Evidence map›Paper›PMID 24993047›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2014

Aminoglycoside-mediated relaxation of the ductus arteriosus in sepsis-associated PDA.

Megan M Vucovich, Robert B Cotton, Elaine L Shelton, Jeremy A Goettel, Noah J Ehinger, Stanley D Poole, Naoko Brown, James L Wynn, Bibhash C Paria, James C Slaughter and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. A novel role for PGEAmerican journal of physiology. Heart and circulatory physiology · 2023
    Article
  6. Article
  7. Article
  8. Review
  9. Mouse models of patent ductus arteriosus (PDA) and their relevance for human PDA.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Review
  10. Association of chorioamnionitis and patent ductus arteriosus in a national U.S. cohort.Journal of perinatology : official journal of the California Perinatal Association · 2021
    Article
  11. Article
  12. Article
  13. Genetic variants associated with patent ductus arteriosus in extremely preterm infants.Journal of perinatology : official journal of the California Perinatal Association · 2019
    Article
  14. Article
  15. IL-17 in neonatal health and disease.American journal of reproductive immunology (New York, N.Y. : 1989) · 2018
    Review
  16. Article
  17. Selective serotonin reuptake inhibitor exposure constricts the mouse ductus arteriosus in utero.American journal of physiology. Heart and circulatory physiology · 2016
    Article
  18. [Risk factors for patent ductus arteriosus in early preterm infants: a case-control study].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2016
    Article
  19. 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

13 authors at 3 institutions in 1 country.

Megan M VucovichDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
Robert B CottonDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
Elaine L SheltonDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
Jeremy A GoettelDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
Noah J EhingerDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
Stanley D PooleDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
Naoko BrownDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
James L WynnDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
Bibhash C PariaDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee;
James C SlaughterDepartment of Biostatistics, Vanderbilt University School of Medicine, Nashville, Tennessee;
Reese H ClarkPediatrix Medical Group, Sunrise, Florida; and.
Mario A RojasDepartment of Pediatrics, Wake Forest University School of Medicine, Winston Salem, North Carolina.
Jeff ReeseDepartment of Pediatrics, Vanderbilt University School of Medicine and the Monroe Carell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee; Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, Tennessee; jeff.reese@vanderbilt.edu.
Vanderbilt University · USMonroe Carell Jr. Children's Hospital · USWake Forest University · US

Funding

Genes contributing to patent ductus arteriosus susceptibility in preterm newbornsR01HL109199 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CLYMAN, RONALD I · 2011 to 2014
$3.0M
Hamster: A Unique Model for Studying ImplantationR01HD044741 · NICHD · VANDERBILT UNIVERSITY · PI PARIA, BIBHASH CHANDRA · 2004 to 2014
$2.9M
Mechanisms of Ductus Arteriosus RegulationR01HL077395 · NHLBI · VANDERBILT UNIVERSITY · PI REESE, JOHN JEFFREY · 2006 to 2010
$2.0M
Role of natriuretic peptides in the ductus arteriosusR01HL096967 · NHLBI · VANDERBILT UNIVERSITY · PI REESE, JOHN JEFFREY · 2010 to 2013
$1.5M
The Role of the Inflammasome in Neonatal SepsisK08GM106143 · NIGMS · VANDERBILT UNIVERSITY · PI WYNN, JAMES LAWRENCE · 2013 to 2017
$875k
NHLBI NIH HHS HL-109199NHLBI NIH HHS HL-77395NHLBI NIH HHS HL-96967NHLBI NIH HHS R01 HL077395NHLBI NIH HHS R01 HL096967NHLBI NIH HHS R01 HL109199NICHD NIH HHS HD-44741NICHD NIH HHS R01 HD044741NIGMS NIH HHS GM-106143NIGMS NIH HHS K08 GM106143
6 · The paper itself

Abstract

Sepsis is strongly associated with patency of the ductus arteriosus (PDA) in critically ill newborns. Inflammation and the aminoglycoside antibiotics used to treat neonatal sepsis cause smooth muscle relaxation, but their contribution to PDA is unknown. We examined whether: 1) lipopolysaccharide (LPS) or inflammatory cytokines cause relaxation of the ex vivo mouse DA; 2) the aminoglycosides gentamicin, tobramycin, or amikacin causes DA relaxation; and 3) newborn infants treated with aminoglycosides have an increased risk of symptomatic PDA (sPDA). Changes in fetal mouse DA tone were measured by pressure myography in response to LPS, TNF-α, IFN-γ, macrophage-inflammatory protein 2, IL-15, IL-13, CXC chemokine ligand 12, or three aminoglycosides. A clinical database of inborn patients of all gestations was analyzed for association between sPDA and aminoglycoside treatment. Contrary to expectation, neither LPS nor any of the inflammatory mediators caused DA relaxation. However, each of the aminoglycosides caused concentration-dependent vasodilation in term and preterm mouse DAs. Pretreatment with indomethacin and N-(G)-nitro-L-arginine methyl ester did not prevent gentamicin-induced DA relaxation. Gentamicin-exposed DAs developed less oxygen-induced constriction than unexposed DAs. Among 488,349 infants who met the study criteria, 40,472 (8.3%) had sPDA. Confounder-adjusted odds of sPDA were higher in gentamicin-exposed infants, <25 wk and >32 wk. Together, these findings suggest that factors other than inflammation contribute to PDA. Aminoglycoside-induced vasorelaxation and inhibition of oxygen-induced DA constriction support the paradox that antibiotic treatment of sepsis may contribute to DA relaxation. This association was also found in newborn infants, suggesting that antibiotic selection may be an important consideration in efforts to reduce sepsis-associated PDA.

Indexed as

VasodilationAnimalsChemokine CXCL12Ductus ArteriosusDuctus Arteriosus, PatentGentamicinsHumansIndomethacinInfant, NewbornInterferon-gammaInterleukinsIn Vitro TechniquesLipopolysaccharidesMiceMice, Inbred C57BLNG-Nitroarginine Methyl EsterChemokine CXCL12GentamicinsIndomethacinInterferon-gammaInterleukinsLipopolysaccharidesNG-Nitroarginine Methyl EsterTumor Necrosis Factor-alphaaminoglycosidecytokineductus arteriosusendotoxingentamicinhumanlipopolysaccharidemouse

Identifiers

PMID24993047
PMCPMC4187398
OpenAlexW2314064273

What OpenQuestion holds

Textmetadata
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.