PREDICTORS OF THROMBOGENICITY AND DEVELOPMENT OF ENDOTHELIITIS IN PATIENTS WITH СOVID-19 — ASSOCIATED CARDIAC AND VASCULAR SURGICAL PATHOLOGY IN THE ACUTE AND POST-COVID PERIODS

O. Klimova, Y. Kalashnikova, O. Lavinska, L. Drozdova, O. Buchneva, O. Tkachuk
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For patients with COVID-19, a characteristic excessive long-term activation of the complement system was revealed, which is manifested by an increase in the level of C3 and C4 components (in the acute period of Covid-19, the level of the C3 component of complement was increased by 83 % and 157 %, respectively, for patients with vascular and cardiac pathology, and the level of the C4 component in these groups exceeded the reference level by 96 % and 124 %, respectively). It was shown that the content of C-reactive protein significantly exceeded the reference level in the acute period of Covid-19 in vascular pathology by 22.7 times, in cardiac pathology by 10.6 times, in the post-covid period this ratio was maintained, namely, in vascular pathology in 26.6 times, with cardiac pathology 15.5 times, that is, in vascular pathology, C-reactive protein was always increased significantly more than in cardiac. Thrombocytopenia, detected in all groups, especially in the acute period of SARS-Cov-2 infection, (vascular pathology — a decrease in the number of platelets by 2 times or by 50 %, cardiac pathology — by 15 %), (vascular pathology in the post-covid period — a decrease by 38 %, cardiac pathology — a decrease of 22.7 %), due to the activation of platelets due to increased thrombin formation and subsequent clearance by the reticulo-endothelial system, activation of thrombus formation and consumption coagulopathy, direct viral-platelet interaction, interaction with immune complexes (antigen + antibody + complement), clearance of platelets due to pronounced endotheliitis in main and capillary vessels. Excessive activation of the complement system along with a significant increase in the content of CRP has a prognostic value for the duration and severity of immunoinflammatory reactions and clinically expressed complications in the distant post-covid period against the background of surgical pathology. A significantly increased concentration of IL-6 in vascular pathology was revealed in the acute period of viral infection by 27.7 times, in the post-viral period by 24.4 times. In cardiac pathology, the concentration of IL-6 was significantly increased in the acute period by 2.5 times, and in the post-epidemic period by 3.2 times due to pro-compensatory and adaptive reactions against the background of suppression of the adhesive and absorbing properties of phagocytic neutrophils. A significant increase in the concentration of IL-18 in the blood serum of all examined patients in the acute period was found: in vascular pathology by 24.6 %, in heart pathology by 70 %, indicating long-term activation of macrophages. Different degrees of increase in complement components and cytokines in the acute period of Covid-19 infection and in the post-covid period may indicate the predominance of one or another inflammatory mechanism in vascular and cardiac pathology. In 100 % of patients with vascular pathology in the acute period, a 79-fold increase in procalcitonin was observed, in the post-covid period — in 50 %, a significant increase of 42 times, with cardiac pathology in the acute period — in 50 % - 43 times, in the post-covid period — in 58 % by 46 times, which indicated the formation of a spectrum of cytotoxic molecules when a bacterial infection occurred and required antibiotic therapy. A significant increase in the concentration of fibrinogen, fibrin, and soluble fibrin-monomeric complexes (FSMC) was observed in all examined groups of patients in all periods. It was proved that the activity of thrombus formation was 4.6 times more pronounced in vascular pathology in the acute period, while in cardiac pathology it was 2 times more pronounced, and in the postoperative period in vascular pathology it was 2.3 times, in cardiac pathology it was 1,8 times. For the first time, it was found that in all examined groups of patients, the concentration of the native physiological anticoagulant antithrombin III was reduced, and this was most pronounced in the group of cardiac pathology in the post-covid period than in vascular, therefore, in cardiac pathology, the anticoagulant properties were the most lost, perhaps even due to not only dependent on viral infection, but also genomic predictors. The change in another link of the hemostasis system indicated the activation of fibrinolysis at the first stage, namely, a significant increase in the concentration of D-dimers in all types of pathology as in acute (vascular pathology — 4.2-fold increase, cardiac pathology — 2.7-fold), and in the post-epidemic periods (vascular pathology — 7.7 times, cardiac pathology — 2.4 times), while it is most pronounced in the group of cardiac pathology in the acute viral period. \nAgainst the background of a significant increase in the content of IL-6 both in the acute and in the remote period after infection with SARS-Cov-2, in 100 % of patients with cardiac pathology, fibrinolytic activity was significantly reduced in connection with the inhibited activity of plasminogen due to the inhibition of the activity of this pro-inflammatory interleukin activator plasminogen. A decrease in the concentration of plasminogen in all examined groups of patients by 18-29.5 % indicated the phenomenon of consumption of plasminogen for the formation of plasmin during the preliminary activation of fibrinolysis against the background of an actual increase in the concentration of fibrin. Possible clinical consequences of a decrease in the concentration of the native physiological anticoagulant antithrombin III and plasminogen in the acute period of SARS-Cov-2 infection and the post-covid period are a decrease in anticoagulant activity, a threat of thrombus formation, a decrease in fibrinolytic activity, and in combination with an increase in the concentration of fibrin, fibrinogen, soluble fibrin monomers complexes and D-dimers — the threat of DIC-syndrome formation. Hemostasiological markers of DIC in the hypercoagulable phase were detected in 6 patients, namely, in the acute period of SARS-Cov-2 infection in 2 patients with cardiac pathology and 1 patient with vascular pathology, in the post-COVID period in 2 patients with cardiac pathology and in 1 patient with abdominal pathology. DIC in the hypocoagulation phase was not detected in any patient. Therefore, the immune-inflammatory reaction to the SARS-CoV-2 viral infection leads to a noticeable activation of coagulation — the process of thrombosis — with signs of systemic endothelial inflammatory damage, namely — endotheliitis, and the subsequent loss of the physiological properties of the endothelium. The general thing, as a rule, is the presence of common patterns, which are manifested in the fact that the SARS-Cov-2 virus interacts with complement proteins and endothelial cells and platelets, which causes an inflammatory reaction in all organs and systems. \nConclusions. \n1. Immunopathological mechanisms formed against the background of the interaction of SARS-Cov-2 proteins with endothelial cells and proteins of the complement system, which form membrane-attacking complexes, lead to violations of the structural and functional organization of endothelial cells in both main and capillary vessels, which leads to pathologies of various organs and pathologies of the hemostasis system. \n2. Thus, the processes occurring in the endothelium are characterized by inflammatory changes that cause activation of the plasma link of hemostasis, which includes coagulation, anticoagulation, and fibrinolysis factors, activation of the complement protein system, changes in the function of platelets and their interaction with endothelial cells, which in various combinations indicate risk of thrombogenicity or DIC. \n3. The revealed regularities of the interaction of factors of innate immunity and the SARS-Cov-2 virus, which contribute to the development of a long-term immunoinflammatory reaction in the form of endotheliitis, require personalized treatment for comorbid conditions, taking into account changes in indicators of immunoresistance and the hemostasis system.","PeriodicalId":405037,"journal":{"name":"Kharkiv Surgical School","volume":"17 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kharkiv Surgical School","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37699/2308-7005.3.2022.04","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Summary. Purpose: to identify early immunoinflammatory predictors of the development of disorders of the hemostasis system (coagulation, anticoagulation, and fibrinolysis) in patients with urgent cardiac and vascular surgical pathology in the conditions of joining the SARS-Cov-2 viral infection and in the long term after infection. The results. For patients with COVID-19, a characteristic excessive long-term activation of the complement system was revealed, which is manifested by an increase in the level of C3 and C4 components (in the acute period of Covid-19, the level of the C3 component of complement was increased by 83 % and 157 %, respectively, for patients with vascular and cardiac pathology, and the level of the C4 component in these groups exceeded the reference level by 96 % and 124 %, respectively). It was shown that the content of C-reactive protein significantly exceeded the reference level in the acute period of Covid-19 in vascular pathology by 22.7 times, in cardiac pathology by 10.6 times, in the post-covid period this ratio was maintained, namely, in vascular pathology in 26.6 times, with cardiac pathology 15.5 times, that is, in vascular pathology, C-reactive protein was always increased significantly more than in cardiac. Thrombocytopenia, detected in all groups, especially in the acute period of SARS-Cov-2 infection, (vascular pathology — a decrease in the number of platelets by 2 times or by 50 %, cardiac pathology — by 15 %), (vascular pathology in the post-covid period — a decrease by 38 %, cardiac pathology — a decrease of 22.7 %), due to the activation of platelets due to increased thrombin formation and subsequent clearance by the reticulo-endothelial system, activation of thrombus formation and consumption coagulopathy, direct viral-platelet interaction, interaction with immune complexes (antigen + antibody + complement), clearance of platelets due to pronounced endotheliitis in main and capillary vessels. Excessive activation of the complement system along with a significant increase in the content of CRP has a prognostic value for the duration and severity of immunoinflammatory reactions and clinically expressed complications in the distant post-covid period against the background of surgical pathology. A significantly increased concentration of IL-6 in vascular pathology was revealed in the acute period of viral infection by 27.7 times, in the post-viral period by 24.4 times. In cardiac pathology, the concentration of IL-6 was significantly increased in the acute period by 2.5 times, and in the post-epidemic period by 3.2 times due to pro-compensatory and adaptive reactions against the background of suppression of the adhesive and absorbing properties of phagocytic neutrophils. A significant increase in the concentration of IL-18 in the blood serum of all examined patients in the acute period was found: in vascular pathology by 24.6 %, in heart pathology by 70 %, indicating long-term activation of macrophages. Different degrees of increase in complement components and cytokines in the acute period of Covid-19 infection and in the post-covid period may indicate the predominance of one or another inflammatory mechanism in vascular and cardiac pathology. In 100 % of patients with vascular pathology in the acute period, a 79-fold increase in procalcitonin was observed, in the post-covid period — in 50 %, a significant increase of 42 times, with cardiac pathology in the acute period — in 50 % - 43 times, in the post-covid period — in 58 % by 46 times, which indicated the formation of a spectrum of cytotoxic molecules when a bacterial infection occurred and required antibiotic therapy. A significant increase in the concentration of fibrinogen, fibrin, and soluble fibrin-monomeric complexes (FSMC) was observed in all examined groups of patients in all periods. It was proved that the activity of thrombus formation was 4.6 times more pronounced in vascular pathology in the acute period, while in cardiac pathology it was 2 times more pronounced, and in the postoperative period in vascular pathology it was 2.3 times, in cardiac pathology it was 1,8 times. For the first time, it was found that in all examined groups of patients, the concentration of the native physiological anticoagulant antithrombin III was reduced, and this was most pronounced in the group of cardiac pathology in the post-covid period than in vascular, therefore, in cardiac pathology, the anticoagulant properties were the most lost, perhaps even due to not only dependent on viral infection, but also genomic predictors. The change in another link of the hemostasis system indicated the activation of fibrinolysis at the first stage, namely, a significant increase in the concentration of D-dimers in all types of pathology as in acute (vascular pathology — 4.2-fold increase, cardiac pathology — 2.7-fold), and in the post-epidemic periods (vascular pathology — 7.7 times, cardiac pathology — 2.4 times), while it is most pronounced in the group of cardiac pathology in the acute viral period. Against the background of a significant increase in the content of IL-6 both in the acute and in the remote period after infection with SARS-Cov-2, in 100 % of patients with cardiac pathology, fibrinolytic activity was significantly reduced in connection with the inhibited activity of plasminogen due to the inhibition of the activity of this pro-inflammatory interleukin activator plasminogen. A decrease in the concentration of plasminogen in all examined groups of patients by 18-29.5 % indicated the phenomenon of consumption of plasminogen for the formation of plasmin during the preliminary activation of fibrinolysis against the background of an actual increase in the concentration of fibrin. Possible clinical consequences of a decrease in the concentration of the native physiological anticoagulant antithrombin III and plasminogen in the acute period of SARS-Cov-2 infection and the post-covid period are a decrease in anticoagulant activity, a threat of thrombus formation, a decrease in fibrinolytic activity, and in combination with an increase in the concentration of fibrin, fibrinogen, soluble fibrin monomers complexes and D-dimers — the threat of DIC-syndrome formation. Hemostasiological markers of DIC in the hypercoagulable phase were detected in 6 patients, namely, in the acute period of SARS-Cov-2 infection in 2 patients with cardiac pathology and 1 patient with vascular pathology, in the post-COVID period in 2 patients with cardiac pathology and in 1 patient with abdominal pathology. DIC in the hypocoagulation phase was not detected in any patient. Therefore, the immune-inflammatory reaction to the SARS-CoV-2 viral infection leads to a noticeable activation of coagulation — the process of thrombosis — with signs of systemic endothelial inflammatory damage, namely — endotheliitis, and the subsequent loss of the physiological properties of the endothelium. The general thing, as a rule, is the presence of common patterns, which are manifested in the fact that the SARS-Cov-2 virus interacts with complement proteins and endothelial cells and platelets, which causes an inflammatory reaction in all organs and systems. Conclusions. 1. Immunopathological mechanisms formed against the background of the interaction of SARS-Cov-2 proteins with endothelial cells and proteins of the complement system, which form membrane-attacking complexes, lead to violations of the structural and functional organization of endothelial cells in both main and capillary vessels, which leads to pathologies of various organs and pathologies of the hemostasis system. 2. Thus, the processes occurring in the endothelium are characterized by inflammatory changes that cause activation of the plasma link of hemostasis, which includes coagulation, anticoagulation, and fibrinolysis factors, activation of the complement protein system, changes in the function of platelets and their interaction with endothelial cells, which in various combinations indicate risk of thrombogenicity or DIC. 3. The revealed regularities of the interaction of factors of innate immunity and the SARS-Cov-2 virus, which contribute to the development of a long-term immunoinflammatory reaction in the form of endotheliitis, require personalized treatment for comorbid conditions, taking into account changes in indicators of immunoresistance and the hemostasis system.
急性期和后冠期Сovid-19相关心脏和血管外科病理患者血栓形成性和内皮炎发展的预测因素
总结。目的:在加入SARS-Cov-2病毒感染的情况下和感染后的长期内,确定急诊心脏和血管外科病理患者止血系统(凝血、抗凝和纤溶)功能障碍发展的早期免疫炎症预测因子。结果。COVID-19患者,长期过度激活补体系统的特点是透露,这是通过增加水平的C3和C4组件(COVID-19的急性期,补语的C3组件增加了83%和157%,分别为患者血管和心脏病理,和这些群体的C4组件水平超过了参考水平96%和124%,分别)。结果表明,c反应蛋白含量在Covid-19急性期血管病理中显著高于参考水平22.7倍,心脏病理中显著高于参考水平10.6倍,在Covid-19后时期这一比例保持不变,即血管病理为26.6倍,心脏病理为15.5倍,即血管病理中c反应蛋白含量始终明显高于心脏。在所有组中,特别是在SARS-Cov-2感染的急性期检测到血小板减少(血管病理-血小板数量减少2倍或50%,心脏病理-减少15%),(冠状病毒后血管病理-减少38%,心脏病理-)下降22.7%),这是由于凝血酶形成增加和随后被网状内皮系统清除导致的血小板活化、血栓形成的活化和消耗凝血功能障碍、病毒-血小板直接相互作用、与免疫复合物(抗原+抗体+补体)的相互作用、主要血管和毛细血管内皮炎引起的血小板清除。在手术病理背景下,补体系统的过度激活以及CRP含量的显著增加对covid后长期免疫炎症反应的持续时间和严重程度以及临床表达的并发症具有预后价值。血管病理中IL-6浓度在病毒感染急性期升高27.7倍,病毒感染后升高24.4倍。在心脏病理中,IL-6浓度在急性期显著升高2.5倍,在疫后期显著升高3.2倍,这是由于在吞噬中性粒细胞粘附和吸收特性受到抑制的背景下,发生了促代偿和适应性反应。所有检查的患者急性期血清IL-18浓度均显著升高:血管病理升高24.6%,心脏病理升高70%,表明巨噬细胞长期活化。补体成分和细胞因子在Covid-19感染急性期和Covid-19后时期的不同程度增加,可能表明一种或另一种炎症机制在血管和心脏病理中占主导地位。在100%的急性期血管病理患者中,观察到降钙素原增加了79倍,在covid后时期-增加了50%,显着增加了42倍,心脏病理在急性期-增加了50% - 43倍,在covid后时期-增加了58% - 46倍,这表明当细菌感染发生并需要抗生素治疗时形成了细胞毒性分子谱。纤维蛋白原、纤维蛋白和可溶性纤维蛋白单体复合物(FSMC)的浓度在所有检查组的患者中均显著升高。证明急性期血管病理血栓形成的活动性是急性期血栓形成活动性的4.6倍,心脏病理血栓形成活动性是急性期血栓形成活动性的2倍,术后血管病理血栓形成活动性是急性期血栓形成活动性的2.3倍,心脏病理血栓形成活动性是急性期血栓形成活动性的1.8倍。首次发现,在所有检查的患者组中,天然生理性抗凝血酶III的浓度降低,这在心脏病理组中比在血管病理组中更为明显,因此,在心脏病理组中,抗凝血特性损失最大,甚至可能不仅取决于病毒感染,还取决于基因组预测因子。止血系统另一环节的变化表明第一阶段纤维蛋白溶解的激活,即在所有病理类型中d -二聚体浓度显著增加,如急性期(血管病理- 4.2倍,心脏病理- 2.7倍)和流行后时期(血管病理- 7.7倍,心脏病理- 2倍)。
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