Evidence map›Paper›PMID 28346058›Full record

ReviewPharmacogenomics2017

Promising pharmacogenetic targets for treating alcohol use disorder: evidence from preclinical models.

Jennifer A Rinker, Patrick J Mulholland

Open access · greenAbstract readReview
In one paragraph

Review in Pharmacogenomics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.0field-weighted citation impact, top 10% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Kv7 Channels and Excitability Disorders.Handbook of experimental pharmacology · 2021
    Article
  6. Article
  7. Article
  8. Pharmacogenetics of alcohol addiction: current perspectives.The application of clinical genetics · 2019
    Article
  9. Psoriasis and alcohol.Psoriasis (Auckland, N.Z.) · 2019
    Article
  10. Article
  11. Article
  12. 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

2 authors at 1 institution in 1 country.

Jennifer A RinkerDepartment of Neuroscience, Medical University of South Carolina, Charleston, SC 29425, USA.
Patrick J MulhollandDepartment of Neuroscience, Medical University of South Carolina, Charleston, SC 29425, USA.
Medical University of South Carolina · US

Funding

TREATING ETHANOL WITHDRAWAL WITH LORAZEPAM/NALTREXONEP50AA010761 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI Patrick J. Mulholland · 1996 to 2026
$46.8M
Kv7 channels and heavy alcohol drinkingR01AA023288 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MULHOLLAND, PATRICK J. · 2014 to 2023
$3.4M
Stress and Ethanol Dependence: SK Channels and GlutamateU01AA020930 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI MULHOLLAND, PATRICK J. · 2012 to 2021
$2.6M
Dependence-Induced Excessive Ethanol Consumption: Role of Corticostriatal Kv7 ChannelsK01AA025110 · NIAAA · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RINKER, JENNIFER ANNE · 2017 to 2021
$930k
Role of BDNF in Stress Effects on Ethanol Dependence-Induced Escalated DrinkingI01BX000813 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI BECKER, HOWARD C. · 2011 to 2024
–
NIAAA NIH HHS K01 AA025110NIAAA NIH HHS P50 AA010761NIAAA NIH HHS R01 AA023288NIAAA NIH HHS U01 AA020930
6 · The paper itself

Abstract

Inherited genetic variants contribute to risk factors for developing an alcohol use disorder, and polymorphisms may inform precision medicine strategies for treating alcohol addiction. Targeting genetic mutations linked to alcohol phenotypes has provided promising initial evidence for reducing relapse rates in alcoholics. Although successful in some studies, there are conflicting findings and the reports of adverse effects may ultimately limit their clinical utility, suggesting that novel pharmacogenetic targets are necessary to advance precision medicine approaches. Here, we describe promising novel genetic variants derived from preclinical models of alcohol consumption and dependence that may uncover disease mechanisms that drive uncontrolled drinking and identify novel pharmacogenetic targets that facilitate therapeutic intervention for the treatment of alcohol use disorder.

Indexed as

Models, AnimalPharmacogenomic TestingPharmacogenomic VariantsPolymorphism, Single NucleotideAlcohol-Related DisordersAnimalsHumansMutationNeuroimmunomodulationPotassium ChannelsPrecision MedicinePotassium Channelsalcohol use disorderK+ channelsneuroimmune genespharmacogeneticspreclinical modelsRAS signalingtachykinins

Identifiers

PMID28346058
PMCPMC5558539
OpenAlexW2598516583

What OpenQuestion holds

Textmetadata
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.