Evidence map›Paper›PMID 35799507›Full record

ReviewNeural regeneration research2023

Interleukin-1: an important target for perinatal neuroprotection?

Sharmony B Kelly, Elys Green, Rod W Hunt, Claudia A Nold-Petry, Alistair J Gunn, Marcel F Nold, Robert Galinsky

Open access · goldAbstract readReview
In one paragraph

Review in Neural regeneration research, 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
12.6field-weighted citation impact, top 1% 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, 34 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Intra-amniotic infection withBrain communications · 2025
    Article
  9. Article
  10. Dopamine Activates the D1R-ZnCellular and molecular neurobiology · 2023
    Article
  11. Article
  12. The Role of the Interleukin-1 Family in Complications of Prematurity.International journal of molecular sciences · 2023
    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

7 authors at 4 institutions in 2 countries.

Sharmony B KellyThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne; Department of Obstetrics and Gynaecology, Monash University, Victoria, Australia.
Elys GreenDepartment of Pediatrics, Monash University, Victoria; Monash Newborn, Monash Children's Hospital, Melbourne, Australia.
Rod W HuntThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne; Department of Pediatrics, Monash University, Victoria; Monash Newborn, Monash Children's Hospital, Melbourne, Australia.
Claudia A Nold-PetryThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne; Department of Pediatrics, Monash University, Victoria, Australia.
Alistair J GunnDepartment of Physiology, The University of Auckland, Auckland, New Zealand.
Marcel F NoldThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne; Department of Pediatrics, Monash University, Victoria; Monash Newborn, Monash Children's Hospital, Melbourne, Australia.
Robert GalinskyThe Ritchie Centre, Hudson Institute of Medical Research, Melbourne; Department of Obstetrics and Gynaecology, Monash University, Victoria, Australia.
Monash University · AUHudson Institute of Medical Research · AUMonash Children’s Hospital · AUUniversity of Auckland · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perinatal inflammation is a significant risk factor for lifelong neurodevelopmental impairments such as cerebral palsy. Extensive clinical and preclinical evidence links the severity and pattern of perinatal inflammation to impaired maturation of white and grey matters and reduced brain growth. Multiple pathways are involved in the pathogenesis of perinatal inflammation. However, studies of human and experimental perinatal encephalopathy have demonstrated a strong causative link between perinatal encephalopathy and excessive production of the pro-inflammatory effector cytokine interleukin-1. In this review, we summarize clinical and preclinical evidence that underpins interleukin-1 as a critical factor in initiating and perpatuating systemic and central nervous system inflammation and subsequent perinatal brain injury. We also highlight the important role of endogenous interleukin-1 receptor antagonist in mitigating interleukin-1-driven neuroinflammation and tissue damage, and summarize outcomes from clinical and mechanistic animal studies that establish the commercially available interleukin-1 receptor antagonist, anakinra, as a safe and effective therapeutic intervention. We reflect on the evidence supporting clinical translation of interleukin-1 receptor antagonist for infants at the greatest risk of perinatal inflammation and impaired neurodevelopment, and suggest a path to advance interleukin-1 receptor antagonist along the translational path for perinatal neuroprotection.

Indexed as

braininflammationinterleukin-1interleukin-1 receptor antagonistinterleukin-1βneonatal encephalopathyneuroprotectionpreterm brain injury

Identifiers

PMID35799507
PMCPMC9241389
OpenAlexW4284963013

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.