Evidence map›Paper›PMID 36994431›Full record

ReviewFrontiers in pediatrics2023

The role of interleukin-1 in perinatal inflammation and its impact on transitional circulation.

Josephine C Owen, Steven P Garrick, Briana M Peterson, Philip J Berger, Marcel F Nold, Arvind Sehgal, Claudia A Nold-Petry

Open access · goldFull text readReview
In one paragraph

Review in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
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  11. Effects of multiple pro-inflammatory stimuliFrontiers in immunology · 2023
    Article
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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

7 authors at 3 institutions in 1 country.

Josephine C OwenRitchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
Steven P GarrickRitchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
Briana M PetersonRitchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
Philip J BergerRitchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
Marcel F NoldRitchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
Arvind SehgalDepartment of Paediatrics, Monash University, Melbourne, VIC, Australia.
Claudia A Nold-PetryRitchie Centre, Hudson Institute of Medical Research, Melbourne, VIC, Australia.
Hudson Institute of Medical Research · AUMonash Children’s Hospital · AUMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Preterm birth is defined as delivery at <37 weeks of gestational age (GA) and exposes 15 million infants worldwide to serious early life diseases. Lowering the age of viability to 22 weeks GA entailed provision of intensive care to a greater number of extremely premature infants. Moreover, improved survival, especially at extremes of prematurity, comes with a rising incidence of early life diseases with short- and long-term sequelae. The transition from fetal to neonatal circulation is a substantial and complex physiologic adaptation, which normally happens rapidly and in an orderly sequence. Maternal chorioamnionitis or fetal growth restriction (FGR) are two common causes of preterm birth that are associated with impaired circulatory transition. Among many cytokines contributing to the pathogenesis of chorioamnionitis-related perinatal inflammatory diseases, the potent pro-inflammatory interleukin (IL)-1 has been shown to play a central role. The effects of utero-placental insufficiency-related FGR and in-utero hypoxia may also be mediated, in part, via the inflammatory cascade. In preclinical studies, blocking such inflammation, early and effectively, holds great promise for improving the transition of circulation. In this mini-review, we outline the mechanistic pathways leading to abnormalities in transitional circulation in chorioamnionitis and FGR. In addition, we explore the therapeutic potential of targeting IL-1 and its influence on perinatal transition in the context of chorioamnionitis and FGR.

Indexed as

chorioamnionitisfetal growth restrictioninterleukin-1perinatal inflammationtransitional circulation

Identifiers

PMID36994431
PMCPMC10040554
OpenAlexW4324085839

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read11
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.