Objectives: To evaluate the impact of angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) on coronavirus disease 2019 (COVID-19) patients.
Methods: We included 229 patients with confirmed COVID-19 in a multicenter, retrospective cohort study. Propensity score matching at a ratio of 1:4 was introduced to eliminate the potential confounders. Patients were assigned to the ACEI/ARB group (n=40) or control group (n=160) according to whether they were current users of medication.
Results: Compared to the control group, patients in the ACEI/ARB group had lower levels of plasma IL-1β [(6.27±0.50) vs. (8.23±0.39) pg/ml, P=0.028], IL-8 [(35.74±4.00) vs. (45.88±2.06) pg/ml, P=0.037] and TNF-α [(8.79±0.40) vs. (10.91±0.21) pg/ml, P<0.01]. Patients with the current use of ACEIs/ARBs had a higher risk of shock (23% vs. 8%, P<0.01). Decreased lymphocyte counts [(0.85±0.45) vs. (1.02±0.52)*10^9/L, P=0.041] and elevated plasma levels of IL-10 [(7.39±0.51) vs. (6.18±0.16) pg/ml, P<0.01] were also important discoveries in the ACEI/ARB group. Patients in the ACEI/ARB group had a prolonged duration of viral shedding [(25±7) vs. (20±6) days, P=0.031] and increased length of hospitalization [(23±12) vs. (16±8) days, P<0.01]. These trends were similar in patients with hypertension.
Conclusions: For patients with excessive inflammatory responses and stable hemodynamics, ACEIs or ARBs might be tried to relieve the inflammatory storm, but the antiviral treatment should be enforced and the hemodynamics should be monitored closely; for patients with low levels of proinflammatory factors or instability hemodynamics, the agents might not be used to avoid a delay in viral clearance or increase the risk of shock.

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Posted 08 May, 2020
Posted 08 May, 2020
Objectives: To evaluate the impact of angiotensin-converting enzyme inhibitors (ACEIs) or angiotensin receptor blockers (ARBs) on coronavirus disease 2019 (COVID-19) patients.
Methods: We included 229 patients with confirmed COVID-19 in a multicenter, retrospective cohort study. Propensity score matching at a ratio of 1:4 was introduced to eliminate the potential confounders. Patients were assigned to the ACEI/ARB group (n=40) or control group (n=160) according to whether they were current users of medication.
Results: Compared to the control group, patients in the ACEI/ARB group had lower levels of plasma IL-1β [(6.27±0.50) vs. (8.23±0.39) pg/ml, P=0.028], IL-8 [(35.74±4.00) vs. (45.88±2.06) pg/ml, P=0.037] and TNF-α [(8.79±0.40) vs. (10.91±0.21) pg/ml, P<0.01]. Patients with the current use of ACEIs/ARBs had a higher risk of shock (23% vs. 8%, P<0.01). Decreased lymphocyte counts [(0.85±0.45) vs. (1.02±0.52)*10^9/L, P=0.041] and elevated plasma levels of IL-10 [(7.39±0.51) vs. (6.18±0.16) pg/ml, P<0.01] were also important discoveries in the ACEI/ARB group. Patients in the ACEI/ARB group had a prolonged duration of viral shedding [(25±7) vs. (20±6) days, P=0.031] and increased length of hospitalization [(23±12) vs. (16±8) days, P<0.01]. These trends were similar in patients with hypertension.
Conclusions: For patients with excessive inflammatory responses and stable hemodynamics, ACEIs or ARBs might be tried to relieve the inflammatory storm, but the antiviral treatment should be enforced and the hemodynamics should be monitored closely; for patients with low levels of proinflammatory factors or instability hemodynamics, the agents might not be used to avoid a delay in viral clearance or increase the risk of shock.

Figure 1

Figure 2
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