BMC Infectious Diseases (Mar 2021)

Renin-angiotensin system inhibitors and susceptibility to COVID-19 in patients with hypertension: a propensity score-matched cohort study in primary care

  • Shamil Haroon,
  • Anuradhaa Subramanian,
  • Jennifer Cooper,
  • Astha Anand,
  • Krishna Gokhale,
  • Nathan Byne,
  • Samir Dhalla,
  • Dionisio Acosta-Mena,
  • Thomas Taverner,
  • Kelvin Okoth,
  • Jingya Wang,
  • Joht Singh Chandan,
  • Christopher Sainsbury,
  • Dawit Tefra Zemedikun,
  • G. Neil Thomas,
  • Dhruv Parekh,
  • Tom Marshall,
  • Elizabeth Sapey,
  • Nicola J. Adderley,
  • Krishnarajah Nirantharakumar

DOI
https://doi.org/10.1186/s12879-021-05951-w
Journal volume & issue
Vol. 21, no. 1
pp. 1 – 14

Abstract

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Abstract Introduction Renin-angiotensin system (RAS) inhibitors have been postulated to influence susceptibility to Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). This study investigated whether there is an association between their prescription and the incidence of COVID-19 and all-cause mortality. Methods We conducted a propensity-score matched cohort study comparing the incidence of COVID-19 among patients with hypertension prescribed angiotensin-converting enzyme I (ACE) inhibitors or angiotensin II type-1 receptor blockers (ARBs) to those treated with calcium channel blockers (CCBs) in a large UK-based primary care database (The Health Improvement Network). We estimated crude incidence rates for confirmed/suspected COVID-19 in each drug exposure group. We used Cox proportional hazards models to produce adjusted hazard ratios for COVID-19. We assessed all-cause mortality as a secondary outcome. Results The incidence rate of COVID-19 among users of ACE inhibitors and CCBs was 9.3 per 1000 person-years (83 of 18,895 users [0.44%]) and 9.5 per 1000 person-years (85 of 18,895 [0.45%]), respectively. The adjusted hazard ratio was 0.92 (95% CI 0.68 to 1.26). The incidence rate among users of ARBs was 15.8 per 1000 person-years (79 out of 10,623 users [0.74%]). The adjusted hazard ratio was 1.38 (95% CI 0.98 to 1.95). There were no significant associations between use of RAS inhibitors and all-cause mortality. Conclusion Use of ACE inhibitors was not associated with the risk of COVID-19 whereas use of ARBs was associated with a statistically non-significant increase compared to the use of CCBs. However, no significant associations were observed between prescription of either ACE inhibitors or ARBs and all-cause mortality.