Evidence map›Paper›PMID 27574995›Full record

ArticleThe Journal of pediatrics2016

Brain Dysplasia Associated with Ciliary Dysfunction in Infants with Congenital Heart Disease.

Ashok Panigrahy, Vincent Lee, Rafael Ceschin, Giulio Zuccoli, Nancy Beluk, Omar Khalifa, Jodie K Votava-Smith, Mark DeBrunner, Ricardo Munoz, Yuliya Domnina and 6 more

Abstract read
In one paragraph

Article in The Journal of pediatrics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Motile ciliopathies.Nature reviews. Disease primers · 2020
    Review
  14. Article
  15. Review
  16. The answer is cilia, whatever the question may be!Annals of translational medicine · 2018
    Article
  17. Article
  18. Article
  19. Chronic Blockade of Brain Endothelin Receptor Type-A (ETInternational journal of molecular sciences · 2018
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Ashok PanigrahyDepartment of Pediatric Radiology, Childrens Hospital of Pittsburgh of University of Pittsburgh Medical Center and University of Pittsburgh School of Medicine, Pittsburgh, PA; Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA. Electronic address: panigrahya@upmc.edu.
Vincent LeeDepartment of Pediatric Radiology, Childrens Hospital of Pittsburgh of University of Pittsburgh Medical Center and University of Pittsburgh School of Medicine, Pittsburgh, PA.
Rafael CeschinDepartment of Pediatric Radiology, Childrens Hospital of Pittsburgh of University of Pittsburgh Medical Center and University of Pittsburgh School of Medicine, Pittsburgh, PA; Department of Biomedical Informatics, University of Pittsburgh, Pittsburgh, PA.
Giulio ZuccoliDepartment of Pediatric Radiology, Childrens Hospital of Pittsburgh of University of Pittsburgh Medical Center and University of Pittsburgh School of Medicine, Pittsburgh, PA.
Nancy BelukDepartment of Pediatric Radiology, Childrens Hospital of Pittsburgh of University of Pittsburgh Medical Center and University of Pittsburgh School of Medicine, Pittsburgh, PA.
Omar KhalifaDepartment of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Jodie K Votava-SmithDepartment of Pediatrics, Division of Cardiology, Childrens Hospital of Los Angeles, Los Angeles, CA.
Mark DeBrunnerDivision of Pediatric Cardiology, Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Ricardo MunozCardiac Intensive Care Division, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Yuliya DomninaCardiac Intensive Care Division, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Victor MorellDivision of Pediatric Cardiothoracic Surgery, Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Peter WeardenDivision of Pediatric Cardiothoracic Surgery, Department of Surgery, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Joan Sanchez De ToledoCardiac Intensive Care Division, University of Pittsburgh School of Medicine, Pittsburgh, PA.
William DevineDepartment of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Maliha ZahidDepartment of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Cecilia W LoDepartment of Developmental Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA.

Funding

The internship in Biomedical Research, Informatics, and Computer Science (iBRIC): Biomedical Informatics and Data Science research experiences for students from Minority Serving InstitutionsT15LM007059 · NLM · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HARRY S HOCHHEISER · 1987 to 2026
$23.9M
Advanced MR Imaging of Perinatal White Matter InjuryK23NS063371 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI PANIGRAHY, ASHOK · 2009 to 2013
$846k
NINDS NIH HHS K23 NS063371NLM NIH HHS T15 LM007059
6 · The paper itself

Abstract

objectiveTo test for associations between abnormal respiratory ciliary motion (CM) and brain abnormalities in infants with congenital heart disease (CHD) STUDY

designWe recruited 35 infants with CHD preoperatively and performed nasal tissue biopsy to assess respiratory CM by videomicroscopy. Cranial ultrasound scan and brain magnetic resonance imaging were obtained pre- and/or postoperatively and systematically reviewed for brain abnormalities. Segmentation was used to quantitate cerebrospinal fluid and regional brain volumes. Perinatal and perioperative clinical variables were collected.

resultsA total of 10 (28.5%) patients with CHD had abnormal CM. Abnormal CM was not associated with brain injury but was correlated with increased extraaxial cerebrospinal fluid volume (P < .001), delayed brain maturation (P < .05), and a spectrum of subtle dysplasia including the hippocampus (P < .0078) and olfactory bulb (P < .034). Abnormal CM was associated with higher composite dysplasia score (P < .001), and both were correlated with elevated preoperative serum lactate (P < .001).

conclusionsAbnormal respiratory CM in infants with CHD is associated with a spectrum of brain dysplasia. These findings suggest that ciliary defects may play a role in brain dysplasia in patients with CHD and have the potential to prognosticate neurodevelopmental risks.

Indexed as

BrainBrain DiseasesCiliary Motility DisordersFemaleHeart Defects, CongenitalHumansInfantInfant, NewbornMagnetic Resonance ImagingMaleProspective Studieschoroid plexusextraaxial CSFhippocampusmotile ciliaolfactory

Identifiers

PMID27574995
PMCPMC5085835

What OpenQuestion holds

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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.