key: cord-1051427-4q8uum72 authors: Perna, Alessandra F.; Capolongo, Giovanna; Trepiccione, Francesco; Simeoni, Mariadelina; Zacchia, Miriam; Ingrosso, Diego title: COVID-19, Low-Molecular-Weight Heparin, and Hemodialysis date: 2020-05-25 journal: Kidney Blood Press Res DOI: 10.1159/000508460 sha: e82bda9e78b47fda3ebd29010b1c515239947d52 doc_id: 1051427 cord_uid: 4q8uum72 nan In an Italian experience, among 200 patients 18 were infected and isolated (9%), and in another unit of 170 patients only 4 were infected [5] . In the Piedmont and Aosta regions, among 2,893 patients 98 were infected (3.4%) during the first month of the epidemic [6] . By the way, in none of the mentioned studies was the mode of anticoagulation during hemodialysis mentioned. While they cast doubts on the open-space hospital model now implemented in many hospitals, which is incompatible with the need to counteract epidemics [7] , these reports also create uncertainty regarding the concept that these patients are at a particularly increased risk for COVID-19. Heparin actually consists of a heterogeneous mixture of sulfomucopolysaccharides, containing also a minimum peptide component of 2 amino acids (glycine and serine). Heparin exerts a binding capacity to both the endothelial surface and various plasmaproteins (Fig. 1) . The molecular weight range of unfractionated heparin (UFH) is 5,000-30,000. Low-molecularweight heparin (LMWH) fractions effectively inhibit the activated factor X (Factor X a ), while exerting a less inhibitory effect on thrombin, compared to the unfractionated forms. It has been shown that LMWH preparations retain their efficacy toward thromboembolisms and, compared to UFH, show increased bioavailability and the need for less frequent administration. Heparin biological activity crucially depends on the endogenous antithrombin anticoagulant [8, 9] . The serine protease inhibitor activity of antithrombin is exerted toward thrombin and Factor X a , resulting in the inhibition of both ( Fig. 1 ) [10] . Congenital or acquired antithrombin deficiency is indeed associated with a high risk of thromboembolic complications and an impaired interaction with heparin. Administration of antithrombin is generally indicated for the prophylaxis of thromboembolic accidents in nephrology (e.g., in patients with nephrotic syndrome) [11] . In addition, it has been shown that during sepsis activation of the extrinsic coagulation pathway, together with a relevant decline of both coagulation inhibition and fibrinolytic mechanisms, may result in a procoagulant state, leading to microvascular thrombosis and multiorgan dysfunction [12] . Antithrombin levels decrease in sepsis and, when low, may predict high mortality [13] . In addition, heparin is utilized in this context, also for its immunomodulatory and anti-inflammatory role [14] . During hemodialysis it is necessary to perform anticoagulation of the dialysis circuit to avoid blood clotting in the system due to Factor VII, platelet, and leukocyte activation. Anticoagulation is usually performed utilizing heparin, often in Western Europe in the lowmolecular-weight form [15, 16] , which has some advantages over UFH. Relative to UFH, in fact, LMWH could induce less undesired bleeding after completion of the dialysis session and perhaps less triglyceride reduction. Heparin-induced thrombocytopenia (HIT) is an immune complex-mediated condition defined as a decrease in platelet counts below 150,000 per mm 3 , with a median nadir of about 55,000 per mm 3 , associated with a positive test for heparin-dependent antibodies [17, 18] . The typical onset pattern (60% of the cases) results in a platelet decline 5-10 days after exposure. The rapid onset pattern (30% of cases) occurs right after the exposure. The delayed onset pattern (∼10%) occurs 9.2 days after the start of heparin administration therapy, on average, although signs and symptoms may occur up to 3 weeks after the exposure [18] . Careful evaluation and monitoring should be indeed applied toward the risk of HIT [19] . LMWH offers the advantage of a reduced binding to platelet factor 4, thus decreasing the HIT risk [20] . On the other hand, the shorter size of LMWH may hamper the effectiveness of protamine as an antidote [20] . Useful information is provided by reporting a thrombocyte count of less than 50%, which represents an important red flag [19, 20] . Laboratory tests can then be used to confirm the presence of platelet factor 4 (PF4)/heparin antibodies [21] . Attention should be payed when reporting the presence of activating antibodies against PF4-heparin complexes (PF4-H) to the cut-off point for a positive test (e.g., 1 U/mL) [19] . A score has been developed based on 8 clinical features, each scoring between -2 and +3 [22] . Other scoring systems are also available [18] . Mechanism of action of UFH and LMWH with the major ligand-binding interactions involved. One of the key proteins for the activity of heparin is antithrombin, a serine protease inhibitor (SERPINSC1) that inactivates several clotting factors. Mechanistically, heparin binds to antithrombin, thus exposing the antithrombin protease inhibitor binding site and forming equimolecular complexes with its ligands. Antithrombin uses unique and extensive conformational change mechanisms to inhibit its protease ligands [8] . Heparin increases by orders of magnitude the tendency of antithrombin to interact with a number of plasma proteins. The resulting complex, in particular with thrombin (factor IIa) and factors IXa, Xia, and Xa, inhibits the protease activities of these clotting factors. Heparin indeed works as an antithrombin-protease-inhibiting cofactor without being consumed, and, once the antithrombin-protease complex is formed, heparin is released in its intact conformation, thus repeatedly activating new antithrombin molecules. Heparin biological activity crucially depends indeed on the endogenous antithrombin anticoagulant activity. The role of antithrombin is pivotal in coagulation regulation by shifting thrombin from procoagulant to anticoagulant activity. The presence of heparin dramatically increases the complex stability of antithrombin with the above-mentioned coagulation factors [8, 9] . One important difference between UFH and LMWH is that the interaction of antithrombin with UHF almost equally induces inhibition and degradation of both Xa and thrombin, while LMWH preferentially determines degradation of factor Xa. Various other potential benefits of heparin in COVID-19 have been put forward recently [28] . LMWH has some antiviral properties in vitro and it is routinely used in COVID-19 patients to prevent or circumvent the activation of the coagulation cascade induced by inflammation [23] . This is a particularly severe and lethal complication, leading to disseminated intravascular coagulation and venous thromboembolism. In a retrospective study, LMWH therapy reduced interleukin-6 release and activity, which is responsible of the "cytokine storm," and treated patients had also a higher percentage of lymphocytes [24] . LMWH therapy is also associated with better outcomes in severe COVID-19 patients with sepsis-induced coagulopathy and markedly elevated D-dimer levels [25] . It should be pointed out that uremia offers a unique microenvironment in which the coagulation and anticoagulation balance can be dysregulated in many ways. For example, the presence of anti-protein C and anti-protein S antibodies has been detected [26] , which may critically underscore the acute onset of a procoagulant situation in these patients (already characterized by an increased thrombotic risk). These data indeed may prudentially pose the indication of monitoring protein C and free protein S (Fig. 2) . It can be hypothesized that, upon SARS-Cov-2 infection, the presence of antibodies with potential inhibitory activity on protein C and protein S may even increase the functional effect of an activated protein C (APC) resistance condition, whereas already present in the patient. Testing for APC resistance is indeed advised in these patients. [29] . Protein S in turn is a cofactor of APC for the inactivation of activated coagulation factors VIII a and V a . Only free protein S, i.e., the fraction which is not bound to C4b-binding protein (not shown) in circulation, retains its anticoagulant activity. Activated factor V (factor V a ) procoagulant activity is inactivated by APC-catalyzed cleavage at the Arg506 level, yielding factor V i . Beyond its intrinsic procoagulant activity, Factor V a also exerts an anticoagulant activity as a cofactor for APC and protein S, in inactivation of the procoagulant factor VIII a yielding factor VIII i [30] . This function is also compromised in the presence of factor V resistance to cleavage by APC (APC-R; hatched box), mainly due to the Arg506Gln mutation (factor V Leiden ), which indeed represents the most common cause of APC resistance in the population. It is therefore possible that hemodialysis patients could be protected with respect to COVID-19 virus infection by the LMWH used in every hemodialysis session. We propose monitoring, in these patients, of the Anti-Factor Xa activity assay [27] , as well as antithrombin, and D-dimer levels, and not just aPTT, in order to possibly even increase the LMWH dosage, in this pandemic period ( Table 1) . The availability of these exams could therefore lead to optimization of LMWH in this patient population. A.F.P. and D.I. received funding from Gnosis, SpA, and EUTox. None. All of the authors contributed equally to the writing of this paper. 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