Evidence map›Paper›PMID 31362742›Full record

ArticleBMC pulmonary medicine2019

Caffeine is associated with improved alveolarization and angiogenesis in male mice following hyperoxia induced lung injury.

Vikramaditya Dumpa, Lori Nielsen, Huamei Wang, Vasantha H S Kumar

Open access · goldAbstract read
In one paragraph

Article in BMC pulmonary medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 12% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. Article
  6. Review
  7. [Expression and regulatory mechanism of miR-34a in neonatal rat model of bron-chopulmonary dysplasia induced by hyperoxia].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2025
    Article
  8. Review
  9. Article
  10. Review
  11. Updated perspective of EPAS1 and the role in pulmonary hypertension.Frontiers in cell and developmental biology · 2023
    Review
  12. Article
  13. Apnea of prematurity and sudden infant death syndrome.Handbook of clinical neurology · 2022
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. 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

4 authors at 2 institutions in 1 country.

Vikramaditya DumpaWinthrop University Hospital, Mineola, NY, USA.
Lori NielsenDivision of Neonatology, Department of Pediatrics, John R Oishei Children's Hospital, University at Buffalo, 1001 5th Floor Main Street, Buffalo, NY, 14203, USA.
Huamei WangDivision of Neonatology, Department of Pediatrics, John R Oishei Children's Hospital, University at Buffalo, 1001 5th Floor Main Street, Buffalo, NY, 14203, USA.
Vasantha H S KumarDivision of Neonatology, Department of Pediatrics, John R Oishei Children's Hospital, University at Buffalo, 1001 5th Floor Main Street, Buffalo, NY, 14203, USA. vkumar3@buffalo.edu.ORCID http://orcid.org/0000-0003-0950-2608
Women & Children's Hospital of Buffalo · USWinthrop-University Hospital · US

Funding

Marshall Klaus Grant NA
6 · The paper itself

Abstract

backgroundCaffeine therapy for apnea of prematurity reduces the incidence of bronchopulmonary dysplasia (BPD) in premature neonates. Several mechanisms, including improvement in pulmonary mechanics underly beneficial effects of caffeine in BPD. As vascular development promotes alveologenesis, we hypothesized that caffeine might enhance angiogenesis in the lung, promoting lung growth, thereby attenuating BPD.

methodsC57Bl/6 mice litters were randomized within 12 h of birth to room air (RA) or 95%O

resultsCaffeine and hyperoxia in itself upregulate HIF-2α and vascular endothelial growth factor gene expression. Protein expression of HIF-2α and VEGFR1 were higher in hyperoxia/caffeine and angiopoietin-1 lower in hyperoxia. An increase in radial alveolar count, secondary septal count, and septal length with a decrease in mean linear intercept indicate an amelioration of hyperoxic lung injury by caffeine. An increase in vessel surface area and a significant reduction in smooth muscle thickness of the pulmonary arterioles may suggest a beneficial effect of caffeine on vascular remodeling in hyperoxia, especially in male mice.

conclusionsPostnatal caffeine by modulating angiogenic gene expression early in lung development may restore the pulmonary microvasculature and alveolarization in adult lung.

Indexed as

Neovascularization, PhysiologicAngiopoietin-1AnimalsAnimals, NewbornBasic Helix-Loop-Helix ProteinsBronchopulmonary DysplasiaCaffeineDisease Models, AnimalEndothelial PAS Domain-Containing Protein 1HyperoxiaLungLung InjuryMaleMiceMice, Inbred C57BLPulmonary AlveoliAngiopoietin-1Basic Helix-Loop-Helix ProteinsCaffeineEndothelial PAS Domain-Containing Protein 1Flt1 protein, mouseVascular Endothelial Growth Factor Receptor-1CaffeineHyperoxiaHypoxia-inducible factorsLungMiceNewbornVEGF

Identifiers

PMID31362742
PMCPMC6668145
OpenAlexW2966768581

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.