Evidence map›Paper›PMID 28302742›Full record

ReviewCirculation research2017

Neurodevelopmental Abnormalities and Congenital Heart Disease: Insights Into Altered Brain Maturation.

Paul D Morton, Nobuyuki Ishibashi, Richard A Jonas

Open access · bronzeAbstract readReview
In one paragraph

Review in Circulation research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 1 pooled it
9.3field-weighted citation impact, top 1% 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

96 citing papers in PubMed, 1 synthesis or guideline pooled it, 188 citations in OpenAlex.

  1. Pooled it
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  20. Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genes.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article

36 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Paul D MortonFrom the Center for Neuroscience Research and Children's National Heart Institute, Children's National Health System, Washington, DC.
Nobuyuki IshibashiFrom the Center for Neuroscience Research and Children's National Heart Institute, Children's National Health System, Washington, DC. rjonas@childrensnational.org nishibas@childrensnational.org.
Richard A JonasFrom the Center for Neuroscience Research and Children's National Heart Institute, Children's National Health System, Washington, DC. rjonas@childrensnational.org nishibas@childrensnational.org.
Children's National · US

Funding

Research_ProjectU54HD090257 · NICHD · CHILDREN'S RESEARCH INSTITUTE · PI VITTORIO GALLO, VITTORIO GALLO VITTORIO GALLO · 2016 to 2020
$5.9M
Aberrations in oligodendrocyte development resulting from congenital heart disease and its surgical treatmentR01HL128546 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI JONAS, RICHARD A · 2015 to 2018
$3.0M
Protection of Developing White Matter during Cardiac SurgeryR01HL104173 · NHLBI · CHILDREN'S RESEARCH INSTITUTE · PI JONAS, RICHARD A · 2010 to 2014
$2.4M
NHLBI NIH HHS R01 HL104173NHLBI NIH HHS R01 HL128546NICHD NIH HHS U54 HD090257
6 · The paper itself

Abstract

In the past 2 decades, it has become evident that individuals born with congenital heart disease (CHD) are at risk of developing life-long neurological deficits. Multifactorial risk factors contributing to neurodevelopmental abnormalities associated with CHD have been identified; however, the underlying causes remain largely unknown, and efforts to address this issue have only recently begun. There has been a dramatic shift in focus from newly acquired brain injuries associated with corrective and palliative heart surgery to antenatal and preoperative factors governing altered brain maturation in CHD. In this review, we describe key time windows of development during which the immature brain is vulnerable to injury. Special emphasis is placed on the dynamic nature of cellular events and how CHD may adversely impact the cellular units and networks necessary for proper cognitive and motor function. In addition, we describe current gaps in knowledge and offer perspectives about what can be done to improve our understanding of neurological deficits in CHD. Ultimately, a multidisciplinary approach will be essential to prevent or improve adverse neurodevelopmental outcomes in individuals surviving CHD.

Indexed as

AnimalsBrainCerebrovascular CirculationHeart Defects, CongenitalHumansNeurodevelopmental Disordersbrainmodels, animalneuroimagingrisk factors

Identifiers

PMID28302742
PMCPMC5409515
OpenAlexW2595829182

What OpenQuestion holds

Textmetadata
LicenceTDM
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.