Evidence map›Paper›PMID 42563976›Full record

ArticleAnnals of the Child Neurology Society2025

Variation in Neurodegeneration-Linked Brain Regions in Young Adult APOE E4 Carriers With Spina Bifida.

Joan M Jasien, Jacques A Stout, Mohamad A Mikati, Robert J Anderson, Brittany G Nave, Herbert E Fuchs, Brian Smith, Alexandra Badea, Jeffrey N Browndyke

Abstract read
In one paragraph

Article in Annals of the Child Neurology Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Joan M JasienDivision of Pediatric Neurology and Developmental Medicine, Department of Pediatrics Duke University Medical Center Durham North Carolina USA.ORCID https://orcid.org/0000-0002-5469-1092
Jacques A StoutBrain Imaging & Analysis Center Duke University Durham North Carolina USA.
Mohamad A MikatiDivision of Pediatric Neurology and Developmental Medicine, Department of Pediatrics Duke University Medical Center Durham North Carolina USA.
Robert J AndersonQuantitative Imaging and Analysis Laboratory, Department of Radiology Duke University School of Medicine Durham North Carolina USA.
Brittany G NaveDivision of Pediatric Neurology and Developmental Medicine, Department of Pediatrics Duke University Medical Center Durham North Carolina USA.
Herbert E FuchsDepartment of Neurosurgery Duke University School of Medicine Durham North Carolina USA.
Brian SmithDivision of Neonatology, Department of Pediatrics Duke University Medical Center Durham North Carolina USA.
Alexandra BadeaBrain Imaging & Analysis Center Duke University Durham North Carolina USA.
Jeffrey N BrowndykeBrain Imaging & Analysis Center Duke University Durham North Carolina USA.

Funding

Sex and APOE genotype interact to alter immune regulated metabolism in ADRF1AG057895 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA, COLTON, CAROL ANNE · 2019 to 2019
$5.8M
Brain networks in mouse models of agingR01AG066184 · NIA · DUKE UNIVERSITY · PI BADEA, ALEXANDRA · 2019 to 2023
$3.8M
Cardiac photon counting CT and its application in studying interactions between Alzheimer's and heart diseaseRF1AG070149 · NIA · DUKE UNIVERSITY · PI BADEA, CRISTIAN T · 2021 to 2022
$2.1M
NIA NIH HHS R01 AG066184NIA NIH HHS RF1 AG057895NIA NIH HHS RF1 AG070149
6 · The paper itself

Abstract

Objective: Possible pleiotropic effects of apolipoprotein E4 (APOE E4) in individuals with congenital brain malformations are relatively unknown. Our goal was to determine if neurodegeneration-linked brain region volumes differ significantly between E4 carriers and noncarriers in young adults with spina bifida (SB). Methods: Eleven individuals ( > 18 years), genotyped for APOE, underwent neuroimaging and neurocognitive evaluation. Primary analysis: Magnetic resonance imaging (MRI) data from 10 a priori neurodegeneration-risk regions of interest were compared between E4 carriers and noncarriers, adjusting for age, sex, and total intracranial volume (FDR-adjusted Results: Comparison of a priori risk region volumes revealed significantly lower left amygdala volumes (FDR-adjusted Interpretation: Early left amygdala volumetric reduction was found in E4 carriers; combined group volume comparisons revealed frontal and temporal lobe differences in young adults with SB relative to age- and sex-matched volumetric estimates. This pilot investigation does not appear to support E4 conferring a pleiotropic benefit in young adults with SB but rather supports further investigation of MRI volumetrics as a possible biomarker for this population.

Indexed as

amygdalaAPOEMRINeuroQuantspina bifida

Identifiers

PMID42563976
PMCPMC13359342

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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.