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These studies suggest that ACEI/ARB use is not associated with increased COVID-19 infection risk, severity, or mortality, and may even reduce mortality and hospital stays in certain populations, supporting the continuation of these medications during the pandemic.
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Angiotensin-converting enzyme inhibitors (ACEIs) and angiotensin receptor blockers (ARBs) are commonly prescribed medications for managing hypertension and other cardiovascular conditions. With the onset of the COVID-19 pandemic, concerns emerged regarding the potential impact of these medications on COVID-19 susceptibility, severity, and mortality due to their influence on ACE2, the receptor for SARS-CoV-2.
Several studies have investigated whether ACEI/ARB use increases the risk of contracting COVID-19. A systematic review and meta-analysis involving over 19,000 COVID-19 cases found no significant association between ACEI/ARB exposure and the risk of COVID-19 infection (OR = 0.99; 95% CI, 0.95-1.04). Similarly, another comprehensive review concluded that ACEI/ARB use does not increase ACE2 expression in humans, thereby not elevating the risk of COVID-19 infection.
Multiple studies have consistently shown that ACEI/ARB use does not exacerbate COVID-19 severity or increase mortality. A meta-analysis of 102 studies found no association between prior ACEI/ARB use and severe COVID-19 outcomes or mortality (aOR 0.87, 95% CI 0.66-1.04). Another study confirmed that ACEI/ARB use was not linked to increased severity or mortality in COVID-19 patients (OR 0.73, 95% CI 0.38-1.40).
In East-Asian populations, ACEI/ARB use was associated with a shorter hospital stay and lower mortality (OR = 0.61, 95% CI 0.52-0.70) without affecting disease severity. This suggests potential benefits of ACEI/ARB in reducing mortality among COVID-19 patients in this demographic.
For hypertensive patients hospitalized with COVID-19, ACEI/ARB use was linked to a significantly lower risk of all-cause mortality compared to non-users (adjusted HR 0.42, 95% CI 0.19-0.92). This finding was consistent across various studies, indicating that ACEI/ARB therapy should be continued in hypertensive COVID-19 patients.
The biological mechanisms underlying these observations are complex. While ACEIs and ARBs may theoretically increase ACE2 expression, the actual clinical data do not support an increased risk of COVID-19 infection or worse outcomes. In fact, some studies suggest that ARBs, in particular, may offer protective benefits against severe COVID-19 outcomes .
Current evidence overwhelmingly supports the continued use of ACEIs and ARBs in patients with COVID-19. These medications do not increase the risk of infection, severity, or mortality from COVID-19. On the contrary, they may reduce mortality, especially in hypertensive patients. Therefore, discontinuation of ACEI/ARB therapy in the context of COVID-19 is not recommended. Further research may continue to elucidate the nuanced roles these medications play in the context of COVID-19.
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