Abstract
The review article summarizes the world’s research on the effect of angiotensin II receptor blockers and statins on the frequency of severe course, hospitalization, development of complications and mortality from SARS-CoV-2 in patients at risk by age and concomitant diseases. Given the extremely wide range of antihypertensive, anti-ischemic, and other cardiac medications that patients take for a long time before and during SARS-CoV-2, the search for optimal remedies remains difficult, and the amount of relevant data has long been insufficient to draw even preliminary conclusions. Some of the most common antihypertensive medications are angiotensin II receptor blockers. According to current data, it is recommended to continue taking these drugs in patients with COVID-19 who are already on such therapy, until acute contraindications occur. Other common medications that can prevent and slow endothelial damage are statins used for lipidlowering purposes in patients with atherosclerosis. In addition to direct protective effects on the vascular endothelium, statins have a number of characteristics that suggest their ability to prevent pathological processes characteristic of severe and very severe COVID-19: cytokine storm and vascular microthrombosis.
References
2. Cdc, COVID-response team: preliminary estimates of the prevalence of selected underlying health conditions among patients with coronavirus disease 2019 — United States, february 12-march 28, 2020, MMWR Morb. Mortal. Wkly. Rep. 69 (2020). — Р. 382-386.
3. Wu C., Chen X., Cai Y., et al. Risk factors associated with acute respiratory distress syndrome and death in patients with coronavirus disease 2019 pneumonia in wuhan, China // JAMA Intern. Med. — 2020. — Vol. 180. — P. 934-943.
4. Zhou F., Yu T., Du R., et al. Clinical course and risk factors for mortality of adult inpatients with COVID‑19 in Wuhan, China: a retrospective cohort study // Lancet. — 2020. — Vol. 395. — P. 1054-1062.
5. Guo T., Fan Y., Chen M., et al. Cardiovascular implications of fatal outcomes of patients with coronavirus disease 2019 (COVID‑19) // JAMA Cardiol. — 2020. — Vol. 5. — P. 811-818.
6. Brunner H., Cockcroft J.R., Deanfield J., et al. Endothelial function and dysfunction. Part II: association with cardiovascular risk factors and diseases. a statement by the working group on endothelins and endothelial factors of the European society of hypertension // J. Hypertens. — 2005. — Vol. 23. — P. 233-246.
7. Vascular consequences of inflammation: a position statement from the ESH Working Group on Vascular Structure and Function and the ARTERY Society // Journal of Hypertension. — 2020. — Vol. 38 (9). — P. 1682-1698. doi: 10.1097/HJH.0000000000002508.
8. N¨agele M.P., Barthelmes J., Ludovici V., et al. Retinal microvascular dysfunction in heart failure // Eur. Heart J. — 2018. — Vol. 39. — P. 47-56.
9. Santos R.A.S., Sampaio W.O., Alzamora A.C., et al. The ACE2/angiotensin-(1-7)/ MAS Axis of the renin-angiotensin system: focus on angiotensin-(1-7) // Physiol. Rev. — 2018. — Vol. 98. — P. 505-553.
10. Verdecchia P., Cavallini C., Spanevello A., et al. The pivotal link between ACE2 deficiency and SARS-CoV‑2 infection // Eur. J. Intern. Med. — 2020. — Vol. 76. — P. 14-20.
11. Reynolds H.R., Adhikari S., Pulgarin C., et al. Renin-angiotensin-Aldosterone system inhibitors and risk of covid‑19 // N. Engl. J. Med. — 2020. — Vol. 382. — P. 2441-2448.
12. Shahin Y., Khan J.A., Samuel N., et al. Angiotensin converting enzyme inhibitors effect on endothelial dysfunction: a meta-analysis of randomised controlled trials // Atherosclerosis. — 2011. — Vol. 216. — P. 7-16.
13. Li S., Wu Y., Yu G., et al. Angiotensin II receptor blockers improve peripheral endothelial function: a meta-analysis of randomized controlled trials // PloS One. — 2014. — Vol. 9. — P. e90217.
14. Muller D.N., Mervaala E.M., Dechend R., et al. Angiotensin II (AT(1)) receptor blockade reduces vascular tissue factor in angiotensin II-induced cardiac vasculopathy // Am. J. Pathol. — 2000. — Vol. 157. — P. 111-122.
15. Sodhi C.P., Nguyen J., Yamaguchi Y., et al. A dynamic variation of pulmonary ACE2 is required to modulate neutrophilic inflammation in response to Pseudomonas aeruginosa lung infection in mice // J. Immunol. — 2019. — Vol. 203. — P. 3000-3012.