Evidence map›Paper›PMID 25379416›Full record

Trial reportNeuroImage. Clinical2014

Neural compensation in adulthood following very preterm birth demonstrated during a visual paired associates learning task.

Philip J Brittain, Sean Froudist Walsh, Kie-Woo Nam, Vincent Giampietro, Vyacheslav Karolis, Robin M Murray, Sagnik Bhattacharyya, Anastasia Kalpakidou, Chiara Nosarti

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in NeuroImage. Clinical, 2014. 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
2.5field-weighted citation impact, top 10% 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, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Advances in functional and diffusion neuroimaging research into the long-term consequences of very preterm birth.Journal of perinatology : official journal of the California Perinatal Association · 2021
    Review
  5. Breakdown of Whole-brain Dynamics in Preterm-born Children.Cerebral cortex (New York, N.Y. : 1991) · 2020
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  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

9 authors at 1 institution in 1 country.

Philip J BrittainDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
Sean Froudist WalshDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
Kie-Woo NamDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
Vincent GiampietroDepartment of Neuroimaging, Centre for Neuroimaging Sciences, Institute of Psychiatry, King's College London, De Crespigny Park, London SE5 8AF, UK.
Vyacheslav KarolisDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
Robin M MurrayDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
Sagnik BhattacharyyaDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
Anastasia KalpakidouDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
Chiara NosartiDepartment of Psychosis Studies, Neurodevelopment and Mental Health Group, Institute of Psychiatry, King's College London, De Crespigny Park, London, SE5 8AF, UK.
King's College London · GB

Funding

Department of Health NIHR-CS-011-001Medical Research Council G0501775
6 · The paper itself

Abstract

Very preterm birth (VPT; < 33 weeks of gestation) is associated with an increased risk of learning disability, which contributes to more VPT-born children repeating grades and underachieving in school. Learning problems associated with VPT birth may be caused by pathophysiological alterations in neurodevelopment resulting from perinatal brain insult; however, adaptive neuroplastic processes may subsequently occur in the developing preterm brain which ameliorate, to an extent, the potential sequelae of altered neurophysiology. Here, we used functional magnetic resonance imaging (fMRI) to compare neuronal activation in 24 VPT individuals and 22 controls (CT) in young adulthood during a learning task consisting of the encoding and subsequent recognition of repeated visual paired associates. Structural MRI data were also collected and analysed in order to explore possible structure-function associations. Whilst the two groups did not differ in their learning ability, as demonstrated by their capacity to recognize previously-seen and previously-unseen visual pairs, between-group differences in linear patterns of Blood Oxygenation Level Dependant (BOLD) activity were observed across the four repeated blocks of the task for both the encoding and recognition conditions, suggesting that the way learning takes place differs between the two groups. During encoding, significant between-group differences in patterns of BOLD activity were seen in clusters centred on the cerebellum, the anterior cingulate gyrus, the midbrain/substantia nigra, medial temporal (including parahippocampal) gyrus and inferior and superior frontal gyri. During the recognition condition, significant between-group differences in patterns of BOLD activity were seen in clusters centred on the claustrum and the posterior cerebellum. Structural analysis revealed smaller grey matter volume in right middle temporal gyrus in VPT individuals compared to controls, however volume in this region was not significantly associated with functional activation. These results demonstrate that although cognitive task performance between VPT individuals and controls may be comparable on certain measures, differences in BOLD signal may also be evident, some of which could represent compensatory neural processes following VPT-related brain insult.

Indexed as

Adaptation, PhysiologicalAssociation LearningBrainFemaleFollow-Up StudiesHumansInfant, NewbornInfant, Very Low Birth WeightMagnetic Resonance ImagingMalePhotic StimulationPremature BirthYoung AdultfMRILearning disabilityNeuroplasticityVery preterm birthVisual paired associates

Identifiers

PMID25379416
PMCPMC4215530
OpenAlexW2064396942

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.