Evidence map›Paper›PMID 30954546›Full record

ReviewFree radical biology & medicine2019

Oxygen radical disease in the newborn, revisited: Oxidative stress and disease in the newborn period.

Marta Perez, Mary E Robbins, Cecilie Revhaug, Ola D Saugstad

Abstract readReview
In one paragraph

Review in Free radical biology & medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed
15.9field-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

97 citing papers in PubMed, 195 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Antioxidant Effect of Melatonin in Preterm Newborns.Oxidative medicine and cellular longevity · 2021
    Trial
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Sex, hormones, and lung health.Physiological reviews · 2026
    Review
  14. Article
  15. Article
  16. Cannabidiol Protects the Neonatal Mouse Heart from Hyperoxia-Induced Injury.International journal of molecular sciences · 2025
    Article
  17. Article
  18. Review
  19. Article
  20. Article

37 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

4 authors at 4 institutions in 2 countries.

Marta PerezDivision of Neonatology, Stanley Manne Children's Research Institute, Ann and Robert H Lurie Children's Hospital, Chicago, IL, United States; Department of Pediatrics, Northwestern University, Feinberg School of Medicine, Chicago, IL, United States.
Mary E RobbinsDivision of Neonatology, Stanley Manne Children's Research Institute, Ann and Robert H Lurie Children's Hospital, Chicago, IL, United States; Department of Pediatrics, Northwestern University, Feinberg School of Medicine, Chicago, IL, United States.
Cecilie RevhaugDepartment of Pediatric Research, University of Oslo, Oslo University Hospital, Norway.
Ola D SaugstadDepartment of Pediatrics, Northwestern University, Feinberg School of Medicine, Chicago, IL, United States; Department of Pediatric Research, University of Oslo, Oslo University Hospital, Norway. Electronic address: odsaugstad@rr-research.no.
Lurie Children's Hospital · USNorthwestern University · USOslo University Hospital · NOUniversity of Oslo · NO

Funding

Mechanisms of Hydrocortisone Regulation of the Perinatal Pulmonary VasculatureK08HL124295 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI PEREZ, MARTA · 2017 to 2021
$817k
miR-17~92 Haploinsufficiency Influences Alveolar and Vascular Endothelial DevelopmentK08HL140152 · NHLBI · LURIE CHILDREN'S HOSPITAL OF CHICAGO · PI ROBBINS, MARY E · 2018 to 2022
$817k
NHLBI NIH HHS K08 HL124295NHLBI NIH HHS K08 HL140152
6 · The paper itself

Abstract

Thirty years ago, there was an emerging appreciation for the significance of oxidative stress in newborn disease. This prompted a renewed interest in the impact of oxygen therapy for the newborn in the delivery room and beyond, especially in premature infants. Today, the complexity of oxidative stress both in normal regulation and pathology is better understood, especially as it relates to neonatal mitochondrial oxidative stress responses to hyperoxia. Mitochondria are recipients of oxidative damage and have a propensity for oxidative self-injury that has been implicated in the pathogenesis of neonatal lung diseases. Similarly, both intrauterine growth restriction (IUGR) and macrosomia are associated with mitochondrial dysfunction and oxidative stress. Additionally, reoxygenation with 100% O

Indexed as

AntioxidantsBronchopulmonary DysplasiaFemaleFetal Growth RetardationFetusHumansHyperoxiaHypoxiaInfant, NewbornInfant, PrematureInflammationMitochondriaOxidative StressOxygenPregnancyReactive Oxygen SpeciesAntioxidantsOxygenReactive Oxygen SpeciesAntioxidant therapyBronchopulmonary dysplasia (BPD)Epigenetic changesGene-differentiationGrowthInflammation mitochondriaNewbornOxidative stressPersistent pulmonary hypertension of the newborn (PPHN)

Identifiers

PMID30954546
PMCPMC6791125
OpenAlexW2928134763

What OpenQuestion holds

Textmetadata
LicenceTDM
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.