Evidence map›Paper›PMID 32526683›Full record

ArticleNeuroImage. Clinical2020

Parental age effects on neonatal white matter development.

Oliver Gale-Grant, Daan Christiaens, Lucilio Cordero-Grande, Andrew Chew, Shona Falconer, Antonios Makropoulos, Nicholas Harper, Anthony N Price, Jana Hutter, Emer Hughes and 7 more

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Effect of advanced parental age on pregnancy outcome and offspring health.Journal of assisted reproduction and genetics · 2022
    Review
  5. Article
  6. Article
  7. Review
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

17 authors at 2 institutions in 1 country.

Oliver Gale-GrantCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom; MRC Centre for Neurodevelopmental Disorders, King's College London, United Kingdom; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom. Electronic address: oliver.gale-grant@kcl.ac.uk.
Daan ChristiaensCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Lucilio Cordero-GrandeCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Andrew ChewCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Shona FalconerCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Antonios MakropoulosDepartment of Computing, Imperial College London, United Kingdom.
Nicholas HarperCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Anthony N PriceCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Jana HutterCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Emer HughesCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Suresh VictorCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Serena J CounsellCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
Daniel RueckertDepartment of Computing, Imperial College London, United Kingdom.
Joseph V HajnalCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom.
A David EdwardsCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom; MRC Centre for Neurodevelopmental Disorders, King's College London, United Kingdom.
Jonathan O'MuircheartaighCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom; MRC Centre for Neurodevelopmental Disorders, King's College London, United Kingdom; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom.
Dafnis BatalleCentre for the Developing Brain, School of Imaging Sciences & Biomedical Engineering, King's College London, United Kingdom; Department of Forensic and Neurodevelopmental Science, Institute of Psychiatry, Psychology & Neuroscience, King's College London, United Kingdom.
King's College London · GBImperial College London · GB

Funding

Department of HealthEuropean Research Council 319456Medical Research Council MR/K006355/1Medical Research Council MR/N026063/1Medical Research Council MR/P502108/1Wellcome Trust 203148/Z/16/ZWellcome Trust 206675/Z/17/ZWellcome Trust 217316/Z/19/Z
6 · The paper itself

Abstract

objectiveAdvanced paternal age is associated with poor offspring developmental outcome. Though an increase in paternal age-related germline mutations may affect offspring white matter development, outcome differences could also be due to psychosocial factors. Here we investigate possible cerebral changes prior to strong environmental influences using brain MRI in a cohort of healthy term-born neonates.

methodsWe used structural and diffusion MRI images acquired soon after birth from a cohort (n = 275) of healthy term-born neonates. Images were analysed using a customised tract based spatial statistics (TBSS) processing pipeline. Neurodevelopmental assessment using the Bayley-III scales was offered to all participants at age 18 months. For statistical analysis neonates were compared in two groups, representing the upper quartile (paternal age ≥38 years) and lower three quartiles. The same method was used to assess associations with maternal age.

resultsIn infants with older fathers (≥38 years), fractional anisotropy, a marker of white matter organisation, was significantly reduced in three early maturing anatomical locations (the corticospinal tract, the corpus callosum, and the optic radiation). Fractional anisotropy in these locations correlated positively with Bayley-III cognitive composite score at 18 months in the advanced paternal age group. A small but significant reduction in total brain volume was also observed in in the infants of older fathers. No significant associations were found between advanced maternal age and neonatal imaging.

conclusionsThe epidemiological association between advanced paternal age and offspring outcome is extremely robust. We have for the first time demonstrated a neuroimaging phenotype of advanced paternal age before sustained parental interaction that correlates with later outcome.

Indexed as

BrainChild DevelopmentDiffusion Magnetic Resonance ImagingDiffusion Tensor ImagingFemaleGestational AgeHumansInfantInfant, NewbornInfant, PrematureMaleParentsPyramidal TractsWhite MatterBayleyBrain developmentDiffusion MRINewbornPaternal ageWhite matter

Identifiers

PMID32526683
PMCPMC7284122
OpenAlexW3028690587

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.