The Effect of RAAS Blockers on ACE2 Levels
Study Details
Study Description
Brief Summary
Blockage of renin-angiotensin-aldosterone system (RAAS) by angiotensin converting enzyme inhibitors (ACEI) and angiotensin receptor blockers (ARBs) is considered the first-choice of drugs for treatment of hypertension, heart failure and chronic kidney disease (Ma, Kam et al. 2010). However, the interplay between RAAS blockers and ACE2 hasn't been fully elucidated (Vaduganathan, Vardeny et al. 2020).
SARS-CoV-2 is thought to infect host cells through ACE2 to cause coronavirus disease 2019 (COVID-19). Recent studies revealed that the spikes of COVID-19 could bind to the surface receptors of sensitive cells after contacting the airway surface, which may mediate virus entry into target cells and viral replication, and ACE2 might be a mediator of infection (South, Brady et al. 2020). Therefore, the imbalance in the RAAS, with a shift towards ACE/Ang II and suppression of ACE2/Ang-(1-7), may be an important mediator of COVID-19. To date, conflicting evidences were reported linking the use of RAAS blockers and the susceptibility to the virus. However, others showed that treatment with an RAAS blockers may downregulate the expression of ACE2 but have no significant effect on its activity (Li, Hu et al. 2020). This research importantly aimed to solve this important issue by determining the exact association between ARBs and ACE inhibitor and ACE2 activity and levels on clinical and experimental prospects.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
Blockage of renin-angiotensin-aldosterone system (RAAS) by angiotensin converting enzyme inhibitors (ACEI) and angiotensin receptor blockers (ARBs) is considered the first-choice of drugs for treatment of hypertension, heart failure and chronic kidney disease (Ma, Kam et al. 2010). The classic RAAS primarily involves 2 enzymes: renin, which cleaves angiotensinogen to the inactive decapeptide angiotensin (Ang) I; and ACE that hydrolyzes Ang I to the octapeptide Ang II, the well-known vasopressor agent (Farag, Maheshwari et al. 2015). In fact, the enzymatic cascade of the RAS encompasses an ACE homolog known as ACE2. Whereas, the ACE2-dependent pathways directly yield Ang (1-9) from Ang I and degrade Ang II to Ang (1-7), which is vasodilator and acts as a feedback mechanism to antagonize the vasopressor effect of Ang II (Jiang, Yang et al. 2014). Indeed, ACE inhibitors effectively attenuate Ang II formation and augment the levels of the heptapeptide Ang (1-7) (Padda, Shi et al. 2015). However, the interplay between RAAS blockers and ACE2 hasn't been fully elucidated (Vaduganathan, Vardeny et al. 2020).
SARS-CoV-2 is thought to infect host cells through ACE2 to cause coronavirus disease 2019 (COVID-19). Recent studies revealed that the spikes of COVID-19 could bind to the surface receptors of sensitive cells after contacting the airway surface, which may mediate virus entry into target cells and viral replication, and ACE2 might be a mediator of infection (South, Brady et al. 2020). Therefore, the imbalance in the RAAS, with a shift towards ACE/Ang II and suppression of ACE2/Ang-(1-7), may be an important mediator of COVID-19. To date, conflicting evidences were reported linking the use of RAAS blockers and the susceptibility to the virus. However, others showed that treatment with an RAAS blockers may downregulate the expression of ACE2 but have no significant effect on its activity (Li, Hu et al. 2020).
Furthermore, SARS-CoV-2 infection has largely been influenced by multiorgan involvement inducing multiple comorbidities due to the wide distribution of ACE2 thought out the whole body (Zaim, Chong et al. 2020). In addition, hypertension, cardiovascular disease, and chronic kidney disease are supposed to be potential but unconfirmed risk factors for COVID-19 in adults and children (Tadic, Cuspidi et al. 2020). However, the expression of ACE2 may be lower in patients with hypertension than in people with normal blood pressure (Li, Hu et al. 2020). Concluding more conflicting evidences for the association of COVID-19 with RAAS inhibitors.
Given the RAAS importance to cardiovascular and kidney physiology, and the association between chronic diseases and COVID-19, could shed light on potential relationships between ACE inhibitor and ARB use and COVID-19 (Wang, Edin et al. 2020).
Accordingly, evidences are required to solve the question of whether ARBs and ACE inhibitor have either favorable or harmful effects on the susceptibility to SARS-CoV-2 in addition to the severity and outcomes of COVID-19 infection. This research importantly aimed to solve this important issue by determining the exact association between ARBs and ACE inhibitor and ACE2 activity and levels on clinical and experimental prospects.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| ACEIs group Patients suffer from cardiovascular diseases)controlled hypertension or heart failure ) taking ACE inhibitors |
Drug: ACE inhibitor ,angiotensin receptor blockers
patients taking ACEI or ARBs with cardiovascular disease
|
| ARBs group Patients suffer from cardiovascular diseases)controlled hypertension or heart failure ) taking Angiotensin receptor blockers |
Drug: ACE inhibitor ,angiotensin receptor blockers
patients taking ACEI or ARBs with cardiovascular disease
|
| healthy matched healthy controls |
Outcome Measures
Primary Outcome Measures
- Effect of RAAS blockers on ACE2 levels [at least 6 months]
ACE2 levels in cardiovascular disease patients
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Patients age> 18 years
-
Taking ACE II inhibitors or angiotensin II blockers (according to maximum tolerated dose specified by guidelines)
-
History of essential hypertension or heart failure
Exclusion Criteria:
-
patients who suffer from secondary hypertension, including idiopathic hyperaldosteronism, renal artery stenosis
-
Patient reported history of severe liver disease
-
a history or suspicion of alcohol or drug abuse; and mental illness
-
Pregnant and breast feeding
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Ainshams University | Cairo | Select A State Or Province | Egypt | 02 |
Sponsors and Collaborators
- Ain Shams University
Investigators
- Principal Investigator: ebtehal el demerdash, prof, Ain Shams University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- FAMASU/2021