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Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence
BACKGROUND AND OBJECT: Whether opioid-receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) is associated with nicotine dependence is controversial. We analyzed the combined results from published studies of this possibility. METHODS: Literature reviews were performed according to Preferred Reporting...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663599/ https://www.ncbi.nlm.nih.gov/pubmed/29137427 http://dx.doi.org/10.18632/oncotarget.20939 |
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author | Kong, Xiangyi Deng, Hao Alston, Theodore Kong, Yanguo Wang, Jingping |
author_facet | Kong, Xiangyi Deng, Hao Alston, Theodore Kong, Yanguo Wang, Jingping |
author_sort | Kong, Xiangyi |
collection | PubMed |
description | BACKGROUND AND OBJECT: Whether opioid-receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) is associated with nicotine dependence is controversial. We analyzed the combined results from published studies of this possibility. METHODS: Literature reviews were performed according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Web of Science, Chinese National Science Infrastructure (CNKI), PubMed, Embase and Google Scholar database searches using MeSH terms were conducted to find all relevant researches up to October 2016. Odds ratios (ORs) and their 95% confidence intervals (95% CIs) were calculated in allele, homozygote, heterozygote, dominant and recessive models. Ethnicity-specific subgroup meta-analysis, heterogeneity, sensitivity analysis and publication bias were considered. RESULTS: Seven eligible studies with 3313 patients were included. The ORs in the five genetic models mentioned above were 1.000 (95% CI: 0.906, 1.104; p = 0.999), 1.032 (95% CI: 0.771, 1.381; p = 0.834), 0.963 (95% CI: 0.799, 1.162; p = 0.696), 1.006 (95% CI: 0.916, 1.104; p = 0.907), 0.967 (95% CI: 0.715, 1.309; p = 0.830), respectively. Only in dominant model is the association significant. Upon ethnicity-specific subgroup analysis, there is no statistical significance. CONCLUSION: OPRM1-A118G polymorphism (A>G) is not associated with nicotine dependence. |
format | Online Article Text |
id | pubmed-5663599 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56635992017-11-13 Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence Kong, Xiangyi Deng, Hao Alston, Theodore Kong, Yanguo Wang, Jingping Oncotarget Research Paper BACKGROUND AND OBJECT: Whether opioid-receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) is associated with nicotine dependence is controversial. We analyzed the combined results from published studies of this possibility. METHODS: Literature reviews were performed according to Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Web of Science, Chinese National Science Infrastructure (CNKI), PubMed, Embase and Google Scholar database searches using MeSH terms were conducted to find all relevant researches up to October 2016. Odds ratios (ORs) and their 95% confidence intervals (95% CIs) were calculated in allele, homozygote, heterozygote, dominant and recessive models. Ethnicity-specific subgroup meta-analysis, heterogeneity, sensitivity analysis and publication bias were considered. RESULTS: Seven eligible studies with 3313 patients were included. The ORs in the five genetic models mentioned above were 1.000 (95% CI: 0.906, 1.104; p = 0.999), 1.032 (95% CI: 0.771, 1.381; p = 0.834), 0.963 (95% CI: 0.799, 1.162; p = 0.696), 1.006 (95% CI: 0.916, 1.104; p = 0.907), 0.967 (95% CI: 0.715, 1.309; p = 0.830), respectively. Only in dominant model is the association significant. Upon ethnicity-specific subgroup analysis, there is no statistical significance. CONCLUSION: OPRM1-A118G polymorphism (A>G) is not associated with nicotine dependence. Impact Journals LLC 2017-09-15 /pmc/articles/PMC5663599/ /pubmed/29137427 http://dx.doi.org/10.18632/oncotarget.20939 Text en Copyright: © 2017 Kong et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Kong, Xiangyi Deng, Hao Alston, Theodore Kong, Yanguo Wang, Jingping Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence |
title | Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence |
title_full | Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence |
title_fullStr | Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence |
title_full_unstemmed | Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence |
title_short | Association of opioid receptor mu 1 (OPRM1) A118G polymorphism (rs1799971) with nicotine dependence |
title_sort | association of opioid receptor mu 1 (oprm1) a118g polymorphism (rs1799971) with nicotine dependence |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663599/ https://www.ncbi.nlm.nih.gov/pubmed/29137427 http://dx.doi.org/10.18632/oncotarget.20939 |
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