Evidence map›Paper›PMID 32413023›Full record

ArticlePloS one2020

Pulmonary ductal coarctation and left pulmonary artery interruption; pathology and role of neural crest and second heart field during development.

Adriana C Gittenberger-de Groot, Joshua C Peterson, Lambertus J Wisse, Arno A W Roest, Robert E Poelmann, Regina Bökenkamp, Nynke J Elzenga, Mark Hazekamp, Margot M Bartelings, Monique R M Jongbloed and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Total Anomalous Pulmonary Venous Connections, Human Genetics.Advances in experimental medicine and biology · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. 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

11 authors at 2 institutions in 1 country.

Adriana C Gittenberger-de GrootDepartment of Cardiology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0001-6062-4112
Joshua C PetersonDepartment of Anatomy & Embryology, Leiden University Medical Center, Leiden, The Netherlands.
Lambertus J WisseDepartment of Anatomy & Embryology, Leiden University Medical Center, Leiden, The Netherlands.
Arno A W RoestDepartment of Anatomy & Embryology, Leiden University Medical Center, Leiden, The Netherlands.
Robert E PoelmannDepartment of Cardiology, Leiden University Medical Center, Leiden, The Netherlands.
Regina BökenkampDepartment of Pediatric Cardiology, Leiden University Medical Center, Leiden, The Netherlands.
Nynke J ElzengaDepartment of Anatomy & Embryology, Leiden University Medical Center, Leiden, The Netherlands.
Mark HazekampDepartment of Cardio-thoracic Surgery, Leiden University Medical Center, Leiden, The Netherlands.
Margot M BartelingsDepartment of Anatomy & Embryology, Leiden University Medical Center, Leiden, The Netherlands.
Monique R M JongbloedDepartment of Cardiology, Leiden University Medical Center, Leiden, The Netherlands.
Marco C DeRuiterDepartment of Anatomy & Embryology, Leiden University Medical Center, Leiden, The Netherlands.
Leiden University Medical Center · NLLeiden University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesIn congenital heart malformations with pulmonary stenosis to atresia an abnormal lateral ductus arteriosus to left pulmonary artery connection can lead to a localised narrowing (pulmonary ductal coarctation) or even interruption We investigated embryonic remodelling and pathogenesis of this area. MATERIAL AND

methodsNormal development was studied in WntCre reporter mice (E10.0-12.5) for neural crest cells and Nkx2.5 immunostaining for second heart field cells. Data were compared to stage matched human embryos and a VEGF120/120 mutant mouse strain developing pulmonary atresia.

resultsNormal mouse and human embryos showed that the mid-pharyngeal endothelial plexus, connected side-ways to the 6th pharyngeal arch artery. The ventral segment formed the proximal pulmonary artery. The dorsal segment (future DA) was solely surrounded by neural crest cells. The ventral segment had a dual outer lining with neural crest and second heart field cells, while the distal pulmonary artery was covered by none of these cells. The asymmetric contribution of second heart field to the future pulmonary trunk on the left side of the aortic sac (so-called pulmonary push) was evident. The ventral segment became incorporated into the pulmonary trunk leading to a separate connection of the left and right pulmonary arteries. The VEGF120/120 embryos showed a stunted pulmonary push and a variety of vascular anomalies. SUMMARY: Side-way connection of the DA to the left pulmonary artery is a congenital anomaly. The primary problem is a stunted development of the pulmonary push leading to pulmonary stenosis/atresia and a subsequent lack of proper incorporation of the ventral segment into the aortic sac. Clinically, the aberrant smooth muscle tissue of the ductus arteriosus should be addressed to prohibit development of severe pulmonary ductal coarctation or even interruption of the left pulmonary artery.

Indexed as

AnimalsAortaDuctus ArteriosusHomeobox Protein Nkx-2.5HumansMiceMice, Inbred C57BLNeural CrestPulmonary ArteryPulmonary AtresiaVascular Endothelial Growth Factor AHomeobox Protein Nkx-2.5Vascular Endothelial Growth Factor A

Identifiers

PMID32413023
PMCPMC7228067
OpenAlexW3025802736

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.