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Review
. 2024 May 27:11:1409723.
doi: 10.3389/fcvm.2024.1409723. eCollection 2024.

The possible mechanism and research progress of ACE2 involved in cardiovascular injury caused by COVID-19: a review

Affiliations
Review

The possible mechanism and research progress of ACE2 involved in cardiovascular injury caused by COVID-19: a review

Dan Luo et al. Front Cardiovasc Med. .

Abstract

ACE2 is the earliest receptor discovered to mediate the entry of SARS-CoV-2. In addition to the receptor, it also participates in complex pathological and physiological processes, including regulating the RAS system, apelin, KKS system, and immune system. In addition to affecting the respiratory system, viral infections also interact with cardiovascular diseases. SARS-CoV-2 can directly invade the cardiovascular system through ACE2; Similarly, cardiovascular diseases such as hypertension and coronary heart disease can affect ACE2 levels and exacerbate the disease, and ACE2 dysregulation may also be a potential mechanism for long-term acute sequelae of COVID-19. Since the SARS CoV-2 epidemic, many large population studies have tried to clarify the current focus of debate, that is, whether we should give COVID-19 patients ACEI and ARB drug treatment, but there is still no conclusive conclusion. We also discussed potential disease treatment options for ACE2 at present. Finally, we discussed the researchers' latest findings on ACE2 and their prospects for future research.

Keywords: ACE2; RAS system; SARS-CoV-2; cardiovascular diseases; therapy.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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References

    1. Crackower MA, Sarao R, Oudit GY, Yagil C, Kozieradzki I, Scanga SE, et al. Angiotensin-converting enzyme 2 is an essential regulator of heart function. Nature. (2002) 417(6891):822–8. 10.1038/nature00786 - DOI - PubMed
    1. Tregoning JS, Flight KE, Higham SL, Wang Z, Pierce BF. Progress of the COVID-19 vaccine effort: viruses, vaccines and variants versus efficacy, effectiveness and escape. Nat Rev Immunol. (2021) 21(10):626–36. 10.1038/s41577-021-00592-1 - DOI - PMC - PubMed
    1. Oudit GY, Wang K, Viveiros A, Kellner MJ, Penninger JM. Angiotensin-converting enzyme 2-at the heart of the COVID-19 pandemic. Cell. (2023) 186(5):906–22. 10.1016/j.cell.2023.01.039 - DOI - PMC - PubMed
    1. Reynolds HR, Adhikari S, Pulgarin C, Troxel AB, Iturrate E, Johnson SB, et al. Renin-angiotensin-aldosterone system inhibitors and risk of COVID-19. N Engl J Med. (2020) 382(25):2441–8. 10.1056/NEJMoa2008975 - DOI - PMC - PubMed
    1. Zhang P, Zhu L, Cai J, Lei F, Qin J-J, Xie J, et al. Association of inpatient use of angiotensin-converting enzyme inhibitors and angiotensin II receptor blockers with mortality among patients with hypertension hospitalized with COVID-19. Circ Res. (2020) 126(12):1671–81. 10.1161/CIRCRESAHA.120.317134 - DOI - PMC - PubMed