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Journal of Clinical Medicine Research

Original Article

Volume 10, Number 9, September 2018, pages 700-706

Soluble Fms-Like Tyrosine Kinase-1 Is A Marker of Endothelial Dysfunction During Sepsis

Vascular endothelial cells are critically involved in the pathogenesis of sepsis-induced organ failure given their participation in coagulation, increased permeability, vasodilatation, vascular barrier and leukocytes activation and trafficking. Because of their ubiquitous distribution throughout all vascular beds, endothelial cells participate in early and delayed inflammatory responses in sepsis [1, 2]. During the early phases of sepsis, endothelial cells are directly activated by microbial factors such as lipopolysaccharide (LPS) and bacterial lipoproteins in a permeable, pro-inflammatory and pro-thrombotic phenotype. The activated endothelium is critical for vascular remodeling and repair, leukocytes trafficking and eradication of pathogens.

Subsequently, endogenous inflammatory agonists released by activated leukocytes and endothelial cells further promote endothelial dysfunction, either on their own or in synergy with circulating microbial molecules (pro-inflammatory cytokines promote self-reinforcing increase of innate immune cells, adhesion molecules and chemokines expression, induction of complement and fibrinogen, determine NEToses [3], cause release of inflammatory microparticles [4], up-regulate tissue factor expression by blood monocytes and immuno-thrombosis [5], disseminated intravascular coagulation results in impaired microvascular function and organ injury [6]).

When the response exceeds a certain threshold, systemic injury occurs, and the endothelial response becomes detrimental, uncontrolled, persistent and widespread.

Many circulating biomarkers have been proposed in literature (see [7] for review), including mediators of vasomotor tone and permeability (as VEGF, sFlt-1).

VEGF is a key regulator of angiogenesis, promoting endothelial cell survival, growth and migration [8]. However, it also plays a crucial role in the disruption of endothelium during inflammation, promoting vasodilatation and permeability.

Under quiescence condition VEGF signaling plays a critical role in homeostasis. VEGF binds to two Fms-like tyrosine kinase receptors on endothelial cells, VEGFR1 or Flt-1 and VEGFR2 or Flk-1. During activated state (sepsis), circulating levels of VEGF are increased. Elevated VEGF signaling, in turn, leads to increased vascular leak, leukocyte adhesion/trafficking and clot formation. VEGF binds also to a soluble form of the receptor of VEGF (soluble VEGFR1 or sFlt-1). This soluble variant is a truncated protein lacking the tyrosine-kinase domain responsible of intracellular signal transduction, thus acting as a competitive inhibitor of VEGF signaling in endothelial cells. Sepsis-mediated induction of sFlt-1 may represent a critical component of the host anti-inflammatory response. Previous studies have investigated VEGF and sFlt-1 involvement in sepsis and disease severity [9-17] yielding conflicting results if the degree of elevation correlates with the state of disease. sFLT-1 has been recently suggested as a marker for abnormal vascular remodeling state, e.g., preeclampsia [18].

In the present study, we investigated correlation of sFlt-1 levels in sepsis, possibly as a marker of endothelial dysfunction and its correlation with sepsis-related sequential organ failure assessment (SOFA) score including in a group of patients after sepsis resolution.

The present study has been conducted on 170 consecutive patients hospitalized in different medical and surgical wards of the Vito Fazzi Hospital of Lecce (Italy) for whom blood culture was requested based on different clinical suspicions, and in 18 (not hospitalized) healthy volunteers. Informed written consent was obtained from all patients or, if unobtainable, their relatives’ consent was attained as designed by ethic committee. For a subgroup of 9 individuals, serum sample was obtained also after negativization of blood culture.

Serum levels of sFlt-1 were determined by fully automated ElectroChemiLuminescence Immuno Asssay (ECLIA) on the immunoanalyzer Elecsys 2010®, Modular Analytics E170, according to manufacturer recommendations (Roche Diagnostic GmbH) and expressed in pg/mL. All sera were collected at the time of blood culture and stored at -20 °C until sFlt-1 assay.

Blood cultures were performed in patients with clinical symptoms of blood stream infections prior the administration of antimicrobial therapy. For each patient, at least two bottle sets were used for each septic episode; approximately 10 mL of blood was inoculated in the aerobic and anaerobic bottle (BACT/ALERT Culture Media, Biomerieux, Marcy-l’Etoile, France); the bottles were entered in the BACT/ALERT 3D System for the incubation and measure of the color change in response to shift in pH as a result of rising of CO₂ levels produced by microorganisms. In positive samples, bacteria and yeasts were identified on the Vitek 2 system (Biomerieux, Marcy-l’Etoile, France), according to manufacturer directions.

The SOFA score was used to quantify organ dysfunction. The SOFA score, a mortality prediction score, is based on the degree of dysfunction of six organ systems: respiration score is assessed by fraction of inspired oxygen and PaO₂, coagulation score by platelets count, liver score by total bilirubin, neurological by Glasgow Coma Scale, cardiovascular score by mean of arterial pressure and use of vasopressors, renal score by serum creatinine or urine output. To each organ, system is assigned a point value from 0 (normal) to 4 (high degree of dysfunction/failure). The SOFA score ranges from 0 to 24; higher value indicates greater organ failure and worst prognosis [19].

Data comparison was performed by Student’s t-test; statistical significance of difference between analyzed groups of patients was based on p value (< 0.05); Chi-squared test was used to evaluate significance of parameters associated to a clinical condition in different groups. Correlation trend was determined by Chi-squared test for trend. Statistical analyses were performed by MedCalc v18.1.2 statistical software.

The population of 170 hospitalized patients analyzed in the present study was subgrouped according to blood culture positivity and according to patient’s ward of provenience. We obtained 77 individuals with sepsis (as confirmed by a positive blood culture) and 93 negative, of which only 66 has been used as sepsis-negative controls, while a subgroup of 27 (of the 93 negatives: including 14 surgical patients and 13 new borns) was separately analyzed due to a potential endothelial modification after surgery or after birth, i.e., not baseline condition for sFlt-1 assay. In a small number of patients (nine individuals), s-Flt1 concentration was evaluated after negativization of the blood culture. Not hospitalized individuals (18 healthy volunteers) were used as negative controls (Table 1).

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Table 1. Patients Population and Percentages of Microganisms Identified in Blood Cultures

Serum level of s-Flt1 was significantly higher in septic patients than sepsis-negative patients with average values of 277.7 ± 52.7 and 133.4 ± 12.4 pg/mL, respectively, and P = 0.0088 (Table 2, Fig. 1). Both groups of patients had significantly higher concentration of sFlt-1 than healthy individuals (78.9 ± 2.5 pg/mL, P < 0.0001). However, healthy individuals fit in a different condition compared to hospitalized patients and for this reason, in our study we referred to sepsis-negative hospitalized patients as control group in order to be able to compare patients in similar clinical conditions, besides sepsis.

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Table 2. sFlt-1 Serum Levels Observed in the Analyzed Groups of Patients and Statistical Summary of Results

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Figure 1. Serum levels of sFlt-1 in patients groups. Septic patients showed significantly higher levels of sFlt-1 compared to sepsis-negative patients and healthy controls (P values indicated in figure; where not indicated, difference was not statistically significant). Two subgroups of sepsis-negative patients who underwent surgery or new borns were separately analyzed due to a potential not baseline condition for sFlt-1 assay after surgery or after birth; they showed a statistically significant difference with healthy controls but not with sepsis-positive nor -negative patients. Results are showed in semilogarithmic plot.

Among sepsis-positive patients, 68% were infected by Gram-negative bacteria, 27% by Gram-positive bacteria and 8% of patients had Candida positive blood culture (Table 1). Serum level of s-Flt1 (Fig. 2) showed a significant difference between Gram-negative (274.1 pg/mL) and Gram-positive (145.7 pg/mL) sepsis (P = 0.021). Patients with Candida infection showed an intermediate level of s-Flt1 (176.5 pg/mL) and no significant difference with Gram-negative and Gram-positive sepsis.

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Figure 2. Serum levels of sFlt-1 in Gram-negative, Gram-positive, Candida infections and in sepsis-negative individuals. Significant higher levels of sFlt-1 have been observed in Gram-negative infected patients compared to both Gram-positive and sepsis-negative patients (P values indicated in figure; where not indicated, difference was not statistically significant).

We separately analyzed sepsis-negative patients from surgery ward as well as new-born patients since they showed an unexpected higher average serum level of s-Flt1 and high inter-individual variability (Table 2, Fig. 1). We associated this finding to a potential endothelial modification after surgery or after birth and we excluded them from the group of sepsis-negative controls, although difference between the two subgroups was not statistically significant.

Sequential organ failure assessment was evaluated in 20 patients with sepsis whose serum levels of sFlt-1 were higher than 190 pg/mL (this limit was established considering sFlt-1 levels over the upper limit of the 95% confidence interval (CI) of median value calculated for sepsis patients, Table 2). We observed a positive linear trend between sFlt-1 and SOFA score (Fig. 3a), with significant Chi-squared test for trend (P < 0.0001). Moreover, patients who survived to sepsis have been differentiated from patients deceased in consequences of the sepsis, and we found that worst clinical condition which determined the death of the patients were associated with higher serum levels of sFlt-1 and SOFA score (Fig. 3b) compared to alive patients (P < 0.05 by Chi-squared test).

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Figure 3. sFlt-1 and sequential organ failure assessment in selected septic patients with serum levels of sFlt-1 higher than 190 pg/mL (see text for details). (a) sFlt-1 and SOFA score correlation, P < 0.0001 by Chi-squared test for trend. (b) serum levels of sFlt-1 mean values in patients deceased after sepsis and in alive individuals; SOFA score mean values are reported in the second axis. Higher serum levels of sFlt-1 and SOFA score are observed in deceased patients compared to survived (P < 0.05 by Chi-squared test). sFlt-1 values are showed in semilogarithmic plot.

Serum levels of sFlt-1 were measured in nine patients after negativization of blood culture and we found that reduction of sFlt-1 was about 37%. In Gram- negative infections, the percentage of decrease was more evident compared to Gram-positive infections. Klebsiella pneumoniae and Pseudomonas aeruginosa infections showed higher range of pre- and post-sepsis variation for serum level of sFlt-1 (Fig. 4).

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Figure 4. sFlt-1 after sepsis resolution. (a) Serum levels of sFlt-1 measured in nine patients during and after sepsis. (b) Percentage reduction of sFlt-1 after sepsis. AV: mean percentage reduction.

Functional status of the vascular endothelium is of key importance in the maintenance of vasomotor tone, leukocytes trafficking, permeability and hemostasis. In the presence of an infectious disease, endothelial activation/dysfunction can lead to a lesion in microcirculation which can potentially compromise the function of multiple organs. Activation and dysfunction of the endothelium is characterized by increased permeability, vasodilatation, recruitment of leucocytes and a shift to pro-coagulant state. Hence, infections compromise the function of heart, liver, gut, kidney, lung and brain leading to hypotension and myocardial dysfunction, microvascular leak, thrombocytopenia with or without disseminated intravascular coagulation, acute respiratory distress syndrome, acute kidney injury and brain injury. Biochemical markers and clinical parameters are currently used to assess organ dysfunction during sepsis and are used to define the SOFA score, whose changes from baseline are index of sepsis severity, according to the new consensus definitions of sepsis and related criteria [6, 19]. Multiple Candidate biomarkers of endothelial activation/dysfunction have been proposed for use in evaluating functional status of endothelium in infectious diseases. The present work was aimed to evaluate implication of sFlt-1, a known mediator of vascular tone and permeability, in sepsis. In this perspective, we compared septic patients to a population of not-infected critically ill patients in order to figure out whether the changes were specific to sepsis or broader markers of illness state. First, we found a statistically significant difference in serum level of sFlt-1 between the two groups of patients (Fig. 1), and, as expected, both groups showed significant difference with the healthy control group of not hospitalized individuals. At the same time, we excluded from the no-sepsis control group patients with plausible vascular alteration and not stable conditions such as patients after surgery as well as the newborns. Average and median values of sFlt-1 measured in infected patients (277.7 and 165.5 pg/mL, respectively, Table 2) were similar to those previously reported [9-17]. Gram-negative infected individuals (68%, Table 1) showed higher values of serum sFlt-1 than patients with Gram-positive infections (Fig. 2). As previously published, LPS from Gram-negative bacteria membrane stimulates the macrophages inflammatory response by activation of Toll-like receptor 4 (TLR4), a LPS receptor on the cytoplasmic membrane. This has been proposed to orchestrate immune responses during gram-negative bacterial infection and to be associated to septic shock by excessive LPS challenge [20, 21].

Several markers of endothelial cell activation have been associated to sequential organ failure in septic patients, including sFlt-1 [22] and angiopoietin/Tie-2 axis as potential marker of sepsis diagnosis and outcome [6, 23-26], although no biomarker has achieved a uniform reproducibility across patients’ population and capacity to identify patients at high risk for complications or mortality, and none of them respond to criteria for ideal biomarker [7]. In the present study, we found a statistically significant positive trend of correlation (P < 0.0001) between the increased levels of sFlt-1 (mean: 528.8 pg/mL, in selected 23 patients with serum level over the upper limit of median 95% CI) and sequential organ failure evaluated according to the SOFA score (average: 8). Moreover, sFlt-1 and SOFA score were significantly higher in not-survivor individuals (8 of 20) than survivors (P < 0.05 by Chi-squared test). After resolution of sepsis and negativization of blood culture, we found an average 37% decrease of serum levels of sFlt-1; the highest variation of pre- and post-sepsis was due to Gram-negative infection (i.e., Klebsiella pneumoniae and Pseudomonas aeruginosa). We did not find any marked decrease in sFlt-1 concentration in no-sepsis control when the assay was repeated after a time interval similar to that of blood culture negativization. On the basis of our results, changes in sFlt-1 serum levels appear associated to the endothelial dysfunction of septic patients. The biological mechanism by which sFlt-1 is involved in regulating pathophysiology of sepsis is, so far, not completely understood. In this process, it is known that the sFlt-1 ligand, VEGF, is an important mediator of endothelial activation by intracellular signaling for the release of cytokines and chemokines, for the expression of procoagulant molecule, the increase of permeability and induction of cell adhesion molecules. However, the soluble receptor, sFlt-1, acts differently than membrane-bound receptors because it does not bring the VEGF signal inside the cell, competing with membrane bound Flt-1 for binding VEGF and thus acting as a decoy molecule. It has been proposed that sFlt-1 could contribute to the systemic anti-inflammatory host response to infection [27]. Our data showed a compensatory elevation of sFlt-1 level in serum of infected patients. The question of whether several fold higher elevation of sFlt-1 could effectively block the endothelial barrier disruption during sepsis is an exciting open question that remains to be answered.

In conclusion, although the limitation due to the small size of studied population, our results highlight the association of endothelial damage with the presence of the infection and the possibility to use serum levels of sFlt-1 as a maker of it. Further studies in a broader population as well as a larger correlation with organ failure assessment and LPS involvement to predict worst outcomes of the patients are ongoing to support present results.

Conflict of Interest

All authors declare no conflict of interest with any financial organization regarding the items discussed in the manuscript.

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Journal of Clinical Medicine Research is published by Elmer Press Inc.