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阿片类药物依赖易感性的遗传关联分析。

An analysis of genetic association in opioid dependence susceptibility.

作者信息

Nagaya D, Zahari Z, Saleem M, Yahaya B H, Tan S C, Yusoff N M

机构信息

Cluster for Regenerative Medicine, Advanced Medical and Dental Institute, Universiti Sains Malaysia, Minden, Penang, Malaysia.

Penang Medical College, George Town, Penang, Malaysia.

出版信息

J Clin Pharm Ther. 2018 Feb;43(1):80-86. doi: 10.1111/jcpt.12585. Epub 2017 Jun 27.

Abstract

WHAT IS KNOWN

Drug addiction is a novelty-seeking personality trait that is associated with the candidate genes OPRD1 (opioid delta receptors), OPRK1 (opioid kappa receptors) and PDYN (prodynorphin). However, associations between single nucleotide polymorphisms (SNPs) rs1042114 (80G>T) of the OPRD1 gene, rs702764 (843 A>G) of the OPRK1 gene, and rs910080 (3' UTR _743T>C), rs1997794 (5' UTR -381A>G) and rs1022563 (3' UTR) of the PDYN gene and novelty seeking remain controversial as reported results have not been reproducible.

OBJECTIVE

The goal of this study was to determine the frequencies of SNPs rs1042114, rs702764, rs1997794, rs1022563 and rs910080 in the Malaysian population and to study their association with opioid dependence in Malaysian Malays.

METHODS

A total of 459 Malay male with opioid dependence and 543 healthy male (controls) subjects were included in this study. SNPs were genotyped using the TaqMan SNP genotyping assay. Statistical analysis was performed using Golden Helix SVS software suite to identify the distribution of allele and genotype frequencies, and SNP-SNP interactions were also analysed in this study.

RESULTS AND DISCUSSION

SNP rs1042114 in the OPRD1 gene is strongly associated with opiate addiction (P=.0001). In individuals homozygous for this risk allele, the likelihood of opiate addiction is increased by a factor 1.62 (95% confidence interval (CI) 1.412-1.875). Polymorphic alleles at SNP rs702764 of OPRK1 were not associated with opioid dependence. A significant association between opioid dependence and SNP rs910080 of PDYN (P=.0217) was detected, but there was no association for SNPs rs199774 and rs1022563. A significant interaction was also identified between homozygous wild-type genotype TT of rs702764 with the risk genotypes TG/GG of rs1042114 (odds ratio (OR)=2.111 (95% CI 1.227-3.631), P=.0069) and with the risk genotypes GA/AA of rs910080 (OR=1.415 (95% CI 1.04-1.912), P=.0239).

WHAT IS NEW AND CONCLUSION

The results indicate that SNPs rs1042114 and rs910080 contribute to vulnerability to opioid dependence in the Malaysian Malay population. These results will help us to understand the effect of the SNPs and the SNP-SNP interaction on opioid dependence and may assist in efforts to screen vulnerable individuals and match them with individually tailored prevention and treatment strategies.

摘要

已知信息

药物成瘾是一种寻求新奇的人格特质,与候选基因OPRD1(阿片δ受体)、OPRK1(阿片κ受体)和PDYN(前强啡肽)相关。然而,据报道,OPRD1基因的单核苷酸多态性(SNP)rs1042114(80G>T)、OPRK1基因的rs702764(843 A>G)以及PDYN基因的rs910080(3'UTR_743T>C)、rs1997794(5'UTR -381A>G)和rs1022563(3'UTR)与寻求新奇之间的关联仍存在争议,因为报道的结果无法重现。

目的

本研究的目的是确定马来西亚人群中SNP rs1042114、rs702764、rs1997794、rs1022563和rs910080的频率,并研究它们与马来西亚马来人阿片类药物依赖的关联。

方法

本研究共纳入459名有阿片类药物依赖的马来男性和543名健康男性(对照组)。使用TaqMan SNP基因分型检测法对SNP进行基因分型。使用Golden Helix SVS软件套件进行统计分析,以确定等位基因和基因型频率的分布,本研究还分析了SNP-SNP相互作用。

结果与讨论

OPRD1基因中的SNP rs1042114与阿片类药物成瘾密切相关(P = 0.0001)。在该风险等位基因的纯合个体中,阿片类药物成瘾的可能性增加了1.62倍(95%置信区间(CI)1.412 - 1.875)。OPRK1的SNP rs702764的多态性等位基因与阿片类药物依赖无关。检测到阿片类药物依赖与PDYN的SNP rs910080之间存在显著关联(P = 0.0217),但SNP rs199774和rs1022563无关联。还发现rs702764的纯合野生型基因型TT与rs1042114的风险基因型TG/GG(优势比(OR)= 2.111(95% CI 1.227 - 3.631),P = 0.0069)以及与rs910080的风险基因型GA/AA(OR = 1.415(95% CI 1.04 - 1.912),P = 0.0239)之间存在显著相互作用。

新发现与结论

结果表明,SNP rs1042114和rs910080导致马来西亚马来人群体易患阿片类药物依赖。这些结果将有助于我们了解SNP以及SNP-SNP相互作用对阿片类药物依赖的影响,并可能有助于筛查易患个体并为他们匹配个性化定制的预防和治疗策略。

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