Background
In December 2019, a novel Coronavirus, with person-to-person transmission emerged as a human pathogen [
1]. Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), causes coronavirus disease 2019 (COVID-19), which has a range of manifestations from asymptomatic to critical illness. SARS-CoV-2 affects mostly the respiratory system, causing viral pneumonitis that may lead to severe acute respiratory distress syndrome (ARDS) [
2,
3], however, disease course may result in multi-organ involvement, inducing renal dysfunction, myocardial injury, and hemodynamic instability [
4‐
6].
Early observations revealed a hypercoagulable state in COVID-19 patients, accompanied by elevated D-dimer and fibrinogen levels [
3,
7,
8]. These findings correlated with a higher rate of intensive care admissions, as well as mortality [
2,
6,
7,
9]. The rate of thrombotic complications appears to be higher amongst COVID-19 patients compared with other critically ill patients. Venous thromboembolic events (VTE) were found in 27 %- 69 % of these severe patients [
10,
11]. Of the patients with VTE, deep vein thrombosis (DVT) was reported with an incidence of 23 % [
12] (12.7 % in other non COVID-19 ICU patients [
13]), and pulmonary embolism (PE) with an unusually high incidence of up to 81 % in some series. [
10].
The mechanism underlying COVID-19 coagulopathy has yet to be fully elucidated, in order to obtain better control of this severe manifestation. High levels of FVIII were found in the plasma of COVID-19 patients [
14], and vWF levels were higher in the plasma of ICU hospitalized compared with non-severe COVID-19 patients [
15]. Reports have linked the hypercoagulable state with a hyperinflammatory state, as it appears that higher fibrinogen level were associated with higher IL-6 and CRP levels [
16,
17]. Inflammatory cytokines are established modulators of coagulation and fibrinolysis activation [
18]. The concept of immune thrombosis was coined, as cytokines were found to change the normal anticoagulant and profibrinolytic properties of the endothelium to an activated state [
19], induce tissue factor (TF) gene expression in endothelial cells and monocytes, fibrinogen synthesis, and platelet production [
20]. Autopsy findings indicated diffuse alveolar damage, coupled with microvascular involvement with intra- and extravascular fibrin deposition, and the frequent formation of microthombi in lung arterioles of COVID-19 patients [
21]. Lung tissues autopsies of 33/38 (83 %) COVID-19 patients reveled platelet-fibrin thrombi [
22]. Hence, fibrin deposition in damaged lung tissues is a prominent pathological aspect of the disease [
21‐
23]. Coagulation factor FXIII plays a central role in the stabilization of the fibrin-based clot, and may also support platelet adhesion at sites of vascular damage [
24]. Due to the significant presentations of fibrin deposition and platelets-fibrin microthrombi in the lungs of COVID-19 patients, we studied the levels of FXIII activity in the plasma of 34 severe COVID-19 patients. To the best of our knowledge this is a first report of low levels of FXIII in the plasma of severe COVID-19 patients. Possible mechanisms of FXIII deficiency involvement in COVID-19 morbidity are discussed.
Materials and methods
Patients and clinical assessment
This retrospective study was approved by the Tel Aviv Sourasky Medical Center local IRB. Consecutive COVID-19 patients, hospitalized in the ICU at the Tel Aviv Medical Center between March 10th 2020 and April 26th 2020 (7 patients, first outbreak in Israel), and January 5th to February 4th 2021 (27 patients, second outbreak in Israel) were included in the study. All patients were diagnosed with COVID-19, having a positive reverse-transcriptase–polymerase chain reaction assay for SARS-CoV-2 in a respiratory tract sample either prior to, or at admission. All patients were admitted to the ICU due to respiratory failure requiring ventilatory support (mechanical ventilation or high flow oxygen therapy). Demographic and clinical data of participating patients were obtained from the electronic medical records of each subject; these included: Age, gender, comorbid conditions, medications, laboratory findings, daily score of disease severity, invasive and noninvasive mechanical ventilation status, use of extracorporeal membrane oxygenation (ECMO), administration of hemodynamic support, acute cardiac injury, acute kidney injury, major bleeding events, thrombotic events and COVID-19 -related mortality. During their hospitalization, all patients underwent a comprehensive transthoracic echocardiography within 24 h of admission, being part of the routine baseline clinical assessment in ICU. Patients who then experienced clinical deterioration, determined as the need for intubation and mechanical ventilation, deterioration to severe level of hypoxemia (PaO2/FiO2<100), or new onset of circulatory shock, underwent repeated echocardiographic assessment as well as compression ultrasonography of femoral and popliteal veins of both legs.
Clinical definitions
Severe COVID-19 infection (WHO definition): SatO2<93 on ambient air, RR>30, PF<300.
PE: Lacking a CTA, a diagnosis of PE was based on the combination of acute deterioration in hypoxemia severity without significant change in respiratory resistance or compliance, and the presence of echocardiographic signs suggestive of acute right ventricular strain due to elevated pulmonary vascular resistance (McConell sign, RV dilatation and dysfunction).
Laboratory assays
3.5 ml of whole blood was collected into vacuum tubes (Greiner, Kremsmunster, Austria) containing 1/10 volume of 3.2 % trisodium citrate. The samples were centrifuged for 8 min at room temperature at 2,500 g, and the plasma was utilized for analysis within two hours. Prothrombin Time assay was performed utilizing Innovin as a recombinant human tissue factor (Dade, Siemens, Marburg, Germany), and measured in seconds. Activated Partial Thrombin Time assay was performed utilizing FSL actin (Dade, Siemens, Marburg, Germany), and measured in seconds. All these assays were performed on either CS2100i or CS5100 instruments (Sysmex, Kobe, Japan). Factor VIII activity was measured by the one-stage clotting assay based on APTT and factor VIII-deficient plasma (Siemens) on a CS2500 instrument (Sysmex). FXIII activity was measured by a FXIII kit (Berichrom, Siemens, Marburg, Germany) on a CS2100i instrument (Sysmex). FXIII-A antigen levels were measured by the commercial automated latex enhanced immunoassay (Werfan, MA, USA) according to the manufacturer’s instructions. Total neutrophils, monocytes and platelet counts were measured by Beckman coulter DxH800 CBC analyzers (Brea, CA, USA). All coagulation factor assays and CBC analyzers in the laboratory are subjected to the ECAT or CAP external quality control program, respectively, with excellent scores. The chemistry blood parameters: wide range CRP, alkaline phosphatase (ALP), Alanine Aminotransferase (ALT), Aspartate Aminotransferase (AST), Gamma-glutamyltransferase (GGT), Albumin and total bilirubin (TBIL) were measured by ADVIA system (Siemens Healthcare Diagnostics Inc., Tarrytown, NY 10591-5097 USA).
Statistics
Data collected included demographics, past medical history, clinical characteristics, and anticoagulation administered. Categorical variables are shown as frequencies and percentages, and continuous variables as means and standard deviations, or as medians and ranges in the cases of non-normal distributions of parameters. Student`s T-test was utilized to calculate statistical significance in continuous normal distributed variables, Mann Whitney for scale and continuous non-normal distributed variables and Chi square test for nominal variables, p<0.05 was considered significant. SPSS software (IBM SPSS Statistics for Windows, version 25, IBM corp., Armonk, NY, USA, 2017) was used for all statistical analyses.
Discussion
The high D-dimer levels and possibly systemic procoagulant state of COVID-19 patients prompted the postulation of a novel pulmonary intravascular coagulopathy [
25]. This theory is supported by autopsies performed on the lungs of COVID-19 patients, demonstrating small, firm thrombi and fibrin deposition in sections of the peripheral parenchyma in some of the cases [
21‐
23]. As previously shown, aberrant fibrinolysis may occur locally in tissues affected by the disease [
26], with no effects on global fibrinolysis. In spite of ongoing consumption, the levels of plasma fibrinogen are above the normal range in most of these patients. This may stem from parallel persistent fibrinogen production, driven by the substantial inflammation typical to severe COVID-19 [
27]. Due to the coagulopathy in COVID-19 patients, comprehensive studies mapped various coagulation functions in these patients. For example, a recent study provided a comprehensive outlook of the coagulation system in 206 COVID-19 patients, but the levels of FXIII and its possible role in COVID-19 have not yet been examined [
28].
We found low FXIII activity in most of our ICU hospitalized COVID-19 patients, but not in non-severe COVID-19 patients. Extensive serum (not plasma) proteomic analysis of COVID-19 patients pointed to the possibility of decrease in FXIII-B in the sera of COVID-19 patients, in a correlation to increase in IL-6 levels [
29]. In our study, we did not find a correlation between low FXIII activity and inflammation associated parameters (CRP, total neutrophils count). Three possible mechanisms may account for the low levels of FXIII activity in such patients: (1) Inhibition, (2) Reduced production (mostly due to hepatic failure), 3.Consumption. The first mechanism may stem from inhibitory antibodies against FXIII, as autoantibodies are a common finding in COVID-19 patients [
30], and the emergence of autoantibodies is a well-established mechanism in acquired FXIII deficiency [
31]. While the targets of such antibodies in COVID-19 are diverse and include components of the immune system, some may be associated with coagulopathy, such as anti-phospholipid autoantibodies [
30]. However, this mechanism is not supported by our mixing test that complemented the levels of FXIII activity to a normal level, with no evidence of inhibitors in the plasma of the patients. Hepatic dysfunction has been reported in 14-53 % of COVID-19 patients [
32], and since FXIII-B is produced in the liver we examined liver functions in our severe COVID-19 patients. We recorded abnormal liver functions in most of our ICU hospitalized COVID-19 patients, but with no significant difference between patients with low or normal levels of FXIII activity. We found lower albumin levels in patients with low FXIII activity, in agreement with previous studies that demonstrated hypoalbuminemia in severe COVID-19 patients [
33]. It was suggested that the mechanism underlying hypoalbuminemia in COVID-19 patients is albumin excretion into damaged organs [
33]. Since the major cellular storage of FXIII-A in the circulation is within monocytes and platelets [
34], we examined their concentrations in our severe COVID-19 patients, and did not find any significant differences between patients with low or normal FXIII activity levels. Hence, our data indicate that production difficulties may not account for the low FXIII we observed in severe COVID-19 patients, but rather a consumption-based mechanism. This approach is supported by the concomitant reduction in FXIII-A (the catalytic subunit) antigen with the decreased FXIII activity in the severe patients. Consumption accompanies conditions such as inflammation and activation of the coagulation system, both relevant to COVID-19. We show herein that the levels of FXIII activity in the severe COVID-19 patients, are not stable, but rather decline with prolongation of hospitalization, and may be associated with continuous consumption due to the ongoing fibrin deposition in the lungs of these patients.
More data is needed to establish whether low levels of FXIII are involved in mechanisms underlying coagulopathy in severe COVID-19 patients, but previously published experimental data may point to such possibilities; Increased embolism was found in FXIII-/- compared with wild type mice in acute DVT model, apparently due to the effects of FXIII deficiency on clot stability [
35]. Moreover, it was shown that FXIII supplementation stabilizes venous thrombi, and reduces embolism [
36]. In humans, a weak protective effect of increased FXIII activity against VTE was demonstrated [
37]. Moreover, the combination of high D-dimer and low FXIII concentrations was found to be associated with PE, and a threshold of 69 % of FXIII concentration was set to distinguish between confirmed PE and other serious diseases with similar symptoms [
38]. In our cohort, the average level of FXIII activity in the severe patients was similar, 69.8 %, combined with high D-dimer levels in most of our patients. Hence, low FXIII levels may alter thrombi properties, resulting in an increased risk for embolism. The predominant manifestation of FXIII deficiency is bleeding [
39]. We recorded bleeding events in 8/34 (24 %) of our patients which all occurred in patients with low FXIII activity (10/25, 32 % of these patients). Despite considerable coagulopathy in COVID-19, a high prevalence of bleeding has not been reported in this disease [
40]. The overall hypercoagulable state in COVID-19 may overlay bleeding risk factors discussed before [
40], or the low levels of FXIII activity presented in this study.
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