Evidence map›Paper›PMID 40488346›Full record

Observational studyAnnals of neurology2025

Punctate White Matter Abnormality in Moderate-to-Late Preterm Infants.

Eleanor Kennedy, Ting Guo, Sian Williams, Thiviya Selvanathan, Jane M Alsweiler, Frank H Bloomfield, Malcolm Battin, David Dubowitz, Steven P Miller, Catherine Morgan and 4 more

Abstract readObservational Study
In one paragraph

Observational study in Annals of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

14 authors.

Eleanor KennedyLiggins Institute, University of Auckland, Auckland, New Zealand.ORCID 0000-0002-7000-0087
Ting GuoNeurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Canada.ORCID 0000-0001-5866-4262
Sian WilliamsLiggins Institute, University of Auckland, Auckland, New Zealand.
Thiviya SelvanathanNeurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Canada.
Jane M AlsweilerAuckland District Health Board, Auckland, New Zealand.
Frank H BloomfieldLiggins Institute, University of Auckland, Auckland, New Zealand.
Malcolm BattinNewborn Services, Health New Zealand, Te Toka Tumai Auckland, Auckland, New Zealand.
David DubowitzCentre for Advanced MRI, University of Auckland, Auckland, New Zealand.
Steven P MillerNeurosciences and Mental Health, The Hospital for Sick Children Research Institute, Toronto, Canada.
Catherine MorganCentre for Advanced MRI, University of Auckland, Auckland, New Zealand.
David PerryStarship Children's Health, Te Toka Tumai Auckland, Auckland, New Zealand.
Ngaire Susan StottAuckland District Health Board, Auckland, New Zealand.
Jane E HardingLiggins Institute, University of Auckland, Auckland, New Zealand.
MR DIAMOND and MoPED Study Groups

Funding

Cerebral Palsy Alliance Research Foundation 02821Health Research Council of New Zealand 16/605Health Research Council of New Zealand 18/407Health Research Council of New Zealand 22/113The Jubilee Crippled Children Foundation Trust
6 · The paper itself

Abstract

objectiveModerate-to-late preterm (MLP) infants contribute to the greatest proportion of preterm children with neurodevelopmental impairments. White matter injury (WMI) is common and predicts adverse outcomes in very preterm (VP) infants. However, little is known about white matter abnormality (WMA) in MLP infants. We investigated the burden and distribution of WMA in MLP infants.

methodsMLP infants were recruited from a randomized trial on neonatal nutrition and a prospective observational cohort in New Zealand, and underwent brain magnetic resonance imaging (MRI) soon after birth and at term-equivalent age (TEA). WMA was manually segmented using an established method. Total and regional WMA volumes and percentage of WMA to total cerebral volume were calculated. Probabilistic WMA maps were generated and compared with WMI in VP infants and term infants with congenital heart disease.

resultsOf 101 infants (32 females), 40 (39.6%) had WMA on at least 1 scan. In 37 infants with WMA who had both scans, WMA was less visible in 22 (59.5%) or undetectable in 7 (18.9%) infants with a mean reduction of 72.7 ± 207.5 mm

interpretationWMA is much more common in MLP infants than previously reported and occurs in a characteristic topology. WMA may be missed on TEA MRI, and its relationship with outcomes in MLP infants warrants attention. ANN NEUROL 2025;98:329-340.

Indexed as

BrainInfant, PrematureWhite MatterFemaleHumansInfantInfant, NewbornMagnetic Resonance ImagingMaleNew ZealandProspective Studies

Identifiers

PMID40488346
PMCPMC12278191

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.