Willems Loes H, Jacobs Lotte M C, Groh Laszlo A, Ten Cate Hugo, Spronk Henri M H, Wilson-Storey Boden, Hannink Gerjon, van Kuijk Sander M J, Ghossein-Doha Chahinda, Nagy Magdi, Thijssen Dick H J, van Petersen André S, Warlé Michiel C
Department of Surgery, Radboud University Medical Centre, 6525 GA Nijmegen, The Netherlands.
Departments of Internal Medicine and Biochemistry, MUMC and CARIM School for Cardiovascular Diseases, 6229 ER Maastricht, The Netherlands.
J Clin Med. 2023 Feb 10;12(4):1413. doi: 10.3390/jcm12041413.
Among its effect on virtually all other organs, COVID-19 affects the cardiovascular system, potentially jeopardizing the cardiovascular health of millions. Previous research has shown no indication of macrovascular dysfunction as reflected by carotid artery reactivity, but has shown sustained microvascular dysfunction, systemic inflammation, and coagulation activation at 3 months after acute COVID-19. The long-term effects of COVID-19 on vascular function remain unknown.
This cohort study involved 167 patients who participated in the COVAS trial. At 3 months and 18 months after acute COVID-19, macrovascular dysfunction was evaluated by measuring the carotid artery diameter in response to cold pressor testing. Additionally, plasma endothelin-1, von Willebrand factor, Interleukin(IL)-1ra, IL-6, IL-18, and coagulation factor complexes were measured using ELISA techniques.
The prevalence of macrovascular dysfunction did not differ between 3 months (14.5%) and 18 months (11.7%) after COVID-19 infection ( = 0.585). However, there was a significant decrease in absolute carotid artery diameter change, 3.5% ± 4.7 vs. 2.7% ± 2.5, -0.001, respectively. Additionally, levels of vWF:Ag were persistently high in 80% of COVID-19 survivors, reflecting endothelial cell damage and possibly attenuated endothelial function. Furthermore, while levels of the inflammatory cytokines interleukin(IL)-1RA and IL-18 were normalized and evidence of contact pathway activation was no longer present, the concentrations of IL-6 and thrombin:antithrombin complexes were further increased at 18 months versus 3 months (2.5 pg/mL ± 2.6 vs. 4.0 pg/mL ± 4.6, = 0.006 and 4.9 μg/L ± 4.4 vs. 18.2 μg/L ± 11.4, < 0.001, respectively).
This study shows that 18 months after COVID-19 infection, the incidence of macrovascular dysfunction as defined by a constrictive response during carotid artery reactivity testing is not increased. Nonetheless, plasma biomarkers indicate sustained endothelial cell activation (vWF), systemic inflammation (IL-6), and extrinsic/common pathway coagulation activation (FVII:AT, TAT) 18 months after COVID-19 infection.
新型冠状病毒肺炎(COVID-19)几乎对所有其他器官都有影响,它还会影响心血管系统,可能危及数百万人的心血管健康。先前的研究未显示出颈动脉反应性所反映的大血管功能障碍迹象,但显示在急性COVID-19感染后3个月存在持续性微血管功能障碍、全身炎症和凝血激活。COVID-19对血管功能的长期影响仍然未知。
这项队列研究纳入了参与COVAS试验的167例患者。在急性COVID-19感染后的3个月和18个月,通过测量冷加压试验时的颈动脉直径来评估大血管功能障碍。此外,使用酶联免疫吸附测定(ELISA)技术检测血浆内皮素-1、血管性血友病因子、白细胞介素(IL)-1受体拮抗剂、IL-6、IL-18和凝血因子复合物。
COVID-19感染后3个月(14.5%)和18个月(11.7%)大血管功能障碍的患病率无差异(P = 0.585)。然而,颈动脉绝对直径变化显著降低,分别为3.5%±4.7和2.7%±2.5,P = -0.001。此外,80%的COVID-19幸存者血管性血友病因子抗原(vWF:Ag)水平持续升高,反映了内皮细胞损伤以及可能减弱的内皮功能。此外,虽然炎症细胞因子IL-1受体拮抗剂和IL-18水平恢复正常且接触途径激活的证据不再存在,但与3个月时相比,18个月时IL-6和凝血酶:抗凝血酶复合物的浓度进一步升高(分别为2.5 pg/mL±2.6和4.0 pg/mL±4.6,P = 0.006;4.9 μg/L±4.4和18.2 μg/L±11.4,P < 0.001)。
本研究表明,在COVID-19感染18个月后,颈动脉反应性测试中由收缩反应定义的大血管功能障碍发生率并未增加。尽管如此,血浆生物标志物表明在COVID-19感染18个月后存在持续的内皮细胞激活(vWF)、全身炎症(IL-6)和外源性/共同途径凝血激活(FVII:AT,TAT)。