Evidence map›Paper›PMID 42369668›Full record

ReviewJournal of cardiovascular and thoracic research2026

ACE/ACE2 axis in cardiovascular disease and COVID-19: Molecular insights and therapeutic perspectives.

Sony Peter, Thiruchenduran Mohana, Dhanavel Anandhi, Vishwanathan Sathya Priya, Romi Keerikkattil Sleeba, Harisree Panikkaveedu Haridas, Midhun Thazhissery Mohanan, Swathi Thoduvayil, Sinha Mathew, Dhanya Muraleedharan Santhamma and 1 more

Abstract readReview
In one paragraph

Review in Journal of cardiovascular and thoracic research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Sony PeterMeenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.ORCID https://orcid.org/0000-0001-8647-8766
Thiruchenduran MohanaDepartment of Biochemistry, Meenakshi Ammal Dental College & Hospital, Meenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.ORCID https://orcid.org/0009-0002-2113-2515
Dhanavel AnandhiMeenakshi Ammal Dental College & Hospital, Meenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.
Vishwanathan Sathya PriyaDepartment of Biochemistry, ACS Medical College & Hospital, Chennai, Tamil Nadu, India.
Romi Keerikkattil SleebaMeenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.
Harisree Panikkaveedu HaridasMeenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.
Midhun Thazhissery MohananMeenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.
Swathi ThoduvayilMeenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.
Sinha MathewMeenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.
Dhanya Muraleedharan SanthammaMeenakshi Academy of Higher Education and Research (Deemed to be University), Chennai, Tamil Nadu, India.
Dinesh Roy DivakaranCentre for Advanced Genetic Studies, Thiruvananthapuram, Kerala, India.ORCID https://orcid.org/0009-0005-7124-148X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The renin-angiotensin system (RAS) plays a central role in regulating blood pressure and cardiovascular health. Angiotensin-converting enzyme (ACE) facilitates the conversion of angiotensin I to angiotensin II, a potent vasoconstrictor that contributes to hypertension and heart failure. Conversely, ACE2 converts angiotensin II into angiotensin-(1-7), a vasodilator with protective cardiovascular effects. An imbalance between ACE and ACE2 activities has been increasingly associated with the progression of cardiovascular diseases and complications related to COVID-19. This review analyzed 100 relevant studies published up to May 2024, identified through a comprehensive literature search on PubMed and Scopus. The findings highlighted that dysregulation of the ACE/ACE2 axis exacerbates cardiovascular dysfunction. The interaction of SARS-CoV-2 with ACE2 reduces its protective function, intensifying inflammatory responses and leading to complications such as lung injury and heart failure. Additionally, genetic polymorphisms in ACE and ACE2 influence individual susceptibility and severity of COVID-19. Promising therapeutic strategies, including ACE2-based peptides and angiotensin II receptor modulators, are under investigation but require further clinical validation. Targeting the ACE/ACE2 axis could provide effective treatment options for cardiovascular disease and COVID-19-related complications, warranting further in-depth research.

Indexed as

Angiotensin-(1-7)Angiotensin-converting enzymeCOVID-19Heart failureMyocardial tissueRenin-angiotensin system

Identifiers

PMID42369668
PMCPMC13309327

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.