Evidence map›Paper›PMID 36005827›Full record

ReviewNon-coding RNA2022

Long Non-Coding RNAs: The New Frontier into Understanding the Etiology of Alcohol Use Disorder.

Allie N Denham, John Drake, Matthew Gavrilov, Zachary N Taylor, Silviu-Alin Bacanu, Vladimir I Vladimirov

Open access · goldAbstract readReview
In one paragraph

Review in Non-coding RNA, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.9field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. The Role of miR-128 in Neurodegenerative Diseases.International journal of molecular sciences · 2023
    Review
  9. Review
  10. Review
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 3 institutions in 1 country.

Allie N DenhamDepartment of Psychiatry and Behavioral Sciences, Texas A&M University, Bryan, TX 77807, USA.
John DrakeDepartment of Psychiatry and Behavioral Sciences, Texas A&M University, Bryan, TX 77807, USA.ORCID 0000-0002-0420-3740
Matthew GavrilovDepartment of Psychiatry and Behavioral Sciences, Texas A&M University, Bryan, TX 77807, USA.
Zachary N TaylorDepartment of Psychiatry and Behavioral Sciences, Texas A&M University, Bryan, TX 77807, USA.
Silviu-Alin BacanuVirginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, VA 23219, USA.
Vladimir I VladimirovDepartment of Psychiatry and Behavioral Sciences, Texas A&M University, Bryan, TX 77807, USA.
University of Arizona · USTexas A&M University · USVirginia Commonwealth University · US

Funding

Assessing miRNA expression in the Corticolimbic System of Major Depressive DisorderR01MH118239 · NIMH · VIRGINIA COMMONWEALTH UNIVERSITY · PI VLADIMIROV, VLADIMIR IVANOV · 2019 to 2024
$2.8M
Using transmitted and untransmitted gene networks to identify molecular pathways to substance use & misuse in genetically controlled twinsR01DA052453 · NIDA · VIRGINIA COMMONWEALTH UNIVERSITY · PI GILLESPIE, NATHAN ALEXANDER, VLADIMIROV, VLADIMIR IVANOV · 2021 to 2024
$2.2M
Translational Approach to Studying miRNA functions in sACC and amygdala in patients with BPDR01MH132806 · NIMH · UNIVERSITY OF ARIZONA · PI Vladimir Ivanov Vladimirov · 2023 to 2026
$2.2M
Integrating miRNAs and mRNAs with alcohol eQTLs in two postmortem brain regionsR21AA022749 · NIAAA · VIRGINIA COMMONWEALTH UNIVERSITY · PI VLADIMIROV, VLADIMIR IVANOV · 2015 to 2016
$400k
NIAAA NIH HHS R21 AA022749NIAAA NIH HHS R21AA022749NIDA NIH HHS R01 DA052453NIDA NIH HHS R01DA052453NIMH NIH HHS R01 MH118239NIMH NIH HHS R01MH118239NIMH NIH HHS R01 MH132806
6 · The paper itself

Abstract

Alcohol use disorder (AUD) is a complex, chronic, debilitating condition impacting millions worldwide. Genetic, environmental, and epigenetic factors are known to contribute to the development of AUD. Long non-coding RNAs (lncRNAs) are a class of regulatory RNAs, commonly referred to as the "dark matter" of the genome, with little to no protein-coding potential. LncRNAs have been implicated in numerous processes critical for cell survival, suggesting that they play important functional roles in regulating different cell processes. LncRNAs were also shown to display higher tissue specificity than protein-coding genes and have a higher abundance in the brain and central nervous system, demonstrating a possible role in the etiology of psychiatric disorders. Indeed, genetic (e.g., genome-wide association studies (GWAS)), molecular (e.g., expression quantitative trait loci (eQTL)) and epigenetic studies from postmortem brain tissues have identified a growing list of lncRNAs associated with neuropsychiatric and substance use disorders. Given that the expression patterns of lncRNAs have been associated with widespread changes in the transcriptome, including methylation, chromatin architecture, and activation or suppression of translational activity, the regulatory nature of lncRNAs may be ubiquitous and an innate component of gene regulation. In this review, we present a synopsis of the functional impact that lncRNAs may play in the etiology of AUD. We also discuss the classifications of lncRNAs, their known functional roles, and therapeutic advancements in the field of lncRNAs to further clarify the functional relationship between lncRNAs and AUD.

Indexed as

alcohol use disorderlong non-coding RNAneuropsychiatric disorderspostmortem brain

Identifiers

PMID36005827
PMCPMC9415279
OpenAlexW4289942891

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.