Evidence map›Paper›PMID 34338772›Full record

ReviewClinical science (London, England : 1979)2021

Role of ACE2 in pregnancy and potential implications for COVID-19 susceptibility.

Nayara Azinheira Nobrega Cruz, Danielle Stoll, Dulce Elena Casarini, Mariane Bertagnolli

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical science (London, England : 1979), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 3 pooled it
8.9field-weighted citation impact, top 2% of its field
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

30 citing papers in PubMed, 3 syntheses or guidelines pooled it, 62 citations in OpenAlex.

  1. Pooled it
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  6. Association ofViruses · 2024
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  16. Maternal deaths caused by eclampsia in Brazil: a descriptive study from 2000 to 2021.Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia · 2024
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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

4 authors at 2 institutions in 2 countries.

Nayara Azinheira Nobrega CruzDepartment of Medicine, Discipline of Nephrology, Federal University of Sao Paulo, São Paulo, Brazil.ORCID 0000-0002-9689-9545
Danielle StollDepartment of Medicine, Discipline of Nephrology, Federal University of Sao Paulo, São Paulo, Brazil.
Dulce Elena CasariniDepartment of Medicine, Discipline of Nephrology, Federal University of Sao Paulo, São Paulo, Brazil.ORCID 0000-0003-1912-4292
Mariane BertagnolliResearch Center of the Hospital Sacré-Coeur, CIUSSS Nord-de-l'Île-de-Montréal, Montréal, Canada.ORCID 0000-0002-1093-1445
Centre Intégré Universitaire de Santé et de Services Sociaux du Saguenay–Lac-Saint-Jean · CAUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In times of coronavirus disease 2019 (COVID-19), the impact of severe acute respiratory syndrome (SARS)-coronavirus (CoV)-2 infection on pregnancy is still unclear. The presence of angiotensin-converting enzyme (ACE) 2 (ACE2), the main receptor for SARS-CoV-2, in human placentas indicates that this organ can be vulnerable for viral infection during pregnancy. However, for this to happen, additional molecular processes are critical to allow viral entry in cells, its replication and disease manifestation, particularly in the placenta and/or feto-maternal circulation. Beyond the risk of vertical transmission, COVID-19 is also proposed to deplete ACE2 protein and its biological actions in the placenta. It is postulated that such effects may impair essential processes during placentation and maternal hemodynamic adaptations in COVID-19 pregnancy, features also observed in several disorders of pregnancy. This review gathers information indicating risks and protective features related to ACE2 changes in COVID-19 pregnancies. First, we describe the mechanisms of SARS-CoV-2 infection having ACE2 as a main entry door and current evidence of viral infection in the placenta. Further, we discuss the central role of ACE2 in physiological systems such as the renin-angiotensin system (RAS) and the kallikrein-kinin system (KKS), both active during placentation and hemodynamic adaptations of pregnancy. Significant knowledge gaps are also identified and should be urgently filled to better understand the fate of ACE2 in COVID-19 pregnancies and the potential associated risks. Emerging knowledge will be able to improve the early stratification of high-risk pregnancies with COVID-19 exposure as well as to guide better management and follow-up of these mothers and their children.

Indexed as

Angiotensin-Converting Enzyme 2BiomarkersCOVID-19FemaleHumansInfectious Disease Transmission, VerticalPlacentaPregnancyPregnancy Complications, InfectiousReceptors, CoronavirusRisk FactorsSARS-CoV-2Virus InternalizationACE2 protein, humanAngiotensin-Converting Enzyme 2BiomarkersReceptors, Coronavirusangiotensin converting enzyme 2cardiovascular diseaseCOVID-19placental biologypregnancySARS-COV-2

Identifiers

PMID34338772
PMCPMC8329853
OpenAlexW3192802616

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.