Department of Pediatric Cardiology, Saarland University Medical Center, Homburg/Saar, Germany.
Department of Clinical Chemistry and Laboratory Medicine, Saarland University Medical Center, Homburg/Saar, Germany.
Clin Res Cardiol. 2022 Feb;111(2):154-162. doi: 10.1007/s00392-020-01782-y. Epub 2020 Dec 5.
Angiotensin-converting enzyme (ACE) 2 is known to be a functional receptor for SARS-CoV-2 in the current pandemic. Soluble ACE2 (sACE2) concentrations are elevated in patients with various cardiovascular disorders including heart failure.
In a total of 182 consecutive adult patients with complex congenital heart disease (CHD) and 63 healthy controls, sACE2 concentrations were measured in serum using the Human ACE2 assay by Cloud-Clone Corporation and associated with clinical, laboratory and echocardiographic parameters.
Median sACE2 levels were increased in patients with complex CHD as compared to healthy controls (761.9 pg/ml vs 365.2 pg/ml, p < 0.001). Moreover, sACE2 concentrations were significantly elevated in patients with a higher NYHA class ≥ III (1856.2 pg/ml vs 714.5 pg/ml in patients with NYHA class I/II, p < 0.001). Using linear regression analysis, higher sACE2 levels were associated with a higher NYHA class ≥ III, more severe CHD, a morphological left systemic ventricle, higher creatinine and the use of mineralocorticoid receptor antagonists (MRA) in the univariable model. The use of ACE inhibitors or angiotensin receptor blockers (ARB) was associated with lower sACE2 levels. In the multivariable model, higher sACE2 levels were independently associated with a higher NYHA class ≥ III (p = 0.002) and lower sACE2 levels with the use of ACE inhibitors or ARB (p = 0.001).
Soluble ACE2 concentrations were significantly increased in all types of complex CHD with highest levels found in patients with NYHA class ≥ III. Moreover, a higher NYHA class ≥ III was the most significant determinant that was independently associated with elevated sACE2 concentrations.
血管紧张素转换酶 2(ACE2)是当前大流行中 SARS-CoV-2 的功能受体。可溶性 ACE2(sACE2)浓度在包括心力衰竭在内的各种心血管疾病患者中升高。
在总共 182 例患有复杂先天性心脏病(CHD)的连续成年患者和 63 名健康对照者中,使用 Cloud-Clone Corporation 的 Human ACE2 测定法测量血清中的 sACE2 浓度,并将其与临床、实验室和超声心动图参数相关联。
与健康对照者相比,患有复杂 CHD 的患者的中位 sACE2 水平升高(761.9 pg/ml 比 365.2 pg/ml,p<0.001)。此外,NYHA 分级更高(≥III 级)的患者的 sACE2 浓度显著升高(NYHA 分级 I/II 级患者为 1856.2 pg/ml,p<0.001)。使用线性回归分析,较高的 sACE2 水平与更高的 NYHA 分级≥III 级、更严重的 CHD、形态学左心室系统、更高的肌酐水平和使用盐皮质激素受体拮抗剂(MRA)相关。ACE 抑制剂或血管紧张素受体阻滞剂(ARB)的使用与较低的 sACE2 水平相关。在多变量模型中,较高的 sACE2 水平与更高的 NYHA 分级≥III 级独立相关(p=0.002),而 ACE 抑制剂或 ARB 的使用与较低的 sACE2 水平相关(p=0.001)。
在所有类型的复杂 CHD 中,sACE2 浓度均显著升高,NYHA 分级≥III 级的患者中浓度最高。此外,更高的 NYHA 分级≥III 级是与升高的 sACE2 浓度独立相关的最显著决定因素。