Evidence map›Paper›PMID 25175539›Full record

ArticleNeuroImage2014

Prenatal alcohol exposure reduces magnetic susceptibility contrast and anisotropy in the white matter of mouse brains.

Wei Cao, Wei Li, Hui Han, Shonagh K O'Leary-Moore, Kathleen K Sulik, G Allan Johnson, Chunlei Liu

Abstract read
In one paragraph

Article in NeuroImage, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.7field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

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  12. Effects of prenatal alcohol exposure (PAE): insights into FASD using mouse models of PAE.Biochemistry and cell biology = Biochimie et biologie cellulaire · 2018
    Review
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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

7 authors at 3 institutions in 2 countries.

Wei CaoBrain Imaging and Analysis Center, Duke University, Durham, NC, United States; Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Wei LiBrain Imaging and Analysis Center, Duke University, Durham, NC, United States.
Hui HanBrain Imaging and Analysis Center, Duke University, Durham, NC, United States.
Shonagh K O'Leary-MooreBowles Center for Alcohol Studies, University of North Carolina, Chapel Hill, NC, United States.
Kathleen K SulikBowles Center for Alcohol Studies, University of North Carolina, Chapel Hill, NC, United States.
G Allan JohnsonCenter for In Vivo Microscopy, Duke University, Durham, NC, United States.
Chunlei LiuBrain Imaging and Analysis Center, Duke University, Durham, NC, United States; Department of Radiology, Duke University, Durham, NC, United States. Electronic address: chunlei.liu@duke.edu.
Duke University · USUniversity of North Carolina at Chapel Hill · USHuazhong University of Science and Technology · CN

Funding

UNC ARC Information/Dissemination CoreP60AA011605 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Melissa A Herman · 2003 to 2026
$46.3M
INTEGRATED CENTER FOR IN VIVO MICROSCOPYP41EB015897 · NIBIB · DUKE UNIVERSITY · PI JOHNSON, GEORGE ALLAN · 2012 to 2017
$7.4M
Exploring the Genetics of FASD in Complementary Mouse and Fish ModelsU01AA021651 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI EBERHART, JOHANN K, PARNELL, SCOTT · 2012 to 2021
$3.2M
Ultra-Resolution Imaging of Brain Circuitry and its Development in Mental HealthR01MH096979 · NIMH · UNIVERSITY OF CALIFORNIA BERKELEY · PI LIU, CHUNLEI · 2013 to 2017
$1.8M
MAGNETIC RESONANCE AND DIFFUSION TENSOR IMAGING OF A MOUSE FASD MODEL U01U01AA017124 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SULIK, KATHLEEN K · 2007 to 2011
$1.2M
NIAAA NIH HHS P60 AA011605NIAAA NIH HHS P60-AA011605NIAAA NIH HHS U01 AA017124NIAAA NIH HHS U01-AA017124NIAAA NIH HHS U01 AA021651NIAAA NIH HHS U01-AA021651NIBIB NIH HHS P41 EB015897NIBIB NIH HHS P41EB015897NIMH NIH HHS R01 MH096979NIMH NIH HHS R01MH096979
6 · The paper itself

Abstract

Prenatal alcohol exposure can result in long-term cognitive and behavioral deficits. Fetal alcohol spectrum disorder (FASD) refers to a range of permanent birth defects caused by prenatal alcohol exposure, and is the most common neurodevelopmental disorder in the US. Studies by autopsy and conventional structural MRI indicate that the midline structures of the brain are particularly vulnerable to prenatal alcohol exposure. Diffusion tensor imaging (DTI) has shown that abnormalities in brain white matter especially the corpus callosum are very common in FASD. Quantitative susceptibility mapping (QSM) is a novel technique that measures tissue's magnetic property. Such magnetic property is affected by tissue microstructure and molecular composition including that of myelin in the white matter. In this work, we studied three major white matter fiber bundles of a mouse model of FASD and compared it to control mice using both QSM and DTI. QSM revealed clear and significant abnormalities in anterior commissure, corpus callosum, and hippocampal commissure, which were likely due to reduced myelination. Our data also suggested that QSM may be even more sensitive than DTI for examining changes due to prenatal alcohol exposure. Although this is a preclinical study, the technique of QSM is readily translatable to human brain.

Indexed as

Diffusion Tensor ImagingAnimalsAnisotropyBrainFemaleFetal Alcohol Spectrum DisordersMiceMice, Inbred C57BLSensitivity and SpecificityWhite MatterDTIFASDMagnetic susceptibility anisotropyQuantitative susceptibility mappingWhite matter

Identifiers

PMID25175539
PMCPMC4252734
OpenAlexW2091501154

What OpenQuestion holds

Textmetadata
LicenceTDM
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.