Evidence map›Paper›PMID 39910445›Full record

ArticleJournal of neurodevelopmental disorders2025

Regional hippocampal thinning and gyrification abnormalities and associated cognition in children with prenatal alcohol exposure.

Blake A Gimbel, Jeffrey R Wozniak, Bryon A Mueller, Kent A Tuominen, Abigail M Ernst, Mary E Anthony, Erik de Water, CIFASD, Donovan J Roediger

Abstract read
In one paragraph

Article in Journal of neurodevelopmental disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Blake A GimbelNationwide Children's Hospital, Columbus, USA.
Jeffrey R WozniakUniversity of Minnesota Twin Cities, Minneapolis, USA. jwozniak@umn.edu.
Bryon A MuellerUniversity of Minnesota Twin Cities, Minneapolis, USA.
Kent A TuominenUniversity of Minnesota Twin Cities, Minneapolis, USA.
Abigail M ErnstUniversity of Minnesota Twin Cities, Minneapolis, USA.
Mary E AnthonyUniversity of Minnesota Twin Cities, Minneapolis, USA.
Erik de WaterGreat Lakes Neurobehavioral Center, Edina, USA.
CIFASD
Donovan J RoedigerUniversity of Minnesota Twin Cities, Minneapolis, USA.

Funding

Cross-Cultural Assessment of FASDU24AA014811 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI EDWARD P RILEY · 2003 to 2026
$13.1M
FASD in San Diego and Moscow (U01 Research Project)U01AA014834 · NIAAA · SAN DIEGO STATE UNIVERSITY · PI SARAH N MATTSON WELLER · 2003 to 2026
$12.4M
TRD4 - Ultrahigh Field Engineering and SafetyP41EB027061 · NIBIB · UNIVERSITY OF MINNESOTA · PI Gregory John Metzger · 2019 to 2026
$11.7M
NMR Imaging and SpectroscopyP41EB015894 · NIBIB · UNIVERSITY OF MINNESOTA · PI UGURBIL, KAMIL · 2012 to 2017
$8.4M
FASD Diagnostic Telemedicine ResourceU24AA014815 · NIAAA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Lauren Gist, SARAH N MATTSON WELLER · 2003 to 2026
$5.6M
Institutional Center Cores for Advanced NeuroimagingP30NS076408 · NINDS · UNIVERSITY OF MINNESOTA · PI UGURBIL, KAMIL · 2012 to 2020
$4.2M
tDCS and cognitive training as a neurodevelopmental intervention in FASDU01AA030164 · NIAAA · UNIVERSITY OF MINNESOTA · PI Jeffrey Robert Wozniak · 2022 to 2026
$2.2M
Multi-modal connectivity methods for the validation of Fetal Alcohol Spectrum Disorder diagnostic criteriaU01AA026102 · NIAAA · UNIVERSITY OF MINNESOTA · PI WOZNIAK, JEFFREY ROBERT · 2017 to 2021
$1.7M
High Performance Connectome Upgrade for Human 3T MR ScannerS10OD017974 · OD · UNIVERSITY OF MINNESOTA · PI LIM, KELVIN O. · 2014 to 2014
$600k
NIAAA NIH HHS 5U01AA014834NIAAA NIH HHS 5U01AA030164NIAAA NIH HHS U01 AA014834NIAAA NIH HHS U01 AA026102NIAAA NIH HHS U01 AA030164NIAAA NIH HHS U24 AA014811NIAAA NIH HHS U24 AA014815NIBIB NIH HHS P41 EB015894NIBIB NIH HHS P41 EB027061NIH HHS S10 OD017974NINDS NIH HHS P30 NS076408
6 · The paper itself

Abstract

backgroundPrenatal alcohol exposure (PAE) impacts hippocampal structure and function, contributing to deficits in memory and decision-making in affected individuals. Here, we evaluate hippocampal anomalies in children with PAE and an unexposed comparison group using advanced MRI methods that characterize hippocampal curvature and thickness.

methodsParticipants, ages 8 to 16 years, included children with PAE (n = 48) and an unexposed comparison group (n = 46) who underwent a dysmorphology exam, neuropsychological assessment, and an MRI scan. Height, weight, head circumference, and dysmorphic facial features were evaluated. Of those with PAE, 4.2% had fetal alcohol syndrome (FAS), 22.9% had partial FAS, and 72.9% had alcohol-related neurodevelopmental disorder. Neuropsychological testing included measures of intelligence and memory functioning. T1-weighted anatomical data were processed with the Hippunfold pipeline, which "unfolds" the complex hippocampal structure onto a template surface and provides measures of thickness and gyrification/curvature at each vertex. Permutation Analysis of Linear Models (PALM) was used to test for group differences (PAE vs. comparison) in hippocampal thickness and gyrification at each vertex and also to assess correlations with cognitive functioning.

resultsThere were significant regional differences in thickness and gyrification across bilateral hippocampi, with the PAE group showing substantially thinner tissue and less curvature than the comparison group, especially in CA1 and subiculum regions. For those with PAE, thinner subicular tissue (bilateral) was associated with lower IQ. Also in the PAE group, lower episodic memory performance was associated with thinness in the right hippocampus, especially in the subiculum region. There were no significant regional hippocampal patterns that were associated with cognitive functioning for individuals in the unexposed comparison group.

conclusionsWe used a novel MRI method to evaluate hippocampal structure in children with PAE and an unexposed comparison group. The data suggest that PAE disrupts hippocampal development, impacting both the early-stage folding of the structure and its ultimate thickness. The data also demonstrate that these developmental anomalies have functional consequences in terms of core memory functions as well as global intellectual functioning in children with PAE.

Indexed as

Fetal Alcohol Spectrum DisordersHippocampusPrenatal Exposure Delayed EffectsAdolescentChildCognitionFemaleHumansMagnetic Resonance ImagingMaleNeuropsychological TestsPregnancyCognitionFetal alcohol spectrum disordersHippocampal gyrificationHippocampal thicknessMemoryPrenatal alcohol exposure

Identifiers

PMID39910445
PMCPMC11796126

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.