Risk Assessment for Heroin Use and Craving Score Using Polygenic Risk Score

被引:7
|
作者
Huang, Chieh-Liang [1 ,2 ]
Chen, Ping-Ho [3 ,4 ]
Lane, Hsien-Yuan [5 ,6 ,7 ,8 ]
Ho, Ing-Kang [2 ,9 ]
Chung, Chia-Min [8 ,9 ]
机构
[1] Minist Hlth & Welf, Tsaotun Psychiat Ctr, Nan Tou 54249, Taiwan
[2] China Med Univ, Coll Med, PhD Program Aging, Taichung 40402, Taiwan
[3] Kaohsiung Med Univ, Coll Dent Med, Sch Dent, Kaohsiung 80708, Taiwan
[4] Natl Sun Yat Sen Univ, Inst Biomed Sci, Kaohsiung 80424, Taiwan
[5] China Med Univ Hosp, Dept Psychiat, Taichung 40402, Taiwan
[6] China Med Univ Hosp, Brain Dis Res Ctr, Taichung 40402, Taiwan
[7] Asia Univ, Coll Med & Hlth Sci, Dept Psychol, Taichung 41354, Taiwan
[8] China Med Univ, Grad Inst Biomed Sci, Taichung 406040, Taiwan
[9] China Med Univ Hosp, Ctr Drug Abuse & Addict, Taichung 406040, Taiwan
来源
JOURNAL OF PERSONALIZED MEDICINE | 2021年 / 11卷 / 04期
关键词
genetic biomarker; addiction; craving; heroin;
D O I
10.3390/jpm11040259
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Addiction is characterized by drug-craving, compulsive drug-taking, and relapse, and results from the interaction between multiple genetic and environmental factors. Reward pathways play an important role in mediating drug-seeking and drug-taking behaviors, and relapse. The objective of this study was to identify heroin addicts who carry specific genetic variants in their dopaminergic reward systems. A total of 326 heroin-dependent patients undergoing methadone maintenance therapy (MMT) were recruited from the Addiction Center of the China Medical University Hospital. A heroin-use and craving questionnaire was used to evaluate the urge for heroin, the daily or weekly frequency of heroin usage, daily life disturbance, anxiety, and the ability to overcome heroin use. A general linear regression model was used to assess the associations of genetic polymorphisms in one's dopaminergic reward system with heroin-use and craving scores. Results: The most significant results were obtained for rs2240158 in GRIN3B (p = 0.021), rs3983721 in GRIN3A (p = 0.00326), rs2129575 in TPH2 (p = 0.033), rs6583954 in CYP2C19 (p = 0.033), and rs174699 in COMT (p = 0.036). These were all associated with heroin-using and craving scores with and without adjustments for age, sex, and body mass index. We combined five variants, and the ensuing dose-response effect indicated that heroin-craving scores increased with the numbers of risk alleles (p for trend = 0.0008). These findings will likely help us to understand the genetic mechanism of craving, which will help in predicting the risk of relapse in clinical practice and the potential for therapies to target craving in heroin addiction.
引用
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页数:7
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