Evidence map›Paper›PMID 29881439›Full record

ArticleAnnals of general psychiatry2018

The frequency of

Hiba Alblooshi, Gary Hulse, Wael Osman, Ahmed El Kashef, Mansour Shawky, Hamad Al Ghaferi, Habiba Al Safar, Guan K Tay

Open access · goldAbstract read
In one paragraph

Article in Annals of general psychiatry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 38% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Pharmacogenetic Approach to Tramadol Use in the Arab Population.International journal of molecular sciences · 2024
    Article
  4. Article
  5. Genetic Vulnerability to Opioid Addiction.Cold Spring Harbor perspectives in medicine · 2021
    Review
  6. Article
  7. 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

8 authors at 4 institutions in 2 countries.

Hiba Alblooshi1School of Human Sciences, The University of Western Australia, Crawley, WA Australia.
Gary Hulse2School of Psychiatry and Clinical Neurosciences, The University of Western Australia, Crawley, WA Australia.
Wael Osman4Center of Biotechnology, Khalifa University of Science, Technology and Research, PO Box 1227788, Abu Dhabi, United Arab Emirates.
Ahmed El KashefUnited Arab Emirates National Rehabilitation Center, Abu Dhabi, United Arab Emirates.
Mansour ShawkyUnited Arab Emirates National Rehabilitation Center, Abu Dhabi, United Arab Emirates.
Hamad Al GhaferiUnited Arab Emirates National Rehabilitation Center, Abu Dhabi, United Arab Emirates.
Habiba Al Safar4Center of Biotechnology, Khalifa University of Science, Technology and Research, PO Box 1227788, Abu Dhabi, United Arab Emirates.
Guan K Tay2School of Psychiatry and Clinical Neurosciences, The University of Western Australia, Crawley, WA Australia.ORCID 0000-0001-6639-3298
Emirates Foundation · AEEdith Cowan University · AUKhalifa University of Science and Technology · AEThe University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDopaminergic and opioid systems are involved in mediating drug reward and reinforcement of various types of substances including psychoactive compounds. Genes of both systems have been candidate for investigation for associations with substance use disorder (SUD) in various populations. This study is the first study to determine the allele frequency and the genetic association of the

methodsA cross-sectional case-control cohort that consisted of 512 male subjects was studied. Two hundred and fifty patients with SUD receiving treatment at the UAE National Rehabilitation Center were compared to 262 controls with no prior history of mental health and SUD. DNA from each subject was extracted and genotyped using the TaqMan

resultsThere were no significant associations observed for

conclusionFurther research is required with refinements to the criteria of the clinical phenotypes. Genetic studies have to be expanded to include other variants of the gene, the interaction with other genes, and possible epigenetic relationships.

Indexed as

DRD2 geneOPRM1 geners1076560rs1799971Substance use disorderUAE

Identifiers

PMID29881439
PMCPMC5984335
OpenAlexW2807688763

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.