Zhang Yue, Ba Djibril M, Risher Kathryn, Liao Duanping, Parent Leslie J, Ghahramani Nasrollah, Chinchilli Vernon M
Department of Public Health Sciences, Penn State College of Medicine, Hershey, PA, USA.
Department of Medicine, Penn State College of Medicine, Hershey, PA, USA.
Clin Kidney J. 2024 Jun 8;17(7):sfae164. doi: 10.1093/ckj/sfae164. eCollection 2024 Jul.
The association between angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin II receptor blockers (ARBs) and severe acute respiratory syndrome coronavirus 2 susceptibility, particularly via ACE-2 receptor upregulation in the kidneys, raises concerns about potential kidney disease risks in long coronavirus disease (COVID) patients. This study explores the association of ACEI/ARB therapy on acute kidney injury (AKI), chronic kidney disease (CKD) and all-cause mortality in patients with and without long COVID.
A retrospective cohort study using TriNetX datasets was conducted, with diagnoses of long COVID via (ICD-10) codes and prescription for ACEI/ARB as the classification of four cohorts: long COVID ACEI/ARB users (LCAUs), long COVID ACEI/ARB non-users (LCANs), non-long COVID ACEI/ARB users (NLCAUs) and non-long COVID ACEI/ARB non-users (NLCANs). Multivariable stratified Cox proportional hazards regression models assessed the adjusted hazard ratios (aHRs) across groups. Additional analyses were conducted, including time-dependent exposure analysis and comparison with an active comparator, calcium channel blockers.
Our study included 18 168 long COVID and 181 680 propensity score-matched non-long COVID patients from October 2021 to October 2023. ACEI/ARB use did not significantly affect the risk of AKI or CKD when comparing LCAUs with LCANs and NLCAUs with NLCANs. However, a protective effect against all-cause mortality was observed {aHR 0.79 [95% confidence interval (CI) 0.65-0.93]} in the NLCAU group compared with the NLCAN group. Conversely, long COVID was associated with increased risks of CKD [aHR 1.49 (95% CI 1.03-2.14)] and all-cause mortality [aHR 1.49 (95% CI 1.00-2.23)] when comparing LCANs with NLCANs. The additional analyses support the primary findings.
ACEI/ARB treatment does not increase the incidence of CKD or AKI, regardless of long COVID status. However, long COVID itself is associated with increasing risks of kidney diseases and all-cause mortality.
血管紧张素转换酶抑制剂(ACEIs)或血管紧张素II受体阻滞剂(ARBs)与严重急性呼吸综合征冠状病毒2易感性之间的关联,尤其是通过肾脏中ACE-2受体上调,引发了对长期感染冠状病毒病(COVID)患者潜在肾脏疾病风险的担忧。本研究探讨了ACEI/ARB治疗对有或无长期COVID患者的急性肾损伤(AKI)、慢性肾脏病(CKD)和全因死亡率的影响。
利用TriNetX数据集进行了一项回顾性队列研究,通过国际疾病分类第十版(ICD-10)编码诊断长期COVID,并将ACEI/ARB处方作为四个队列的分类依据:长期COVID的ACEI/ARB使用者(LCAUs)、长期COVID的ACEI/ARB非使用者(LCANs)、非长期COVID的ACEI/ARB使用者(NLCAUs)和非长期COVID的ACEI/ARB非使用者(NLCANs)。多变量分层Cox比例风险回归模型评估了各组间的调整后风险比(aHRs)。还进行了额外的分析,包括时间依赖性暴露分析以及与活性对照药物钙通道阻滞剂的比较。
我们的研究纳入了2021年10月至2023年10月期间18168例长期COVID患者和181680例倾向评分匹配的非长期COVID患者。在比较LCAUs与LCANs以及NLCAUs与NLCANs时,使用ACEI/ARB对AKI或CKD的风险没有显著影响。然而,与NLCAN组相比,NLCAU组观察到对全因死亡率有保护作用{aHR 0.79 [95%置信区间(CI)0.65 - 0.93]}。相反,在比较LCANs与NLCANs时,长期COVID与CKD风险增加[aHR 1.49(95% CI 1.03 - 2.14)]和全因死亡率增加[aHR 1.49(95% CI 1.00 - 2.23)]相关。额外的分析支持了主要研究结果。
无论长期COVID状态如何,ACEI/ARB治疗均不会增加CKD或AKI的发生率。然而,长期COVID本身与肾脏疾病风险增加和全因死亡率增加相关。