Evidence map›Paper›PMID 20087186›Full record

ReviewCurrent opinion in pediatrics2010

Genetics of bronchopulmonary dysplasia in the age of genomics.

Pascal M Lavoie, Marie-Pierre Dubé

Abstract readReview
In one paragraph

Review in Current opinion in pediatrics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Trial
  2. Article
  3. Review
  4. Review
  5. Hydrogen sulfide, oxygen, and calcium regulation in developing human airway smooth muscle.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  6. Physiological reports · 2017
    Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Animal models of bronchopulmonary dysplasia. The term mouse models.American journal of physiology. Lung cellular and molecular physiology · 2014
    Review
  13. Article
  14. Epidemiology of bronchopulmonary dysplasia.Birth defects research. Part A, Clinical and molecular teratology · 2014
    Review
  15. A 24-year-old woman with episodes of shortness of breath, cough and wheezing.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2013
    Article
  16. Toll-like receptor genetic variants are associated with Gram-negative infections in VLBW infants.Journal of perinatology : official journal of the California Perinatal Association · 2013
    Article
  17. Article
  18. Article
  19. Histological chorioamnionitis and bronchopulmonary dysplasia: a retrospective cohort study.Journal of perinatology : official journal of the California Perinatal Association · 2013
    Article
  20. Chorioamnionitis and lung injury in preterm newborns.Critical care research and practice · 2013
    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

2 authors.

Pascal M LavoieChild & Family Research Institute, University of British Columbia, Vancouver, Canada. plavoie@cw.bc.ca
Marie-Pierre Dubé

Funding

CIHR 94325-1
6 · The paper itself

Abstract

purpose of reviewAccording to recent evidence, susceptibility to bronchopulmonary dysplasia (BPD) in preterm infants is predominantly inherited. The purpose of this review is to discuss current published genetic association studies in light of the accumulated knowledge in genomics. RECENT

findingsMajor advances in the development of next-generation genotyping and sequencing platforms, statistical methodologies, inventories of functional outcome of some common genetic polymorphisms and large-scale cataloguing of genetic variability among many of the world's ethnic populations have greatly facilitated the study of polygenic conditions. For BPD, genetic-association studies have primarily focused on components of innate (e.g. first-line) immune and antioxidant defences, mechanisms of vascular and lung remodelling, and surfactant proteins. However, studies have been limited in sample size and therefore fraught with a high probability of false-positive and false-negative associations. Nonetheless, candidate gene associations have indicated some novel biological pathways and provide a conceptual framework for the design of larger, collaborative population-based studies. SUMMARY: Although studies to date have not been able to identify reproducible genetic risk markers for BPD, they have directed us towards new, promising research avenues.

Indexed as

Bronchopulmonary DysplasiaGenomicsHumansInfant, Newborn

Identifiers

PMID20087186
PMCPMC5104534

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.