Evidence map›Paper›PMID 34702274›Full record

ArticleBMC medical genomics2021

Genetics and prescription opioid use (GaPO): study design for consenting a cohort from an existing biobank to identify clinical and genetic factors influencing prescription opioid use and abuse.

Vanessa Troiani, Richard C Crist, Glenn A Doyle, Thomas N Ferraro, Donielle Beiler, Stephanie Ranck, Kortney McBryan, Margaret A Jarvis, Jordan S Barbour, John J Han and 3 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

13 authors at 4 institutions in 1 country.

Vanessa TroianiGeisinger Clinic, Geisinger, Danville, PA, USA. vtroiani@geisinger.edu.ORCID 0000-0001-6689-8157
Richard C CristCenter for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Glenn A DoyleCenter for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Thomas N FerraroCenter for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Donielle BeilerGeisinger Clinic, Geisinger, Danville, PA, USA.
Stephanie RanckGeisinger Clinic, Geisinger, Danville, PA, USA.
Kortney McBryanGeisinger Clinic, Geisinger, Danville, PA, USA.
Margaret A JarvisGeisinger Clinic, Geisinger, Danville, PA, USA.
Jordan S BarbourGeisinger Clinic, Geisinger, Danville, PA, USA.
John J HanDepartment of Pain Medicine, Geisinger Medical Center, Danville, PA, USA.
Ryan J NessDepartment of Pain Medicine, Geisinger Medical Center, Danville, PA, USA.
Wade H BerrettiniGeisinger Clinic, Geisinger, Danville, PA, USA.
Janet D RobishawDepartment of Biomedical Science, Schmidt College of Medicine of Florida Atlantic University, Boca Raton, FL, USA.
Geisinger Medical Center · USUniversity of Pennsylvania · USCooper Medical School of Rowan University · USFlorida Atlantic University · 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
NIDA NIH HHS DA044015NIDA NIH HHS R01 DA044015
6 · The paper itself

Abstract

backgroundPrescription opioids (POs) are commonly used to treat moderate to severe chronic pain in the health system setting. Although they improve quality of life for many patients, more work is needed to identify both the clinical and genetic factors that put certain individuals at high risk for developing opioid use disorder (OUD) following use of POs for pain relief. With a greater understanding of important risk factors, physicians will be better able to identify patients at highest risk for developing OUD for whom non-opioid alternative therapies and treatments should be considered.

methodsWe are conducting a prospective observational study that aims to identify the clinical and genetic factors most stongly associated with OUD. The study design leverages an existing biobank that includes whole exome sequencing and array genotyping. The biobank is maintained within an integrated health system, allowing for the large-scale capture and integration of genetic and non-genetic data. Participants are enrolled into the health system biobank via informed consent and then into a second study that focuses on opioid medication use. Data capture includes validated self-report surveys measuring addiction severity, depression, anxiety, and nicotine use, as well as additional clinical, prescription, and brain imaging data extracted from electronic health records. DISCUSSION: We will harness this multimodal data capture to establish meaningful patient phenotypes in order to understand the genetic and non-genetic contributions to OUD.

Indexed as

Biological Specimen BanksAnalgesics, OpioidElectronic Health RecordsGenome-Wide Association StudyHumansOpioid-Related DisordersProspective StudiesAnalgesics, OpioidAddictionGeneticsOpioid use disorder (OUD)Substance misuse

Identifiers

PMID34702274
PMCPMC8547564
OpenAlexW3210234974

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.