Evidence map›Paper›PMID 24512105›Full record

ArticleAlcoholism, clinical and experimental research2014

Association between copy number variation losses and alcohol dependence across African American and European American ethnic groups.

Alvaro E Ulloa, Jiayu Chen, Victor M Vergara, Vince Calhoun, Jingyu Liu

Open access · greenAbstract read
In one paragraph

Article in Alcoholism, clinical and experimental research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
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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

5 authors at 2 institutions in 1 country.

Alvaro E UlloaElectrical and Computer Engineering Department, University of New Mexico, Albuquerque, New Mexico; The Mind Research Network and Lovelace Biomedical and Environmental Research Institute, Albuquerque, New Mexico.
Jiayu Chen
Victor M Vergara
Vince Calhoun
Jingyu Liu
Mind Research Network · USUniversity of New Mexico · US

Funding

A multilevel vulnerability study of substance abuse via CNV, brain activation andR33DA027626 · NIDA · THE MIND RESEARCH NETWORK · PI LIU, JINGYU · 2011 to 2012
$668k
NIDA NIH HHS R33 DA027626
6 · The paper itself

Abstract

backgroundCopy number variations (CNVs) are structural genetic mutations consisting of segmental gains or losses in DNA sequence. Although CNVs contribute substantially to genomic variation, few genetic and imaging studies report association of CNVs with alcohol dependence (AD). Our purpose is to find evidence of this association across ethnic populations and genders. This work is the first AD-CNV study across ethnic groups and the first to include the African American (AA) population.

methodsThis study considers 2 CNV data sets, one for discovery (2,345 samples) and the other for validation (239 samples), both including subjects with AD and healthy controls of European and African ancestry. Our analysis assesses the association between AD and CNV losses across ethnic groups and gender by examining the effect of overall losses across the whole genome, collective losses within individual cytogenetic bands, and specific losses in CNV regions.

resultsResults from the discovery data set showed an association between CNV losses within 16q12.2 and AD diagnosis (p = 4.53 × 10(-3) ). An overlapping CNV region from the validation data set exhibited the same direction of effect with respect to AD (p = 0.051). This CNV region affects the genes CES1p1 and CES1, which are members of the carboxylesterase (CES) family. The enzyme encoded by CES1 is a major liver enzyme that typically catalyzes the decomposition of ester into alcohol and carboxylic acid and is involved in drug or xenobiotics, fatty acid, and cholesterol metabolisms. In addition, the most significantly associated CNV region was located at 9p21.2 (p = 1.9 × 10(-3) ) in our discovery data set. Although not observed in the validation data set, probably due to small sample size, this result might hold potential connection to AD given its connection with neuronal death. In contrast, we did not find any association between AD and the overall total losses or the collective losses within individual cytogenetic bands.

conclusionsOverall, our study provides evidence that the specific CNVs at 16q12.2 contribute to the development of alcoholism in AA and European American populations.

Indexed as

AdultAlcoholismBlack or African AmericanCase-Control StudiesChromosomes, Human, Pair 16DNA Copy Number VariationsEthnicityGenome-Wide Association StudyGenotypeHumansMaleUnited StatesWhite PeopleAddictionAfrican AmericansAlcoholismCopy Number VariationEuropean Americans

Identifiers

PMID24512105
PMCPMC3999255
OpenAlexW2036087873

What OpenQuestion holds

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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.