Evidence map›Paper›PMID 36136598›Full record

ArticleThe Journal of clinical investigation2022

Neonatal hyperoxia in mice triggers long-term cognitive deficits via impairments in cerebrovascular function and neurogenesis.

Marissa A Lithopoulos, Xavier Toussay, Shumei Zhong, Liqun Xu, Shamimunisa B Mustafa, Julie Ouellette, Moises Freitas-Andrade, Cesar H Comin, Hayam A Bassam, Adam N Baker and 12 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
4.7field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 32 citations in OpenAlex.

  1. Titrating cumulative neonatal hyperoxia in mice to model bronchopulmonary dysplasia severities.American journal of respiratory cell and molecular biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Targeting adenosine APurinergic signalling · 2025
    Review
  13. Article
  14. βMedicinal research reviews · 2025
    Review
  15. Article
  16. Article
  17. The role of NLRP3 inflammasome-mediated pyroptosis in astrocytes during hyperoxia-induced brain injury.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  18. Review
  19. Article
  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

22 authors at 5 institutions in 3 countries.

Marissa A LithopoulosRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Xavier ToussayNeuroscience Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Shumei ZhongRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Liqun XuRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Shamimunisa B MustafaUniversity of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Julie OuelletteDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Moises Freitas-AndradeNeuroscience Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Cesar H CominDepartment of Computer Science, Federal University of São Carlos, São Carlos, Brazil.
Hayam A BassamNeuroscience Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Adam N BakerNeuroscience Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Yiren SunRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Michael WakemThermo Fisher Scientific, Burlington, Ontario, Canada.
Alvaro G MoreiraUniversity of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Cynthia L BlancoUniversity of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Arul VadivelRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Catherine TsilfidisDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Steven R SeidnerUniversity of Texas Health Science Center at San Antonio, San Antonio, Texas, USA.
Ruth S SlackDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Diane C LagaceDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Jing WangRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
Baptiste LacosteDepartment of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, Ontario, Canada.
Bernard ThébaudRegenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.
University of Ottawa · CAOttawa Hospital · CAThe University of Texas Health Science Center at San Antonio · USThermo Fisher Scientific (Canada) · CAUniversidade Federal de São Carlos · BR

Funding

CIHR
6 · The paper itself

Abstract

Preterm birth is the leading cause of death in children under 5 years of age. Premature infants who receive life-saving oxygen therapy often develop bronchopulmonary dysplasia (BPD), a chronic lung disease. Infants with BPD are at a high risk of abnormal neurodevelopment, including motor and cognitive difficulties. While neural progenitor cells (NPCs) are crucial for proper brain development, it is unclear whether they play a role in BPD-associated neurodevelopmental deficits. Here, we show that hyperoxia-induced experimental BPD in newborn mice led to lifelong impairments in cerebrovascular structure and function as well as impairments in NPC self-renewal and neurogenesis. A neurosphere assay utilizing nonhuman primate preterm baboon NPCs confirmed impairment in NPC function. Moreover, gene expression profiling revealed that genes involved in cell proliferation, angiogenesis, vascular autoregulation, neuronal formation, and neurotransmission were dysregulated following neonatal hyperoxia. These impairments were associated with motor and cognitive decline in aging hyperoxia-exposed mice, reminiscent of deficits observed in patients with BPD. Together, our findings establish a relationship between BPD and abnormal neurodevelopmental outcomes and identify molecular and cellular players of neonatal brain injury that persist throughout adulthood that may be targeted for early intervention to aid this vulnerable patient population.

Indexed as

Bronchopulmonary DysplasiaCognitive DysfunctionHyperoxiaPremature BirthAnimalsAnimals, NewbornCognitionFemaleHumansInfant, NewbornLungMiceNeurogenesisBehaviorNeurodevelopmentNeuronal stem cellsNeuroscienceStem cells

Identifiers

PMID36136598
PMCPMC9663164
OpenAlexW4296685469

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.