Evidence map›Paper›PMID 27498914›Full record

ArticleActa neuropsychiatrica2017

Genetic variation within GRIN2B in adolescents with alcohol use disorder may be associated with larger left posterior cingulate cortex volume.

Shareefa Dalvie, Samantha J Brooks, Valerie Cardenas, George Fein, Raj Ramesar, Dan J Stein

Open access · greenAbstract read
In one paragraph

Article in Acta neuropsychiatrica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Article
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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

6 authors at 2 institutions in 2 countries.

Shareefa Dalvie1MRC/UCT Human Genetics Research Unit,Division of Human Genetics,Institute of Infectious Disease and Molecular Medicine,Faculty of Health Sciences,University of Cape Town,Observatory,Cape Town,South Africa.ORCID http://orcid.org/0000-0003-2333-4823
Samantha J Brooks2Department of Psychiatry and Mental Health,MRC Unit on Anxiety & Stress Disorders,University of Cape Town,Observatory,Cape Town,South Africa.
Valerie Cardenas3Neurobehavioral Research Inc.,Honolulu,HI,United States of America.
George Fein3Neurobehavioral Research Inc.,Honolulu,HI,United States of America.
Raj Ramesar1MRC/UCT Human Genetics Research Unit,Division of Human Genetics,Institute of Infectious Disease and Molecular Medicine,Faculty of Health Sciences,University of Cape Town,Observatory,Cape Town,South Africa.
Dan J Stein2Department of Psychiatry and Mental Health,MRC Unit on Anxiety & Stress Disorders,University of Cape Town,Observatory,Cape Town,South Africa.
University of Cape Town · ZANeurobehavioral Research (United States) · US

Funding

Effects of heavy alcohol abuse on adolescent brain structure and functionR01AA016303 · NIAAA · NEUROBEHAVIORAL RESEARCH, INC. · PI FEIN, GEORGE · 2007 to 2011
$2.8M
Cerebellar Structure and Function Studies in Very Early AbstinenceU01AA023674 · NIAAA · NEUROBEHAVIORAL RESEARCH, INC. · PI FEIN, GEORGE · 2015 to 2018
$1.4M
NIAAA NIH HHS R01 AA016303NIAAA NIH HHS U01 AA023674
6 · The paper itself

Abstract

objectiveBrain structure differences and adolescent alcohol dependence both show substantial heritability. However, exactly which genes are responsible for brain volume variation in adolescents with substance abuse disorders are currently unknown. The aim of this investigation was to determine whether genetic variants previously implicated in psychiatric disorders are associated with variation in brain volume in adolescents with alcohol use disorder (AUD).

methodsThe cohort consisted of 58 adolescents with DSM-IV AUD and 58 age and gender-matched controls of mixed ancestry ethnicity. An Illumina Infinium iSelect custom 6000 bead chip was used to genotype 5348 single nucleotide polymorphisms (SNPs) in 378 candidate genes. Magnetic resonance images were acquired and volumes of global and regional structures were estimated using voxel-based morphometry. To determine whether any of the genetic variants were associated with brain volume, association analysis was conducted using linear regression in Plink.

resultsFrom the exploratory analysis, the GRIN2B SNP rs219927 was associated with brain volume in the left posterior cingulate cortex (p<0.05), whereby having a G-allele was associated with a bigger volume.

conclusionThe GRIN2B gene is involved in glutamatergic signalling and may be associated with developmental differences in AUD in brain regions such as the posterior cingulate cortex. Such differences may play a role in risk for AUD, and deserve more detailed investigation.

Indexed as

AdolescentAlcoholismFemaleGyrus CinguliHumansMalePolymorphism, Single NucleotideReceptors, N-Methyl-D-AspartateNR2B NMDA receptorReceptors, N-Methyl-D-AspartateadolescentalcoholismGRIN2B receptormagnetic resonance imaging

Identifiers

PMID27498914
PMCPMC5478461
OpenAlexW2538838055

What OpenQuestion holds

Textmetadata
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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.