Evidence map›Paper›PMID 32853537›Full record

ArticleAmerican journal of obstetrics and gynecology2021

Expression of severe acute respiratory syndrome coronavirus 2 cell entry genes, angiotensin-converting enzyme 2 and transmembrane protease serine 2, in the placenta across gestation and at the maternal-fetal interface in pregnancies complicated by preterm birth or preeclampsia.

Enrrico Bloise, Jianhong Zhang, Jittanan Nakpu, Hirotaka Hamada, Caroline E Dunk, Siliang Li, Guinever E Imperio, Lubna Nadeem, Mark Kibschull, Phetcharawan Lye and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of obstetrics and gynecology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 4 pooled it
8.4field-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

64 citing papers in PubMed, 4 syntheses or guidelines pooled it, 101 citations in OpenAlex.

  1. COVID-19 and Preeclampsia: A Systematic Review of Pathophysiological Interactions.Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia · 2023
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  20. Coronavirus Disease-2019 in Pregnancy.Clinics in chest medicine · 2023
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4 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 2 countries.

Enrrico BloiseDepartment of Morphology, Federal University of Minas Gerais, Belo Horizonte, Brazil; Department of Physiology, University of Toronto, Toronto, Ontario, Canada. Electronic address: ebloise@icb.ufmg.br.
Jianhong ZhangLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Jittanan NakpuLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Hirotaka HamadaDepartment of Physiology, University of Toronto, Toronto, Ontario, Canada.
Caroline E DunkLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Siliang LiLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Guinever E ImperioLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Lubna NadeemLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Mark KibschullLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada.
Phetcharawan LyeDepartment of Physiology, University of Toronto, Toronto, Ontario, Canada.
Stephen G MatthewsLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada; Department of Physiology, University of Toronto, Toronto, Ontario, Canada; Departments of Obstetrics and Gynecology and Medicine, University of Toronto, Toronto, Ontario, Canada.
Stephen J LyeLunenfeld-Tanenbaum Research Institute, Sinai Health System, Toronto, Ontario, Canada; Department of Physiology, University of Toronto, Toronto, Ontario, Canada; Departments of Obstetrics and Gynecology and Medicine, University of Toronto, Toronto, Ontario, Canada.
Lunenfeld-Tanenbaum Research Institute · CAUniversity of Toronto · CAUniversidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough there is some evidence that severe acute respiratory syndrome coronavirus 2 can invade the human placenta, limited data exist on the gestational age-dependent expression profile of the severe acute respiratory syndrome coronavirus 2 cell entry mediators, angiotensin-converting enzyme 2 and transmembrane protease serine 2, at the human maternal-fetal interface. There is also no information as to whether the expression of these mediators is altered in pregnancies complicated by preeclampsia or preterm birth. This is important because the expression of decidual and placental angiotensin-converting enzyme 2 and transmembrane protease serine 2 across gestation may affect the susceptibility of pregnancies to vertical transmission of severe acute respiratory syndrome coronavirus 2.

objectiveThis study aimed to investigate the expression pattern of specific severe acute respiratory syndrome coronavirus 2 cell entry genes, angiotensin-converting enzyme 2 and transmembrane protease serine 2, in the placenta across human pregnancy and in paired samples of decidua and placenta in pregnancies complicated by preterm birth or preeclampsia compared with those in term uncomplicated pregnancies. STUDY

designIn this study, 2 separate cohorts of patients, totaling 87 pregnancies, were included. The first cohort was composed of placentae from first- (7-9 weeks), second- (16-18 weeks), and third-trimester preterm (26-31 weeks) and third-trimester term (38-41 weeks) pregnancies (n=5/group), whereas the second independent cohort included matched decidua and placentae from pregnancies from term uncomplicated pregnancies (37-41 weeks' gestation; n=14) and pregnancies complicated by preterm birth (26-37 weeks' gestation; n=11) or preeclampsia (25-37 weeks' gestation; n=42). Samples were subjected to quantitative polymerase chain reaction and next-generation sequencing or RNA sequencing for next-generation RNA sequencing for angiotensin-converting enzyme 2 and transmembrane protease serine 2 mRNA expression quantification, respectively.

resultsIn the first cohort, angiotensin-converting enzyme 2 and transmembrane protease serine 2, exhibited a gestational age-dependent expression profile, that is, angiotensin-converting enzyme 2 and transmembrane protease serine 2 mRNA was higher (P<.05) in the first-trimester placenta than in second-trimester, preterm birth, and term placentae (P<.05) and exhibited a negative correlation with gestational age (P<.05). In the second cohort, RNA sequencing demonstrated very low or undetectable expression levels of angiotensin-converting enzyme 2 in preterm birth, preeclampsia, and term decidua and in placentae from late gestation. In contrast, transmembrane protease serine 2 was expressed in both decidual and placental samples but did not change in pregnancies complicated by either preterm birth or preeclampsia.

conclusionThe increased expression of these severe acute respiratory syndrome coronavirus 2 cell entry-associated genes in the placenta in the first trimester of pregnancy compared with those in later stages of pregnancy suggests the possibility of differential susceptibility to placental entry to severe acute respiratory syndrome coronavirus 2 across pregnancy. Even though there is some evidence of increased rates of preterm birth associated with severe acute respiratory syndrome coronavirus 2 infection, we found no increase in mRNA expression of angiotensin-converting enzyme 2 or transmembrane protease serine 2 at the maternal-fetal interface.

Indexed as

Angiotensin-Converting Enzyme 2COVID-19FemaleHumansPlacentaPre-EclampsiaPregnancyPremature BirthRNA, MessengerSARS-CoV-2Serine EndopeptidasesVirus InternalizationACE2 protein, humanAngiotensin-Converting Enzyme 2RNA, MessengerSerine EndopeptidasesTMPRSS2 protein, humanangiotensin-converting enzyme 2coronavirus disease 2019deciduagestation age–dependent gene expressionplacentapreeclampsiapreterm birthsevere acute respiratory syndrome coronavirus 2term pregnancies

Identifiers

PMID32853537
PMCPMC7445125
OpenAlexW3080259982

What OpenQuestion holds

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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 OpenQuestion graph.