Reina-Couto Marta, Alves David, Silva-Pereira Carolina, Pereira-Terra Patrícia, Martins Sandra, Bessa João, Teixeira-Santos Luísa, Pinho Dora, Morato Manuela, Dias Cláudia Camila, Sarmento António, Tavares Margarida, Guimarães João T, Roncon-Albuquerque Roberto, Paiva José-Artur, Albino-Teixeira António, Sousa Teresa
Departamento de Biomedicina - Unidade de Farmacologia e Terapêutica, Faculdade de Medicina da Universidade do Porto (FMUP), Rua Dr. Plácido da Costa, S/N, Edifício Poente, Piso 3, 4200-450, Porto, Portugal.
Centro de Investigação Farmacológica e Inovação Medicamentosa da Universidade do Porto (MEDInUP), Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
Inflamm Res. 2025 Jan 25;74(1):26. doi: 10.1007/s00011-024-01964-8.
Endocan has been scarcely explored in COVID-19, especially regarding its modulation by veno-venous extracorporeal membrane oxygenation (VV-ECMO), hypertension or previous renin-angiotensin-aldosterone system (RAAS) inhibitors treatment. We compared endocan and other endotheliitis markers in hospitalized COVID-19 patients and assessed their modulation by VV-ECMO, hypertension and previous RAAS inhibitors treatment.
Serum endocan, intercellular adhesion molecule-1 (ICAM-1), vascular cell adhesion molecule-1 (VCAM-1) and E-selectin were measured in "severe" (n = 27), "critically ill" (n = 17) and "critically ill on VV-ECMO" (n = 17) COVID-19 patients at admission, days 3-4, 5-8 and weekly thereafter, and in controls (n = 23) at a single time point.
Admission endocan and VCAM-1 were increased in all patients, but "critically ill on VV-ECMO" patients had higher endocan and E-Selectin. Endocan remained elevated throughout hospitalization in all groups. "Severe" and "critically ill" hypertensive patients or previously treated with RAAS inhibitors had higher endocan and/or VCAM-1, but in VV-ECMO patients the raised endocan values seemed unrelated with these factors. Among all COVID-19 hypertensive patients, those with previous RAAS inhibitors treatment had higher endocan.
In our study, endocan stands out as the best marker of endotheliitis in hospitalized COVID-19 patients, being upregulated by VV-ECMO support, hypertension and previous RAAS inhibitor treatment.
内皮糖蛋白(Endocan)在新型冠状病毒肺炎(COVID-19)中的研究较少,尤其是关于其受静脉-静脉体外膜肺氧合(VV-ECMO)、高血压或既往肾素-血管紧张素-醛固酮系统(RAAS)抑制剂治疗的影响。我们比较了住院COVID-19患者体内的内皮糖蛋白和其他内皮炎症标志物,并评估了VV-ECMO、高血压和既往RAAS抑制剂治疗对它们的影响。
在入院时、第3 - 4天、第5 - 8天以及此后每周,对“重症”(n = 27)、“危重症”(n = 17)和“接受VV-ECMO治疗的危重症”(n = 17)COVID-19患者测定血清内皮糖蛋白、细胞间黏附分子-1(ICAM-1)、血管细胞黏附分子-1(VCAM-1)和E-选择素,并在单一时间点对对照组(n = 23)进行测定。
所有患者入院时内皮糖蛋白和VCAM-1均升高,但“接受VV-ECMO治疗的危重症”患者的内皮糖蛋白和E-选择素更高。在所有组中,内皮糖蛋白在整个住院期间均保持升高。“重症”和“危重症”高血压患者或既往接受RAAS抑制剂治疗的患者内皮糖蛋白和/或VCAM-1更高,但在接受VV-ECMO治疗的患者中,内皮糖蛋白升高的值似乎与这些因素无关。在所有COVID-19高血压患者中,既往接受RAAS抑制剂治疗的患者内皮糖蛋白更高。
在我们的研究中,内皮糖蛋白是住院COVID-19患者内皮炎症的最佳标志物,受VV-ECMO支持、高血压和既往RAAS抑制剂治疗上调。