Evidence map›Paper›PMID 28247416›Full record

ArticleAlcoholism, clinical and experimental research2017

Heavy Prenatal Alcohol Exposure is Related to Smaller Corpus Callosum in Newborn MRI Scans.

Sandra W Jacobson, Joseph L Jacobson, Christopher D Molteno, Christopher M R Warton, Pia Wintermark, H Eugene Hoyme, Greetje De Jong, Paul Taylor, Fleur Warton, Nadine M Lindinger and 7 more

Abstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 2 pooled it
10.2field-weighted citation impact, top 2% 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

47 citing papers in PubMed, 2 syntheses or guidelines pooled it, 71 citations in OpenAlex.

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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 9 institutions in 3 countries.

Sandra W JacobsonDepartment of Psychiatry and Behavioral Neurosciences , Wayne State University School of Medicine, Detroit, Michigan.ORCID http://orcid.org/0000-0002-9768-2671
Joseph L JacobsonDepartment of Psychiatry and Behavioral Neurosciences , Wayne State University School of Medicine, Detroit, Michigan.
Christopher D MoltenoDepartment of Psychiatry and Mental Health , Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Christopher M R WartonDepartment of Human Biology , Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Pia WintermarkMontreal Children's Hospital , Montreal, Quebec, Canada.
H Eugene HoymeDepartment of Pediatrics , Sanford School of Medicine, University of South Dakota, Sioux Falls, South Dakota.
Greetje De JongDivision of Molecular Biology and Human Genetics , Stellenbosch University, Faculty of Medicine and Health Sciences, Cape Town, South Africa.
Paul TaylorDepartment of Human Biology , Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Fleur WartonDepartment of Human Biology , Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
Nadine M LindingerDepartment of Psychology , University of Cape Town, Cape Town, South Africa.
R Colin CarterDivision of Pediatric Emergency Medicine , Morgan Stanley Children's Hospital of New York, Columbia University Medical Center, New York, New York.ORCID http://orcid.org/0000-0003-1554-6914
Neil C DodgeDepartment of Psychiatry and Behavioral Neurosciences , Wayne State University School of Medicine, Detroit, Michigan.
Ellen GrantDivision of Pediatric Emergency Medicine , Morgan Stanley Children's Hospital of New York, Columbia University Medical Center, New York, New York.
Simon K WarfieldDepartment of Pediatrics , Boston Children's Hospital/Harvard Medical School, Boston, Massachusetts.
Lilla ZölleiDepartment of Radiology , Massachusetts General Hospital, Boston, Massachusetts.
André J W van der KouweDepartment of Radiology , Massachusetts General Hospital, Boston, Massachusetts.
Ernesta M MeintjesDepartment of Human Biology , Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.
University of Cape Town · ZAMassachusetts General Hospital · USMorgan Stanley Children's Hospital · USBoston Children's Hospital · USMontreal Children's Hospital · CANational Institutes of Health · USStellenbosch University · ZAUniversity of Arizona · USWayne State University · US

Funding

Scientific and Statistical Computing CoreZICMH002888 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI TAYLOR, PAUL · 2009 to 2025
$30.9M
Image Analysis of Neurofacial Effects of Prenatal AlcoholExposureU01AA014809 · NIAAA · UNIVERSITY OF OXFORD · PI Michael Suttie · 2007 to 2026
$5.8M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI POMEROY, SCOTT LOREN · 2016 to 2020
$5.2M
Neural Bases of Eyeblink Conditioning in FASDR01AA016781 · NIAAA · WAYNE STATE UNIVERSITY · PI JACOBSON, SANDRA W. · 2008 to 2012
$2.5M
Brain Imaging of Newborns with Fetal Alcohol SyndromeR21AA020037 · NIAAA · WAYNE STATE UNIVERSITY · PI JACOBSON, SANDRA W., MEINTJES, ERNESTA MARIA · 2011 to 2012
$485k
NIAAA NIH HHS R01 AA016781NIAAA NIH HHS R21 AA020037NIAAA NIH HHS U01 AA014809NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

backgroundMagnetic resonance imaging (MRI) studies have consistently demonstrated disproportionately smaller corpus callosa in individuals with a history of prenatal alcohol exposure (PAE) but have not previously examined the feasibility of detecting this effect in infants. Tissue segmentation of the newborn brain is challenging because analysis techniques developed for the adult brain are not directly transferable, and segmentation for cerebral morphometry is difficult in neonates, due to the latter's incomplete myelination. This study is the first to use volumetric structural MRI to investigate PAE effects in newborns using manual tracing and to examine the cross-sectional area of the corpus callosum (CC).

methodsForty-three nonsedated infants born to 32 Cape Coloured heavy drinkers and 11 controls recruited prospectively during pregnancy were scanned using a custom-designed birdcage coil for infants, which increases signal-to-noise ratio almost 2-fold compared to the standard head coil. Alcohol use was ascertained prospectively during pregnancy, and fetal alcohol spectrum disorders diagnosis was conducted by expert dysmorphologists. Data were acquired using a multi-echo FLASH protocol adapted for newborns, and a knowledge-based procedure was used to hand-segment the neonatal brains.

resultsCC was disproportionately smaller in alcohol-exposed neonates than controls after controlling for intracranial volume. By contrast, CC area was unrelated to infant sex, gestational age, age at scan, or maternal smoking, marijuana, or methamphetamine use during pregnancy.

conclusionsGiven that midline craniofacial anomalies have been recognized as a hallmark of fetal alcohol syndrome in humans and animal models since this syndrome was first identified, the CC deficit identified here in newborns may support early identification of a range of midline structural impairments. Smaller CC during the newborn period may provide an early indicator of fetal alcohol-related cognitive deficits that have been linked to this critically important brain structure in childhood and adolescence.

Indexed as

Magnetic Resonance ImagingAdultAlcohol DrinkingCorpus CallosumFemaleHumansInfant, NewbornLongitudinal StudiesMalePregnancyPrenatal Exposure Delayed EffectsSouth AfricaYoung AdultCorpus CallosumFetal Alcohol Spectrum DisordersFetal Alcohol SyndromeManual TracingNeonatal Brain MRIPrenatal Alcohol Exposure

Identifiers

PMID28247416
PMCPMC5404976
OpenAlexW2592783968

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.