Evidence map›Paper›PMID 38746311›Full record

ArticlebioRxiv : the preprint server for biology2024

Divergent gene expression patterns in alcohol and opioid use disorders lead to consistent alterations in functional networks within the Dorsolateral Prefrontal Cortex.

Martha MacDonald, Pablo A S Fonseca, Kory Johnson, Erin M Murray, Rachel L Kember, Henry Kranzler, Dayne Mayfield, Daniel da Silva

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Martha MacDonaldNash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY.
Pablo A S FonsecaDpto. Producción Animal, Facultad de Veterinaria, Universidad de León. Campus de Vegazana s/n, 24007 Leon, Spain.
Kory JohnsonBioinformatics Section, Intramural Information Technology & Bioinformatics Program, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD.
Erin M MurrayDepartment of Neuroscience, University of Rochester School of Medicine, Rochester NY.
Rachel L KemberCenter for Studies of Addiction, University of Pennsylvania, Perelman School of Medicine and Mental Illness Research, Education and Clinical Center, Crescenz VAMC, Philadelphia, PA, USA.
Henry KranzlerCenter for Studies of Addiction, University of Pennsylvania, Perelman School of Medicine and Mental Illness Research, Education and Clinical Center, Crescenz VAMC, Philadelphia, PA, USA.
Dayne MayfieldDepartment of Neuroscience Waggoner Center for Alcohol and Addiction Research, The University of Texas at Austin, Austin, TX.
Daniel da SilvaNash Family Department of Neuroscience, Icahn School of Medicine at Mount Sinai, New York, NY.

Funding

Conduits: Mount Sinai Health System Translational Science HubUL1TR004419 · NCATS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Rosalind J Wright · 2022 to 2026
$46.4M
Characterizing the phenotypic spectrum associated with genetic liability for alcohol use disorderK01AA028292 · NIAAA · UNIVERSITY OF PENNSYLVANIA · PI KEMBER, RACHEL LORRAINE · 2021 to 2024
$505k
Genetic Vulnerability for Sustained Multi-Substance Use in MVPI01BX004820 · VA · VA CONNECTICUT HEALTHCARE SYSTEM · PI Amy Caroline Justice, HENRY RICHARD KRANZLER · 2020 to 2026
–
BLRD VA I01 BX004820NCATS NIH HHS UL1 TR004419NIAAA NIH HHS K01 AA028292
6 · The paper itself

Abstract

Substance Use Disorders (SUDs) manifest as persistent drug-seeking behavior despite adverse consequences, with Alcohol Use Disorder (AUD) and Opioid Use Disorder (OUD) representing prevalent forms associated with significant mortality rates and economic burdens. The co-occurrence of AUD and OUD is common, necessitating a deeper comprehension of their intricate interactions. While the causal link between these disorders remains elusive, shared genetic factors are hypothesized. Leveraging public datasets, we employed genomic and transcriptomic analyses to explore conserved and distinct molecular pathways within the dorsolateral prefrontal cortex associated with AUD and OUD. Our findings unveil modest transcriptomic overlap at the gene level between the two disorders but substantial convergence on shared biological pathways. Notably, these pathways predominantly involve inflammatory processes, synaptic plasticity, and key intracellular signaling regulators. Integration of transcriptomic data with the latest genome-wide association studies (GWAS) for problematic alcohol use (PAU) and OUD not only corroborated our transcriptomic findings but also confirmed the limited shared heritability between the disorders. Overall, our study indicates that while alcohol and opioids induce diverse transcriptional alterations at the gene level, they converge on select biological pathways, offering promising avenues for novel therapeutic targets aimed at addressing both disorders simultaneously.

Identifiers

PMID38746311
PMCPMC11092658

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.