Evidence map›Paper›PMID 36298762›Full record

ArticleViruses2022

Imbalanced Angiogenesis in Pregnancies Complicated by SARS-CoV-2 Infection.

Valentina Giardini, Sara Ornaghi, Carlo Gambacorti-Passerini, Marco Casati, Andrea Carrer, Eleonora Acampora, Maria Viola Vasarri, Francesca Arienti, Patrizia Vergani

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Pregnancy and COVID-19.Journal of clinical medicine · 2022
    Review
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

9 authors at 1 institution in 1 country.

Valentina GiardiniDepartment of Obstetrics and Gynecology, MBBM Foundation Onlus, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.ORCID 0000-0002-6010-9994
Sara OrnaghiDepartment of Obstetrics and Gynecology, MBBM Foundation Onlus, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.ORCID 0000-0001-6898-7217
Carlo Gambacorti-PasseriniHematology Division, ASST-Monza, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.
Marco CasatiLaboratory Medicine, ASST-Monza, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.ORCID 0000-0002-4968-1455
Andrea CarrerHematology Division, ASST-Monza, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.
Eleonora AcamporaDepartment of Obstetrics and Gynecology, MBBM Foundation Onlus, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.
Maria Viola VasarriDepartment of Obstetrics and Gynecology, MBBM Foundation Onlus, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.ORCID 0000-0002-9170-901X
Francesca ArientiDepartment of Obstetrics and Gynecology, MBBM Foundation Onlus, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.
Patrizia VerganiDepartment of Obstetrics and Gynecology, MBBM Foundation Onlus, San Gerardo Hospital, University of Milano-Bicocca, 20900 Monza, Italy.ORCID 0000-0001-5028-0045
University of Milano-Bicocca · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 and preeclampsia (preE) share the ANG-II mediated endothelial dysfunction, resulting from a significant dysregulation of RAS and an imbalanced proportion of anti-angiogenic and pro-angiogenic soluble plasmatic factors. Of note, an increased incidence of preE has been reported among COVID-19-infected mothers compared to the general pregnant population. The two most promising angiogenic markers are the soluble fms-like tyrosine kinase receptor-1 (sFlt-1), the major antiangiogenic factor, and the placental growth factor (PlGF), a powerful angiogenic factor. Since these markers have proven useful in the prediction, diagnosis, and severity of preE, this study aimed to evaluate their maternal serum levels in pregnancies complicated by SARS-CoV-2 infection and to assess their potential use to guide the management of these women. A retrospective analysis of SARS-CoV-2-positive pregnant women was performed. The serum levels of sFlt-1 and PlGF were collected at the diagnosis of SARS-CoV-2 infection at the hospital, before the beginning of steroid/hydroxychloroquine and/or antithrombotic therapy. The sFlt-1/PlGF ratio was stratified using cut-off values clinically utilized in the diagnosis and prediction of preE (low < 38, intermediate 38−85/110* and high >85/110*, * if before or after the 34th week of gestation). A total of 57 women were included, of whom 20 (35%) had signs and symptoms of COVID-19 at hospital presentation and 37 (65%) were asymptomatic. None were vaccinated. The mean gestational age at diagnosis of SARS-CoV-2 infection was 32 weeks in symptomatic patients and 37 weeks and 5 days in asymptomatic ones (p = 0.089). sFlt-1 serum levels were higher in SARS-CoV-2 positive asymptomatic patients compared to women with COVID-19 related symptoms (4899 ± 4357 pg/mL vs. 3187 ± 2426 pg/mL, p = 0.005). sFlt-1/PlGF at admission was <38 in 18 of the 20 symptomatic women (90%) compared to 22 (59%) of the asymptomatic patients (p = 0.018). Of note, two of the three women admitted to the intensive care unit had a very low ratio (<2). In turn, rates of patients with sFlt-1/PlGF at admission > 85/110 were not significantly different between the two groups: 11% in asymptomatic patients (4/37) vs. none of the symptomatic patients (p = 0.286), and all of them presented a placental dysfunction, like preE (n = 1) and FGR (n = 3). Of note, there were no stillbirths or maternal or neonatal deaths among symptomatic patients; also, no cases of preE, FGR, or small for gestational age neonates were diagnosed. In conclusion, our data suggest that SARS-CoV-2 infection during pregnancy could influence the angiogenic balance. A significant pathological alteration of the sFlt-1/PlGF ratio cannot be identified during the symptomatic phase; however, if left untreated, SARS-CoV-2 infection could potentially trigger placental dysfunction.

Indexed as

COVID-19Pre-EclampsiaAngiogenesis Inducing AgentsBiomarkersFemaleFibrinolytic AgentsHumansHydroxychloroquineInfant, NewbornPlacentaPlacenta Growth FactorPregnancyRetrospective StudiesSARS-CoV-2StillbirthVascular Endothelial Growth Factor Receptor-1Angiogenesis Inducing AgentsBiomarkersFibrinolytic AgentsHydroxychloroquinePlacenta Growth FactorVascular Endothelial Growth Factor Receptor-1angiogenic factorsCOVID-19endothelial dysfunctionplacental dysfunctionpreeclampsiaSARS-CoV-2sFlt-1

Identifiers

PMID36298762
PMCPMC9610426
OpenAlexW4304787237

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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.