Evidence map›Paper›PMID 42596967›Full record

ArticlePregnancy (Hoboken, N.J.)2025

Association between SARS-CoV-2 infection during pregnancy and placental pathology assessed by histology and gene expression.

Sunitha Suresh, Jessica L Britt, Alexa Freedman, Lauren Keenan-Devlin, Linda M Ernst, Whitney Lewandowski, Renee Odom-Konja, Lavisha Singh, Gregory E Miller, Steve Cole and 2 more

Abstract read
In one paragraph

Article in Pregnancy (Hoboken, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Sunitha SureshEndeavor Health Evanston Illinois USA.
Jessica L BrittPrisma Health Greenville North Carolina USA.
Alexa FreedmanEndeavor Health Evanston Illinois USA.
Lauren Keenan-DevlinEndeavor Health Evanston Illinois USA.
Linda M ErnstEndeavor Health Evanston Illinois USA.
Whitney LewandowskiEndeavor Health Evanston Illinois USA.
Renee Odom-KonjaEndeavor Health Evanston Illinois USA.
Lavisha SinghEndeavor Health Evanston Illinois USA.
Gregory E MillerNorthwestern University Evanston Illinois USA.
Steve ColeUniversity of California, Los Angeles Los Angeles California USA.
Amy H CrockettPrisma Health Greenville North Carolina USA.
Ann BordersEndeavor Health Evanston Illinois USA.

Funding

The impact of structural racism and discrimination on perinatal health during the COVID-19 pandemicR01HD092446 · NICHD · ENDEAVOR HEALTH CLINICAL OPERATIONS · PI BORDERS, ANN E.B., CROCKETT, AMY HAIRSTON · 2018 to 2022
$3.9M
Understanding socioeconomic disparities in perinatal risk: The role of epigenetic and transcriptional regulation in the placentaR01MD011749 · NIMHD · NORTHWESTERN UNIVERSITY · PI BORDERS, ANN E.B., MILLER, GREGORY EVAN · 2017 to 2021
$3.9M
NICHD NIH HHS R01 HD092446NIMHD NIH HHS R01 MD011749
6 · The paper itself

Abstract

Introduction: Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection during pregnancy has been associated with varying degrees of placental inflammation but the underlying molecular mechanism is unknown. We utilized placental gene expression analysis to examine possible mechanistic differences between patients with SARS-CoV-2 infection during pregnancy and uninfected controls. Methods: In this prospective dual-site cohort study, placentas were biopsied at delivery in patients infected with SARS-CoV-2 at different trimesters of pregnancy (case group). Specimens collected prior to the SARS-CoV-2 pandemic were utilized as controls. We examined differences in placental pathology based on four categories (acute inflammation, chronic inflammation, fetal vascular malperfusion, and maternal vascular malperfusion) by trimester of SARS-CoV-2 infection. Placental biopsies from the chorionic villous layer underwent gene expression analysis. Transcripts with more than twofold abundance difference between cases and controls were considered differentially expressed. Those differentially expressed transcripts were submitted to bioinformatic analysis to identify underlying cellular drivers and transcriptional pathways. All models were adjusted for study site, age, parity, body mass index, race/ethnicity, and insurance status. Results: Histology and gene expression were available for 886 historic control placentas. Seventy-one cases infected with SARS-CoV-2 were enrolled-70 placentas were analyzed for histology and 68 for gene expression. There was a higher frequency of high-grade pathology for patients infected in the first versus second/third trimester, 63.6% with any high-grade pathology for first trimester infection versus 28.8% in second to third trimester infection, Conclusion: SARS-CoV-2 infection was associated with multiple alterations in placental gene regulation, with increasing number of genes and transcription pathways differentially expressed with infection earlier in pregnancy. Future research should clarify the impact of these factors and how they ultimately result in placental pathology and obstetric outcomes.

Indexed as

gene expressionplacentaSARS‐COV‐2

Identifiers

PMID42596967
PMCPMC13344563

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.