: Clinical biochemistry and their roles as plasma enzymes. Adv. Clin. Chem. 2020, 94, 31–84. [Google Scholar]
  18. Vilar, R.; Fish, R.J.; Casini, A.; Neerman-Arbez, M. Fibrin(ogen) in human disease: Both friend and foe. Haematologica 2020, 105, 284–296. [Google Scholar] [CrossRef] [Green Version]
  19. de Vries, J.J.; Snoek, C.J.M.; Rijken, D.C.; de Maat, M.P.M. Effects of Post-Translational Modifications of Fibrinogen on Clot Formation, Clot Structure, and Fibrinolysis: A Systematic Review. Arterioscler. Thromb. Vasc. Biol. 2020, 40, 554–569. [Google Scholar] [CrossRef]
  20. Muszbek, L.; Bereczky, Z.; Bagoly, Z.; Komaromi, I.; Katona, E. Factor XIII: A coagulation factor with multiple plasmatic and cellular functions. Physiol. Rev. 2011, 91, 931–972. [Google Scholar] [CrossRef] [Green Version]
  21. Bagoly, Z.; Koncz, Z.; Harsfalvi, J.; Muszbek, L. Factor XIII, clot structure, thrombosis. Thromb. Res. 2012, 129, 382–387. [Google Scholar] [CrossRef] [PubMed]
  22. Urano, T.; Suzuki, Y.; Iwaki, T.; Sano, H.; Honkura, N.; Castellino, F.J. Recognition of Plasminogen Activator Inhibitor Type 1 as the Primary Regulator of Fibrinolysis. Curr. Drug Targets 2019, 20, 1695–1701. [Google Scholar] [CrossRef] [PubMed]
  23. Carmassi, F.; Mariani, G.; Palla, R.; Fusani, L.; Bionda, A.; Molea, N.; Bianchi, R. Coagulation factor XIII in patients with acute and chronic renal disease. Nephron 1980, 25, 179–183. [Google Scholar] [CrossRef] [PubMed]
  24. Vaziri, N.D.; Gonzales, E.C.; Wang, J.; Said, S. Blood coagulation, fibrinolytic, and inhibitory proteins in end-stage renal disease: Effect of hemodialysis. Am. J. Kidney Dis. 1994, 23, 828–835. [Google Scholar] [CrossRef]
  25. Kolb, G.; Fischer, W.; Seitz, R.; Muller, T.; Egbring, R.; Lange, H.; Havemann, K. Hemodialysis and blood coagulation: The effect of hemodialysis on coagulation factor XIII and thrombin-antithrombin III complex. Nephron 1991, 58, 106–108. [Google Scholar] [CrossRef] [PubMed]
  26. Erdem, Y.; Haznedaroglu, I.C.; Celik, I.; Yalcin, A.U.; Yasavul, U.; Turgan, C.; Caglar, S. Coagulation, fibrinolysis and fibrinolysis inhibitors in haemodialysis patients: Contribution of arteriovenous fistula. Nephrol. Dial. Transplant. 1996, 11, 1299–1305. [Google Scholar] [CrossRef]
  27. Prinsen, B.H.; Rabelink, T.J.; Beutler, J.J.; Kaysen, G.A.; De Boer, J.; Boer, W.H.; Hagen, E.C.; Berger, R.; De Sain-Van Der Velden, M.G. Increased albumin and fibrinogen synthesis rate in patients with chronic renal failure. Kidney Int. 2003, 64, 1495–1504. [Google Scholar] [CrossRef] [Green Version]
  28. Zoccali, C.; Mallamaci, F.; Tripepi, G.; Cutrupi, S.; Parlongo, S.; Malatino, L.S.; Bonanno, G.; Rapisarda, F.; Fatuzzo, P.; Seminara, G.; et al. Fibrinogen, mortality and incident cardiovascular complications in end-stage renal failure. J. Intern. Med. 2003, 254, 132–139. [Google Scholar] [CrossRef]
  29. Kaysen, G.A.; Dubin, J.A.; Muller, H.G.; Mitch, W.E.; Rosales, L.; Levin, N.W.; Group, H. 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. [Google Scholar] [CrossRef] [Green Version]
  30. Fish, R.J.; Neerman-Arbez, M. Fibrinogen gene regulation. Thromb. Haemost. 2012, 108, 419–426. [Google Scholar] [CrossRef]
  31. Danesh, J.; Collins, R.; Appleby, P.; Peto, R. Association of fibrinogen, C-reactive protein, albumin, or leukocyte count with coronary heart disease: Meta-analyses of prospective studies. JAMA 1998, 279, 1477–1482. [Google Scholar] [CrossRef]
  32. Aydin, S.; Ugur, K.; Aydin, S.; Sahin, I.; Yardim, M. Biomarkers in acute myocardial infarction: Current perspectives. Vasc. Health Risk Manag. 2019, 15, 1–10. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Fibrinogen Studies, C.; Danesh, J.; Lewington, S.; Thompson, S.G.; Lowe, G.D.; Collins, R.; Kostis, J.B.; Wilson, A.C.; Folsom, A.R.; Wu, K.; et al. Plasma fibrinogen level and the risk of major cardiovascular diseases and nonvascular mortality: An individual participant meta-analysis. JAMA 2005, 294, 1799–1809. [Google Scholar]
  34. de Lau, L.M.; Leebeek, F.W.; de Maat, M.P.; Koudstaal, P.J.; Dippel, D.W. A review of hereditary and acquired coagulation disorders in the aetiology of ischaemic stroke. Int. J. Stroke 2010, 5, 385–394. [Google Scholar] [CrossRef] [PubMed]
  35. Nishimoto, K.; Yamagami, S.; Katoh, Y.; Kishimoto, T.; Maekawa, M.; Okada, K.; Matsuo, O. Coagulation and fibrinolysis in chronic renal failure. Change in tissue-type plasminogen activator activity. ASAIO Trans. 1986, 32, 478–481. [Google Scholar] [CrossRef]
  36. Kirmizis, D.; Tsiandoulas, A.; Pangalou, M.; Koutoupa, E.; Rozi, P.; Protopappa, M.; Barboutis, K. Validity of plasma fibrinogen, D-dimer, and the von Willebrand factor as markers of cardiovascular morbidity in patients on chronic hemodialysis. Med. Sci. Monit. 2006, 12, CR55–CR62. [Google Scholar] [CrossRef]
  37. Raj, D.S.; Dominic, E.A.; Wolfe, R.; Shah, V.O.; Bankhurst, A.; Zager, P.G.; Ferrando, A. Coordinated increase in albumin, fibrinogen, and muscle protein synthesis during hemodialysis: Role of cytokines. Am. J. Physiol. Endocrinol. Metab. 2004, 286, E658–E664. [Google Scholar] [CrossRef] [Green Version]
  38. Sabovic, M.; Salobir, B.; Preloznik Zupan, I.; Bratina, P.; Bojec, V.; Buturovic Ponikvar, J. The influence of the haemodialysis procedure on platelets, coagulation and fibrinolysis. Pathophysiol. Haemost. Thromb. 2005, 34, 274–278. [Google Scholar] [CrossRef]
  39. Derosa, G.; Libetta, C.; Esposito, P.; Borettaz, I.; Tinelli, C.; D’Angelo, A.; Maffioli, P. Effects of two different dialytic treatments on inflammatory markers in people with end-stage renal disease with and without type 2 diabetes mellitus. Cytokine 2017, 92, 75–79. [Google Scholar] [CrossRef]
  40. Khatib-Massalha, E.; Michelis, R.; Trabelcy, B.; Gerchman, Y.; Kristal, B.; Ariel, A.; Sela, S. Free circulating active elastase contributes to chronic inflammation in patients on hemodialysis. Am. J. Physiol. Renal. Physiol. 2018, 314, F203–F209. [Google Scholar] [CrossRef]
  41. Bagoly, Z.; Fazakas, F.; Komaromi, I.; Haramura, G.; Toth, E.; Muszbek, L. Cleavage of factor XIII by human neutrophil elastase results in a novel active truncated form of factor XIII A subunit. Thromb. Haemost. 2008, 99, 668–674. [Google Scholar] [CrossRef] [PubMed]
  42. Beckers, C.M.L.; Simpson, K.R.; Griffin, K.J.; Brown, J.M.; Cheah, L.T.; Smith, K.A.; Vacher, J.; Cordell, P.A.; Kearney, M.T.; Grant, P.J.; et al. Cre/lox Studies Identify Resident Macrophages as the Major Source of Circulating Coagulation Factor XIII-A. Arterioscler. Thromb. Vasc. Biol. 2017, 37, 1494–1502. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Katona, E.; Haramura, G.; Karpati, L.; Fachet, J.; Muszbek, L. A simple, quick one-step ELISA assay for the determination of complex plasma factor XIII (A2B2). Thromb. Haemost. 2000, 83, 268–273. [Google Scholar] [CrossRef] [PubMed]
  44. Greenberg, C.S.; Shuman, M.A. The zymogen forms of blood coagulation factor XIII bind specifically to fibrinogen. J. Biol. Chem. 1982, 257, 6096–6101. [Google Scholar]
  45. Siebenlist, K.R.; Meh, D.A.; Mosesson, M.W. Plasma factor XIII binds specifically to fibrinogen molecules containing gamma chains. Biochemistry 1996, 35, 10448–10453. [Google Scholar] [CrossRef] [PubMed]
  46. Aleman, M.M.; Byrnes, J.R.; Wang, J.G.; Tran, R.; Lam, W.A.; Di Paola, J.; Mackman, N.; Degen, J.L.; Flick, M.J.; Wolberg, A.S. Factor XIII activity mediates red blood cell retention in venous thrombi. J. Clin. Investig. 2014, 124, 3590–3600. [Google Scholar] [CrossRef] [Green Version]
  47. Mezei, Z.A.; Katona, E.; Kallai, J.; Bereczky, Z.; Molnar, E.; Kovacs, B.; Ajzner, E.; Bagoly, Z.; Miklos, T.; Muszbek, L. Regulation of plasma factor XIII levels in healthy individuals; a major impact by subunit B intron K, c. 1952 + 144 C > G polymorphism. Thromb. Res. 2016, 148, 101–106. [Google Scholar] [CrossRef]
  48. Bereczky, Z.; Balogh, E.; Katona, E.; Czuriga, I.; Edes, I.; Muszbek, L. Elevated factor XIII level and the risk of myocardial infarction in women. Haematologica 2007, 92, 287–288. [Google Scholar] [CrossRef] [Green Version]
  49. Shemirani, A.H.; Szomjak, E.; Csiki, Z.; Katona, E.; Bereczky, Z.; Muszbek, L. Elevated factor XIII level and the risk of peripheral artery disease. Haematologica 2008, 93, 1430–1432. [Google Scholar] [CrossRef] [Green Version]
  50. Balogh, L.; Katona, E.; Mezei, Z.A.; Kallai, J.; Gindele, R.; Edes, I.; Muszbek, L.; Papp, Z.; Bereczky, Z. Effect of factor XIII levels and polymorphisms on the risk of myocardial infarction in young patients. Mol. Cell Biochem. 2018, 448, 199–209. [Google Scholar] [CrossRef]
  51. Mezei, Z.A.; Katona, E.; Kallai, J.; Bereczky, Z.; Somodi, L.; Molnar, E.; Kovacs, B.; Miklos, T.; Ajzner, E.; Muszbek, L. Factor XIII levels and factor XIII B subunit polymorphisms in patients with venous thromboembolism. Thromb. Res. 2017, 158, 93–97. [Google Scholar] [CrossRef] [PubMed]
  52. Reed, G.L.; Houng, A.K.; Singh, S.; Wang, D. alpha2-Antiplasmin: New Insights and Opportunities for Ischemic Stroke. Semin. Thromb. Hemost. 2017, 43, 191–199. [Google Scholar] [PubMed] [Green Version]
  53. Jain, S.; Acharya, S.S. Inherited disorders of the fibrinolytic pathway. Transfus. Apher. Sci. 2019, 58, 572–577. [Google Scholar] [CrossRef] [PubMed]
  54. Meltzer, M.E.; Doggen, C.J.; de Groot, P.G.; Rosendaal, F.R.; Lisman, T. Plasma levels of fibrinolytic proteins and the risk of myocardial infarction in men. Blood 2010, 116, 529–536. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Suri, M.F.; Yamagishi, K.; Aleksic, N.; Hannan, P.J.; Folsom, A.R. Novel hemostatic factor levels and risk of ischemic stroke: The Atherosclerosis Risk in Communities (ARIC) Study. Cerebrovasc. Dis. 2010, 29, 497–502. [Google Scholar] [CrossRef] [Green Version]
  56. Reed, G.L.; Houng, A.K.; Wang, D. Microvascular thrombosis, fibrinolysis, ischemic injury, and death after cerebral thromboembolism are affected by levels of circulating alpha2-antiplasmin. Arterioscler. Thromb. Vasc. Biol. 2014, 34, 2586–2593. [Google Scholar] [CrossRef] [Green Version]
  57. Matsuno, H.; Okada, K.; Ueshima, S.; Matsuo, O.; Kozawa, O. Alpha2-antiplasmin plays a significant role in acute pulmonary embolism. J. Thromb. Haemost. 2003, 1, 1734–1739. [Google Scholar] [CrossRef]
  58. Nakamura, Y.; Chida, Y.; Tomura, S. Enhanced coagulation-fibrinolysis in patients on regular hemodialysis treatment. Nephron 1991, 58, 201–204. [Google Scholar] [CrossRef]
  59. Karpati, L.; Penke, B.; Katona, E.; Balogh, I.; Vamosi, G.; Muszbek, L. A modified, optimized kinetic photometric assay for the determination of blood coagulation factor XIII activity in plasma. Clin. Chem. 2000, 46, 1946–1955. [Google Scholar] [CrossRef]
Ijms 21 08426 g001 550
Figure 1. Fibrinogen concentration, C-reactive protein (CRP) level and their relationship in patients with end-stage renal disease. (A) Fibrinogen concentration and (B) CRP level in patients being on permanent HDF treatment and after switching to HD treatment for two weeks. Longer horizontal lines demonstrate median values (numerical values are also shown), shorter horizontal lines depict the upper and lower limits of interquartile range. The four outliers with CRP level higher than 50 mg/L in the HDF group are labelled by asterisk in both (A,B). (C,D) demonstrate the relationship between CRP level and fibrinogen concentration in HDF treated patients and after HD treatment, respectively. CRP: C-reactive protein, HDF: hemodiafiltration, HD hemodialysis, ns: not significant, r2: coefficients of determination.
Figure 1. Fibrinogen concentration, C-reactive protein (CRP) level and their relationship in patients with end-stage renal disease. (A) Fibrinogen concentration and (B) CRP level in patients being on permanent HDF treatment and after switching to HD treatment for two weeks. Longer horizontal lines demonstrate median values (numerical values are also shown), shorter horizontal lines depict the upper and lower limits of interquartile range. The four outliers with CRP level higher than 50 mg/L in the HDF group are labelled by asterisk in both (A,B). (C,D) demonstrate the relationship between CRP level and fibrinogen concentration in HDF treated patients and after HD treatment, respectively. CRP: C-reactive protein, HDF: hemodiafiltration, HD hemodialysis, ns: not significant, r2: coefficients of determination.
Ijms 21 08426 g001
Ijms 21 08426 g002 550
Figure 2. FXIII levels in the plasma of ESRD patients. Plasma FXIII activity (A) and antigen concentration (B) of patients being on chronic HDF treatment or after two weeks of HD treatment. (C) and (D) correlation of the results obtained by activity measurement and immuno-assay; (E,F) correlation of FXIII levels with the age of ESRD patients. HDF: hemodiafiltration, HD hemodialysis, ns: not significant, r2: coefficients of determination. The asterisks on (A,B) represent the four patients with the highest CRP levels.
Figure 2. FXIII levels in the plasma of ESRD patients. Plasma FXIII activity (A) and antigen concentration (B) of patients being on chronic HDF treatment or after two weeks of HD treatment. (C) and (D) correlation of the results obtained by activity measurement and immuno-assay; (E,F) correlation of FXIII levels with the age of ESRD patients. HDF: hemodiafiltration, HD hemodialysis, ns: not significant, r2: coefficients of determination. The asterisks on (A,B) represent the four patients with the highest CRP levels.
Ijms 21 08426 g002
Ijms 21 08426 g003 550
Figure 3. α2-plasmin inhibitor activity in ESRD patients. (A) patients being on chronic HDF treatment or after switching to HD treatment for two weeks. (B) correlation of α2-plasmin inhibitor activity with patients’ age. The coefficient of determination (r2) is also shown in the figure. The asterisks on Figure A represent the four patients with the highest CRP levels.
Figure 3. α2-plasmin inhibitor activity in ESRD patients. (A) patients being on chronic HDF treatment or after switching to HD treatment for two weeks. (B) correlation of α2-plasmin inhibitor activity with patients’ age. The coefficient of determination (r2) is also shown in the figure. The asterisks on Figure A represent the four patients with the highest CRP levels.
Ijms 21 08426 g003
Ijms 21 08426 g004 550
Figure 4. Changes of plasma fibrinogen concentration in ESRD patients during a 4-h HDF (A,C) or HD (B,D) treatment. The two upper figures demonstrate fibrinogen concentrations not corrected for albumin (A,B), while the two lower figures show fibrinogen concentrations corrected for albumin (C,D). Long and short horizontal lines in the figures represent median values and limits of interquartile ranges, respectively. Significant differences between results obtained before and after treatments are indicated by the p values above thin horizontal lines.
Figure 4. Changes of plasma fibrinogen concentration in ESRD patients during a 4-h HDF (A,C) or HD (B,D) treatment. The two upper figures demonstrate fibrinogen concentrations not corrected for albumin (A,B), while the two lower figures show fibrinogen concentrations corrected for albumin (C,D). Long and short horizontal lines in the figures represent median values and limits of interquartile ranges, respectively. Significant differences between results obtained before and after treatments are indicated by the p values above thin horizontal lines.
Ijms 21 08426 g004
Ijms 21 08426 g005 550
Figure 5. Changes of plasma FXIII activity in ESRD patients during a 4-h HDF (A,C) or HD (B,D) treatment. The upper two figures show FXIII activities not corrected for albumin (A,B), while FXIII activities corrected for albumin concentration are shown in the two lower figures (C,D). Horizontal lines represent mean FXIII activities. Significant differences between results obtained before and after treatments are indicated by the p values above thin horizontal lines.
Figure 5. Changes of plasma FXIII activity in ESRD patients during a 4-h HDF (A,C) or HD (B,D) treatment. The upper two figures show FXIII activities not corrected for albumin (A,B), while FXIII activities corrected for albumin concentration are shown in the two lower figures (C,D). Horizontal lines represent mean FXIII activities. Significant differences between results obtained before and after treatments are indicated by the p values above thin horizontal lines.
Ijms 21 08426 g005
Ijms 21 08426 g006 550
Figure 6. Changes of plasma α2PI activity in ESRD patients during a 4-h HDF (A,C) or HD (B,D) treatment. The upper two figures show α2PI activities not corrected for albumin (A,B), while α2PI activities corrected for albumin concentration are shown in the two lower figures (C,D). The horizontal lines represent mean activities. Significant differences between results obtained before and after treatments are indicated by the p values above thin horizontal lines.
Figure 6. Changes of plasma α2PI activity in ESRD patients during a 4-h HDF (A,C) or HD (B,D) treatment. The upper two figures show α2PI activities not corrected for albumin (A,B), while α2PI activities corrected for albumin concentration are shown in the two lower figures (C,D). The horizontal lines represent mean activities. Significant differences between results obtained before and after treatments are indicated by the p values above thin horizontal lines.
Ijms 21 08426 g006
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Pénzes, K.; Hurják, B.; Katona, É.; Becs, G.; Balla, J.; Muszbek, L. Terminal Phase Components of the Clotting Cascade in Patients with End-Stage Renal Disease Undergoing Hemodiafiltration or Hemodialysis Treatment. Int. J. Mol. Sci. 2020, 21, 8426. https://doi.org/10.3390/ijms21228426

AMA Style

Pénzes K, Hurják B, Katona É, Becs G, Balla J, Muszbek L. Terminal Phase Components of the Clotting Cascade in Patients with End-Stage Renal Disease Undergoing Hemodiafiltration or Hemodialysis Treatment. International Journal of Molecular Sciences. 2020; 21(22):8426. https://doi.org/10.3390/ijms21228426

Chicago/Turabian Style

Pénzes, Krisztina, Boglárka Hurják, Éva Katona, Gergely Becs, József Balla, and László Muszbek. 2020. "Terminal Phase Components of the Clotting Cascade in Patients with End-Stage Renal Disease Undergoing Hemodiafiltration or Hemodialysis Treatment" International Journal of Molecular Sciences 21, no. 22: 8426. https://doi.org/10.3390/ijms21228426

APA Style

Pénzes, K., Hurják, B., Katona, É., Becs, G., Balla, J., & Muszbek, L. (2020). Terminal Phase Components of the Clotting Cascade in Patients with End-Stage Renal Disease Undergoing Hemodiafiltration or Hemodialysis Treatment. International Journal of Molecular Sciences, 21(22), 8426. https://doi.org/10.3390/ijms21228426

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop