Evidence map›Paper›PMID 29302220›Full record

ReviewDialogues in clinical neuroscience2017

A brief review of the genetics and pharmacogenetics of opioid use disorders.

Wade Berrettini

Open access · diamondAbstract readReview
In one paragraph

Review in Dialogues in clinical neuroscience, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 3 pooled it
6.9field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 3 syntheses or guidelines pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Review
  6. Genetic and Epigenetic Approaches to Opioid Use Disorder.Expert reviews in molecular medicine · 2025
    Review
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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

1 author at 1 institution in 1 country.

Wade BerrettiniKarl E. Rickels Professor of Psychiatry, Perelman School of Medicine, University of Pennsylvania, USA.
University of Pennsylvania · US

Funding

Supplemental Application for Clinical and Genetic Risk Profile of Opioid Use DisorderR01DA044015 · NIDA · GEISINGER CLINIC · PI BERRETTINI, WADE H, ROBISHAW, JANET D · 2017 to 2021
$4.5M
Clinical and Genetic Characteristics of Opioid Addiction in Chronic PainR01DA032776 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI CHEATLE, MARTIN D · 2012 to 2016
$2.9M
Pharmacogenetics of Opioid Agonist TherapyR21DA036808 · NIDA · UNIVERSITY OF PENNSYLVANIA · PI BERRETTINI, WADE H · 2014 to 2015
$455k
NIDA NIH HHS R01 DA032776NIDA NIH HHS R01 DA044015NIDA NIH HHS R21 DA036808
6 · The paper itself

Abstract

Increased physician prescribing of opioids to treat chronic nonprogressive pain has been accompanied by an increase in opioid addiction. Twin studies of opioid addiction are consistent with an inherited component of risk, approximately 50%. Several genome-wide association study (GWAS) reports indicate that genetic risk for opioid addiction is conveyed by many alleles of small effect (odds ratios <1.5). These reports have detected alleles in potassium-ion-channel genes (

Indexed as

BuprenorphineCytochrome P-450 CYP2B6Genome-Wide Association StudyHumansNarcotic AntagonistsOpioid-Related DisordersPharmacogeneticsPolymorphism, Single NucleotidePotassium ChannelsReceptors, Opioid, muBuprenorphineCytochrome P-450 CYP2B6Narcotic AntagonistsPotassium ChannelsReceptors, Opioid, muaddictiondependencegeneticsopioidpharmacogenetics

Identifiers

PMID29302220
PMCPMC5741106
OpenAlexW2979494576

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.