Evidence map›Paper›PMID 30446768›Full record

ReviewPediatric research2019

Neuroinflammation in preterm babies and autism spectrum disorders.

Cindy Bokobza, Juliette Van Steenwinckel, Shyamala Mani, Valérie Mezger, Bobbi Fleiss, Pierre Gressens

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Pediatric research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
11.6field-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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 99 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Prematurity and autism: a dose-response relationship across gestational age.Journal of perinatology : official journal of the California Perinatal Association · 2026
    Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Antioxidant-Effective Quercetin Through Modulation of Brain Interleukin-13 Mitigates Autistic-Like Behaviors in the Propionic Acid-Induced Autism Model in Rats.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
    Article
  19. Review
  20. Article
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

6 authors at 5 institutions in 2 countries.

Cindy BokobzaPROTECT, INSERM, Université Paris Diderot, Sorbonne Paris Cité, 75019, Paris, France.
Juliette Van SteenwinckelPROTECT, INSERM, Université Paris Diderot, Sorbonne Paris Cité, 75019, Paris, France.
Shyamala ManiCuradev Pharma Pvt. Ltd, Noida, India.
Valérie MezgerCNRS, UMR7216 Épigénétique et Destin Cellulaire, 75205, Paris 13, France.
Bobbi FleissSchool of Health and Biomedical Sciences, RMIT University, Bundoora, VIC, Australia.
Pierre GressensPROTECT, INSERM, Université Paris Diderot, Sorbonne Paris Cité, 75019, Paris, France. pierre.gressens@inserm.fr.
Epigénétique et Destin Cellulaire · FRInserm · FRRMIT University · AUSorbonne Paris Cité · FRUniversité Paris Cité · FR

Funding

Department of Health
6 · The paper itself

Abstract

Genetic anomalies have a role in autism spectrum disorders (ASD). Each genetic factor is responsible for a small fraction of cases. Environment factors, like preterm delivery, have an important role in ASD. Preterm infants have a 10-fold higher risk of developing ASD. Preterm birth is often associated with maternal/fetal inflammation, leading to a fetal/neonatal inflammatory syndrome. There are demonstrated experimental links between fetal inflammation and the later development of behavioral symptoms consistent with ASD. Preterm infants have deficits in connectivity. Most ASD genes encode synaptic proteins, suggesting that ASD are connectivity pathologies. Microglia are essential for normal synaptogenesis. Microglia are diverted from homeostatic functions towards inflammatory phenotypes during perinatal inflammation, impairing synaptogenesis. Preterm infants with ASD have a different phenotype from term born peers. Our original hypothesis is that exposure to inflammation in preterm infants, combined with at risk genetic background, deregulates brain development leading to ASD.

Indexed as

Infant, PrematureAutism Spectrum DisorderCentral Nervous System DiseasesHumansInfant, NewbornInflammation

Identifiers

PMID30446768
OpenAlexW2901370444

What OpenQuestion holds

Textmetadata
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.