Evidence map›Paper›PMID 34970270›Full record

ReviewFrontiers in immunology2021

Acute Atherosis Lesions at the Fetal-Maternal Border: Current Knowledge and Implications for Maternal Cardiovascular Health.

Daniel Pitz Jacobsen, Heidi Elisabeth Fjeldstad, Guro Mørk Johnsen, Ingrid Knutsdotter Fosheim, Kjartan Moe, Patji Alnæs-Katjavivi, Ralf Dechend, Meryam Sugulle, Anne Cathrine Staff

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 33 citations in OpenAlex.

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  12. Placental syndromes and maternal cardiovascular health.Clinical science (London, England : 1979) · 2023
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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

9 authors at 3 institutions in 2 countries.

Daniel Pitz JacobsenDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Heidi Elisabeth FjeldstadDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Guro Mørk JohnsenDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Ingrid Knutsdotter FosheimDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Kjartan MoeDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Patji Alnæs-KatjaviviDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Ralf DechendExperimental and Clinical Research Center, A Cooperation of Charité-Universitätsmedizin Berlin and Max-Delbruck Center for Molecular Medicine, Berlin, Germany.
Meryam SugulleDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Anne Cathrine StaffDivision of Obstetrics and Gynaecology, Oslo University Hospital, Oslo, Norway.
Oslo University Hospital · NOCharité - Universitätsmedizin Berlin · DEUniversity of Oslo · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Decidua basalis, the endometrium of pregnancy, is an important interface between maternal and fetal tissues, made up of both maternal and fetal cells. Acute atherosis is a uteroplacental spiral artery lesion. These patchy arterial wall lesions containing foam cells are predominantly found in the decidua basalis, at the tips of the maternal arteries, where they feed into the placental intervillous space. Acute atherosis is prevalent in preeclampsia and other obstetric syndromes such as fetal growth restriction. Causal factors and effects of acute atherosis remain uncertain. This is in part because decidua basalis is challenging to sample systematically and in large amounts following delivery. We summarize our decidua basalis vacuum suction method, which facilitates tissue-based studies of acute atherosis. We also describe our evidence-based research definition of acute atherosis. Here, we comprehensively review the existing literature on acute atherosis, its underlying mechanisms and possible short- and long-term effects. We propose that multiple pathways leading to decidual vascular inflammation may promote acute atherosis formation, with or without poor spiral artery remodeling and/or preeclampsia. These include maternal alloreactivity, ischemia-reperfusion injury, preexisting systemic inflammation, and microbial infection. The concept of acute atherosis as an inflammatory lesion is not novel. The lesions themselves have an inflammatory phenotype and resemble other arterial lesions of more extensively studied etiology. We discuss findings of concurrently dysregulated proteins involved in immune regulation and cardiovascular function in women with acute atherosis. We also propose a novel hypothesis linking cellular fetal microchimerism, which is prevalent in women with preeclampsia, with acute atherosis in pregnancy and future cardiovascular and neurovascular disease. Finally, women with a history of preeclampsia have an increased risk of premature cardiovascular disease. We review whether presence of acute atherosis may identify women at especially high risk for premature cardiovascular disease.

Indexed as

Disease SusceptibilityArteriesAtherosclerosisBiomarkersBiopsyCardiovascular DiseasesDeciduaEndometritisFemaleHumansImmunohistochemistryIsoantigensOrgan SpecificityPlacentaPostpartum PeriodPregnancyBiomarkersIsoantigensacute atherosiscardiovascular diseasedecidua basalisinflammationmicrochimerismplacentapreeclampsiatolerance

Identifiers

PMID34970270
PMCPMC8712939
OpenAlexW4200324095

What OpenQuestion 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 OpenQuestion graph.