Evidence map›Paper›PMID 23976958›Full record

ArticlePloS one2013

Dopamine D1 receptor gene variation modulates opioid dependence risk by affecting transition to addiction.

Feng Zhu, Chun-xia Yan, Yi-chong Wen, Jiayin Wang, Jinbo Bi, Ya-ling Zhao, Lai Wei, Cheng-ge Gao, Wei Jia, Sheng-bin Li

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

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  14. DRD1 and DRD2 genotypes modulate processing modes of goal activation processes during action cascading.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
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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

10 authors at 6 institutions in 2 countries.

Feng ZhuCollege of Medicine and Forensics, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi, People's Republic of China ; Key Laboratory of the Health Ministry for Forensic Sciences, Xi'an Jiaotong University, Xi'an, Shaanxi, People's Republic of China ; Key Laboratory of the Education Ministry for Environment and Genes Related to Diseases, Xi'an, Shaanxi, People's Republic of China.
Chun-xia Yan
Yi-chong Wen
Jiayin Wang
Jinbo Bi
Ya-ling Zhao
Lai Wei
Cheng-ge Gao
Wei Jia
Sheng-bin Li
Ministry of Education of the People's Republic of China · CNXi'an Jiaotong University · CNFirst Affiliated Hospital of Xi'an Jiaotong University · CNUConn Health · USWashington University in St. Louis · USXian Mental Health Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dopamine D1 receptor (DRD1) modulates opioid reinforcement, reward, and opioid-induced neuroadaptation. We propose that DRD1 polymorphism affects susceptibility to opioid dependence (OD), the efficiency of transition to OD, and opioid-induced pleasure response. We analyzed potential association between seven DRD1 polymorphisms with the following traits: duration of transition from the first use to dependence (DTFUD), subjective pleasure responses to opioid on first use and post-dependence use, and OD risk in 425 Chinese with OD and 514 healthy controls. DTFUD and level of pleasure responses were examined using a semi-structured interview. The DTFUD of opioid addicts ranged from 5 days to 11 years. Most addicts (64.0%) reported non-comfortable response upon first opioid use, while after dependence, most addicts (53.0%) felt strong opioid-induced pleasure. Survival analysis revealed a correlation of prolonged DTFUD with the minor allele-carrying genotypes of DRD1 rs4532 (hazard ratios (HR) = 0.694; p = 0.001) and rs686 (HR = 0.681, p = 0.0003). Binary logistic regression indicated that rs10063995 GT genotype (vs. GG+TT, OR = 0.261) could predict decreased pleasure response to first-time use and the minor alleles of rs686 (OR = 0.535) and rs4532 (OR = 0.537) could predict decreased post-dependence pleasure. Moreover, rs686 minor allele was associated with a decreased risk for rapid transition from initial use to dependence (DTFUD≤30 days; OR = 0.603) or post-dependence euphoria (OR = 0.603) relative to major allele. In conclusion, DRD1 rs686 minor allele decreases the OD risk by prolonging the transition to dependence and attenuating opioid-induced pleasure in Chinese.

Indexed as

Polymorphism, Single NucleotideAdultAge of OnsetAllelesBehavior, AddictiveCase-Control StudiesChinaFemaleHumansLogistic ModelsMaleOpioid-Related DisordersReceptors, Dopamine D1RiskSurveys and QuestionnairesTime FactorsDRD1 protein, humanReceptors, Dopamine D1

Identifiers

PMID23976958
PMCPMC3745389
OpenAlexW2076400706

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.