The Role of Opioidergic Genes in the Treatment Outcome of Drug Addiction Pharmacotherapy: A Systematic Review

被引:28
作者
Bauer, Isabelle E. [1 ]
Soares, Jair C. [1 ]
Nielsen, David A. [2 ,3 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Psychiat & Behav Sci, Houston, TX 77030 USA
[2] Baylor Coll Med, Menninger Dept Psychiat & Behav Sci, Houston, TX 77030 USA
[3] Michael E DeBakey VA Med Ctr, Houston, TX USA
关键词
RECEPTOR GENE; NALTREXONE TREATMENT; ALCOHOL DEPENDENCE; HEAVY DRINKERS; DOUBLE-BLIND; OPRM1; POLYMORPHISMS; COCAINE; ASSOCIATION; MODERATORS;
D O I
10.1111/ajad.12172
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background and Objectives Drug addiction is a serious illness with deleterious functional and social consequences for both the affected individuals, their families, and society at large. In spite of the abundant research on substance dependence, there are few effective treatments for this disease. Given the crucial role of the endogenous opioid system in the development and maintenance of substance abuse disorders, this review focuses on the opioidergic system and examines the role of opioidergic genes in the treatment outcome of pharmacotherapies of alcohol, opioid, and cocaine addiction. Methods Scopus (all databases) and Pubmed were systematically searched with no language or year restrictions, up to July 2014, for studies that focused on the relationship between polymorphisms of opioidergic genes and the treatment outcome of pharmacotherapies of alcohol, opioid, and cocaine addictions. Selected search terms were opioid, gene, polymorphism, drug therapy, substance abuse, and response. Results and Conclusions The genetic variability of μ-, δ- and κ-opioid receptors genes OPRM1, OPRD1, and OPRK1 modulates the efficacy of opioid antagonist treatments such as naltrexone and methadone, as well as the cocaine vaccine. Despite the number of promising reports, data from additional cohorts are needed to substantiate these findings. Scientific Significance Gene variant profiling could help predict treatment response and assist in developing effective treatments for alcohol, opioid, and cocaine addiction. (Am J Addict 2015;24:15-23) © American Academy of Addiction Psychiatry.
引用
收藏
页码:15 / 23
页数:9
相关论文
共 51 条
  • [1] An evaluation of μ-opioid receptor (OPRM1) as a predictor of naltrexone response in the treatment of alcohol dependence
    Anton, Raymond F.
    Oroszi, Gabor
    O'Malley, Stephanie
    Couper, David
    Swift, Robert
    Pettinati, Helen
    Goldman, David
    [J]. ARCHIVES OF GENERAL PSYCHIATRY, 2008, 65 (02) : 135 - 144
  • [2] Naltrexone effects on alcohol consumption in a clinical laboratory paradigm: temporal effects of drinking
    Anton, RF
    Drobes, DJ
    Voronin, K
    Durazo-Avizu, R
    Moak, D
    [J]. PSYCHOPHARMACOLOGY, 2004, 173 (1-2) : 32 - 40
  • [3] Effects of opioid receptor gene variation on targeted nalmefene treatment in heavy drinkers
    Arias, Albert J.
    Armeli, Stephen
    Gelernter, Joel
    Covault, Jonathan
    Kallio, Antero
    Karhuvaara, Sakari
    Koivisto, Tiina
    Makela, Rauno
    Kranzler, Henry R.
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2008, 32 (07) : 1159 - 1166
  • [4] Single-nucleotide polymorphism in the human mu opioid receptor gene alters β-endorphin binding and activity:: Possible implications for opiate addiction
    Bond, C
    LaForge, KS
    Tian, MT
    Melia, D
    Zhang, SW
    Borg, L
    Gong, JH
    Schluger, J
    Strong, JA
    Leal, SM
    Tischfield, JA
    Kreek, MJ
    Yu, L
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (16) : 9608 - 9613
  • [5] Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females
    Clarke, T-K
    Crist, R. C.
    Ang, A.
    Ambrose-Lanci, L. M.
    Lohoff, F. W.
    Saxon, A. J.
    Ling, W.
    Hillhouse, M. P.
    Bruce, R. D.
    Woody, G.
    Berrettini, W. H.
    [J]. PHARMACOGENOMICS JOURNAL, 2014, 14 (03) : 303 - 308
  • [6] Low frequency genetic variants in the μ-opioid receptor (OPRM1) affect risk for addiction to heroin and cocaine
    Clarke, Toni-Kim
    Crist, Richard C.
    Kampman, Kyle M.
    Dackis, Charles A.
    Pettinati, Helen M.
    O'Brien, Charles P.
    Oslin, David W.
    Ferraro, Thomas N.
    Lohoff, Falk W.
    Berrettini, Wade H.
    [J]. NEUROSCIENCE LETTERS, 2013, 542 : 71 - 75
  • [7] OPRM1 A118G genotype fails to predict the effectiveness of naltrexone treatment for alcohol dependence
    Coller, Janet K.
    Cahill, Sharon
    Edmonds, Carolyn
    Farquharson, Aaron L.
    Longo, Marie
    Minniti, Rinaldo
    Sullivan, Thomas
    Somogyi, Andrew A.
    White, Jason M.
    [J]. PHARMACOGENETICS AND GENOMICS, 2011, 21 (12) : 902 - 905
  • [8] Association of dopamine and opioid receptor genetic polymorphisms with response to methadone maintenance treatment
    Crettol, Severine
    Besson, Jacques
    Croquette-Krokar, Marina
    Haemmig, Robert
    Gothuey, Isabelle
    Monnat, Martine
    Deglon, Jean-Jacques
    Preisig, Martin
    Eap, Chin B.
    [J]. PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY, 2008, 32 (07) : 1722 - 1727
  • [9] Case-control association analysis of polymorphisms in the delta-opioid receptor, OPRD1, with cocaine and opioid addicted populations
    Crist, R. C.
    Ambrose-Lanci, L. M.
    Vaswani, M.
    Clarke, T. K.
    Zeng, A.
    Yuan, C.
    Ferraro, T. N.
    Hakonarson, H.
    Kampman, K. M.
    Dackis, C. A.
    Pettinati, H. M.
    O'Brien, C. P.
    Oslin, D. W.
    Doyle, G. A.
    Lohoff, F. W.
    Berrettini, W. H.
    [J]. DRUG AND ALCOHOL DEPENDENCE, 2013, 127 (1-3) : 122 - 128
  • [10] Crist RC, 2014, PHARM BIOCH BEHAV, P123