Division of Clinical Physiology, Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Department of Cardiology, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.
Geroscience. 2021 Feb;43(1):19-29. doi: 10.1007/s11357-020-00300-2. Epub 2021 Jan 20.
Coronavirus disease 2019 (COVID-19) has a high mortality in elderly patients with pre-existing cardiovascular diseases. The cellular receptor of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the angiotensin-converting enzyme 2 (ACE2), thereby implicating a link between cardiovascular diseases and SARS-CoV-2 susceptibility. Aortic stenosis (AS) represents a chronic inflammatory state with severe cardiovascular complications in the elderly, a prime condition for COVID-19 mortality. The circulating ACE2 levels were measured in 111 patients with severe AS and compared to patients with hypertension and healthy individuals. About 4 times higher circulating ACE2 activity was found in patients with severe AS than in hypertensives or healthy individuals (88.3 ± 61.6., n = 111, 20.6 ± 13.4, n = 540, and 16.1 ± 7.4 mU/L, n = 46, respectively). Patients with severe AS were older than patients with hypertension (80 ± 6 years vs. 60 ± 15 years, P < 0.05). Serum ACE2 activity correlated negatively with the left ventricular ejection fraction, aortic root area, TAPSE, and positively with the right ventricular systolic pressure, cardiac diameters in patients with AS. In contrast, circulating ACE2 activity was independent of the blood pressure, peak flow velocity at the aortic root, kidney function (GFR), and inflammatory state (CRP). We found no effect of RAAS inhibitory drugs on the serum ACE2 activity in this group of patients. Our results illustrate circulating ACE2 as a potential interface between chronic inflammation, cardiovascular disease, and COVID-19 susceptibility. Elderly patients with AS have markedly elevated ACE2 levels together with altered left and right ventricular functions, which may pose higher risks during COVID-19. Our clinical data do not support a role for RAAS inhibitors in regulating circulating ACE2 levels.
2019 年冠状病毒病(COVID-19)在患有先前存在的心血管疾病的老年患者中具有高死亡率。严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的细胞受体是血管紧张素转换酶 2(ACE2),从而暗示心血管疾病与 SARS-CoV-2 易感性之间存在联系。主动脉瓣狭窄(AS)代表一种慢性炎症状态,在老年人中伴有严重心血管并发症,是 COVID-19 死亡率的主要条件。在 111 例严重 AS 患者中测量了循环 ACE2 水平,并与高血压患者和健康个体进行了比较。与高血压患者或健康个体相比,严重 AS 患者的循环 ACE2 活性高约 4 倍(分别为 88.3±61.6、20.6±13.4 和 16.1±7.4 mU/L,n=111、n=540 和 n=46)。严重 AS 患者比高血压患者年龄大(80±6 岁比 60±15 岁,P<0.05)。AS 患者的血清 ACE2 活性与左心室射血分数、主动脉根部面积、TAPSE 呈负相关,与右心室收缩压、心脏直径呈正相关。相比之下,循环 ACE2 活性与血压、主动脉根部峰值流速、肾功能(GFR)和炎症状态(CRP)无关。我们在这组患者中没有发现 RAAS 抑制药物对血清 ACE2 活性的影响。我们的研究结果表明,循环 ACE2 是慢性炎症、心血管疾病和 COVID-19 易感性之间的潜在界面。患有 AS 的老年患者 ACE2 水平显著升高,同时伴有左、右心室功能改变,这可能使他们在 COVID-19 期间面临更高的风险。我们的临床数据不支持 RAAS 抑制剂在调节循环 ACE2 水平中的作用。