From the Department of Biomedical Science and Engineering (M.S., S.Y.), Gwangju Institute of Science and Technology, Republic of Korea.
Department of Internal Medicine, Armed Forces Goyang Hospital, Goyang-si, Republic of Korea (J.S.).
Hypertension. 2020 Sep;76(3):742-749. doi: 10.1161/HYPERTENSIONAHA.120.15464. Epub 2020 Jul 13.
The severe acute respiratory syndrome coronavirus 2 is known to infect host cells by interacting with ACE2 (angiotensin-converting enzyme 2) expressed in the respiratory epithelium. There have been concerns on whether alterations of ACE2 expression by renin-angiotensin-aldosterone system (RAAS) inhibitors would contribute to the infectivity and severity of coronavirus disease 2019 (COVID-19). We performed a case-control study to investigate the association between RAAS inhibitors and risk and severity of COVID-19 infection in South Korea using the population-based data provided by the Korean National Health Insurance System. Of 16 281 subjects with hypertension, there were 950 (5.8%) confirmed COVID-19 cases. After case-control matching, multivariable-adjusted conditional logistic regression analysis was performed. The adjusted odds ratio and 95% CIs for COVID-19 infection and long-term hospitalization comparing exposure to RAAS inhibitors and nonexposure to RAAS inhibitors was 1.161 (0.958-1.407) and 0.863 (0.533-1.397), respectively. When comparing exposure to RAAS inhibitors and nonexposure to RAAS inhibitors for intensive care unit admission, high-flow oxygen therapy, and death, the adjusted odds ratios (95% CIs) were 1.515 (0.402-5.701), 0.663 (0.272-1.619), and 1.363 (0.513-3.662), respectively. In all analyses, values were not significant (>0.05). The present study demonstrates the absence of an identifiable association between the exposure to RAAS inhibitors and risk and severity of COVID-19 infection, supporting the current medical guidelines and recommendations that patients should not discontinue RAAS inhibitors out of a concern that they are at increased risk for infection or severe illness of COVID-19.
严重急性呼吸综合征冠状病毒 2 已知通过与呼吸道上皮细胞中表达的 ACE2(血管紧张素转换酶 2)相互作用来感染宿主细胞。人们一直担心肾素-血管紧张素-醛固酮系统 (RAAS) 抑制剂对 ACE2 表达的改变是否会导致 2019 年冠状病毒病 (COVID-19) 的传染性和严重程度增加。我们使用韩国国家健康保险系统提供的基于人群的数据,进行了一项病例对照研究,以调查 RAAS 抑制剂与韩国高血压患者 COVID-19 感染风险和严重程度之间的关系。在 16281 名高血压患者中,有 950 名(5.8%)确诊 COVID-19 病例。在病例对照匹配后,进行了多变量调整的条件逻辑回归分析。与暴露于 RAAS 抑制剂和未暴露于 RAAS 抑制剂相比,COVID-19 感染和长期住院的调整后优势比(95%CI)分别为 1.161(0.958-1.407)和 0.863(0.533-1.397)。当比较 RAAS 抑制剂暴露和未暴露于 RAAS 抑制剂的 ICU 入院、高流量氧疗和死亡时,调整后的优势比(95%CI)分别为 1.515(0.402-5.701)、0.663(0.272-1.619)和 1.363(0.513-3.662)。在所有分析中, 值均无统计学意义(>0.05)。本研究表明,暴露于 RAAS 抑制剂与 COVID-19 感染的风险和严重程度之间没有可识别的关联,支持当前的医学指南和建议,即不应因担心感染或 COVID-19 严重疾病的风险增加而停止使用 RAAS 抑制剂。