Evidence map›Paper›PMID 39684228›Full record

ArticleInternational journal of molecular sciences2024

Genetic Variants Linked to Opioid Addiction: A Genome-Wide Association Study.

Shailesh Kumar Panday, Vijay Shankar, Rachel Ann Lyman, Emil Alexov

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Opioid dependence in patients with pain in chronic pancreatitis an emerging problem.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2025
    Review
  4. Interaction BetweenNeurology international · 2025
    Article
  5. Review
  6. Review
  7. Article
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

4 authors.

Shailesh Kumar PandayDepartment of Physics and Astronomy, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0003-3099-8679
Vijay ShankarCenter for Human Genetics, Clemson University, Greenwood, SC 29646, USA.ORCID 0000-0001-9001-5748
Rachel Ann LymanCenter for Human Genetics, Clemson University, Greenwood, SC 29646, USA.
Emil AlexovDepartment of Physics and Astronomy, Clemson University, Clemson, SC 29634, USA.ORCID 0000-0001-5346-0156

Funding

Statistical Methods for Gene Regulatory Analysis From Single Cell Genomics DataP20GM139769 · NIGMS · CLEMSON UNIVERSITY · PI ANHOLT, ROBERT R. H, ARNO, GAVIN · 2021 to 2025
$10.8M
New Generation DelPhi: large systems and beyond electrostaticsR01GM093937 · NIGMS · CLEMSON UNIVERSITY · PI ALEXOV, EMIL GEORGIEV · 2010 to 2023
$4.3M
DelPhi and associated resources: maintenance, development and applicationsR35GM151964 · NIGMS · CLEMSON UNIVERSITY · PI Emil Georgiev Alexov · 2024 to 2026
$1.1M
NIGMS NIH HHS P20 GM139769NIGMS NIH HHS R01 GM093937NIGMS NIH HHS R35 GM151964NIH HHS R35GM151964
6 · The paper itself

Abstract

Opioid use disorder (OUD) affects millions of people worldwide. While it is known that OUD originates from many factors, including social and environmental factors, the role of genetic variants in developing the disease has also been reported. This study aims to investigate the genetic variants associated with the risk of developing OUD upon exposure. Twenty-three subjects who had previously been given opioid-based painkillers to undergo minor surgical treatment were recruited at Prisma Health Upstate clinic and elsewhere. Eleven were considered nonpersistent opioid users (controls), and 12 were persistent opioid users (cases) at the time of sample collection after an initial surgery. The subjects were asked to provide saliva samples, which were subjected to DNA sequencing at Clemson University Center for Human Genetics, and variant calling was performed. The genome-wide association studies (GWASs) for genes known to be associated with OUD resulted in 13 variants (intronic or SNV) with genome-wide significance (raw

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyOpioid-Related DisordersPolymorphism, Single NucleotideAdultFemaleGenetic VariationHumansMaleMiddle AgedReceptors, Opioid, muOPRM1 protein, humanReceptors, Opioid, mucase-control genome-wide association studyfunctional enrichment analysisgenetic variantsprotein–protein interaction network

Identifiers

PMID39684228
PMCPMC11641826

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.