Department of Anaesthesiology and Intensive Therapy, Hospital of the Ministry of the Interior and Administration, Wrocław, Poland.
Faculty of Medicine, Medical University of Łódź, Łódź, Poland.
Sci Rep. 2024 Apr 3;14(1):7829. doi: 10.1038/s41598-024-58426-8.
The immunotropic effects of aldosterone might play a role in COVID-19, as SARS-CoV-2 reportedly uses angiotensin-converting enzyme 2 receptors as an entry point into cells. Aldosterone function is closely linked to its action on mineralocorticoid receptors in kidneys; it increases the renal retention of sodium and the excretion of potassium, which increases blood pressure. Despite the large number of studies examining the effect of Ang-II and its blockers on the course of COVID-19 infection, there is still uncertainty about the role of aldosterone. The aim of the study was to assess the correlation of aldosterone, urea, creatinine, C-reactive protein (CRP), and procalcitonin (PCT) levels with 28 days of mortality in patients treated for COVID19 in an intensive care unit (ICU). This cross-selection study involved 115 adult patients who were divided into two groups: those who died within a 28-day period (n = 82) and those who survived (n = 33). The correlation of aldosterone, urea, creatinine, C-reactive protein (CRP), and procalcitonin (PCT) levels with 28 days of mortality in patients treated for COVID-19 were performed. The patients' age, sex, scores from the APACHE II, SAPS II, and SOFA scales and comorbidities like HA, IHD and DM were also analyzed. Remarkably, the individuals who survived for 28 days were of significantly lower mean age and achieved notably lower scores on the APACHE II, SAPS II, and SOFA assessment scales. Statistically significantly higher CRP levels were observed on days 3, 5, and 7 in individuals who survived for 28 days. Creatinine levels in the same group were also statistically significantly lower on days 1, 3, and 5 than those of individuals who died within 28 days. The investigation employed both univariate and multivariate Cox proportional hazard regression models to explore factors related to mortality. In the univariate analysis, variables with a p value of less than 0.50 were included in the multivariate model. Age, APACHE II, SAPS II, and SOFA demonstrated significance in univariate analysis and were considered to be associated with mortality. The outcomes of the multivariate analysis indicated that age (HR = 1.03, p = 0.033) served as a robust predictor of mortality in the entire study population. In conclusion the plasma aldosterone level is not associated with ICU mortality in patients with COVID-19. Other factors, including the patient's age, creatinine or CRP contribute to the severity and prognosis of the disease. This study was retrospectively registered in the Australian New Zealand Clinical Trials Registry (ANZCTR) with registration no. ACTRN12621001300864 (27/09/2021: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=382563&isReview=true ).
醛固酮的免疫调节作用可能在 COVID-19 中发挥作用,因为据报道 SARS-CoV-2 使用血管紧张素转换酶 2 受体作为进入细胞的切入点。醛固酮的功能与其在肾脏中的盐皮质激素受体上的作用密切相关;它增加肾脏对钠的保留和钾的排泄,从而升高血压。尽管有大量研究检查了 Ang-II 及其阻滞剂对 COVID-19 感染过程的影响,但醛固酮的作用仍存在不确定性。本研究旨在评估醛固酮、尿素、肌酐、C 反应蛋白(CRP)和降钙素原(PCT)水平与在重症监护病房(ICU)接受 COVID-19 治疗的患者 28 天死亡率之间的相关性。这项横断面研究纳入了 115 名成年患者,他们分为两组:28 天内死亡(n=82)和存活(n=33)。对接受 COVID-19 治疗的患者的醛固酮、尿素、肌酐、C 反应蛋白(CRP)和降钙素原(PCT)水平与 28 天死亡率进行了相关性分析。还分析了患者的年龄、性别、APACHE II、SAPS II 和 SOFA 评分以及合并症,如 HA、IHD 和 DM。值得注意的是,存活 28 天的患者年龄明显较低,APACHE II、SAPS II 和 SOFA 评估量表的评分明显较低。存活 28 天的患者在第 3、5 和 7 天的 CRP 水平显著升高。同一组的肌酐水平在第 1、3 和 5 天也显著低于 28 天内死亡的患者。该研究采用单变量和多变量 Cox 比例风险回归模型来探讨与死亡率相关的因素。在单变量分析中,将 p 值小于 0.50 的变量纳入多变量模型。年龄、APACHE II、SAPS II 和 SOFA 在单变量分析中具有统计学意义,被认为与死亡率相关。多变量分析的结果表明,年龄(HR=1.03,p=0.033)是整个研究人群死亡率的有力预测因素。总之,血浆醛固酮水平与 COVID-19 患者 ICU 死亡率无关。其他因素,包括患者的年龄、肌酐或 CRP,会导致疾病的严重程度和预后。这项研究是在澳大利亚和新西兰临床试验注册中心(ANZCTR)进行的回顾性注册,注册号为 ACTRN12621001300864(2021 年 9 月 27 日:https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=382563&isReview=true)。