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Review
. 2010 Feb:1187:184-207.
doi: 10.1111/j.1749-6632.2009.05275.x.

Search for genetic markers and functional variants involved in the development of opiate and cocaine addiction and treatment

Affiliations
Review

Search for genetic markers and functional variants involved in the development of opiate and cocaine addiction and treatment

Vadim Yuferov et al. Ann N Y Acad Sci. 2010 Feb.

Abstract

Addiction to opiates and illicit use of psychostimulants is a chronic, relapsing brain disease that, if left untreated, can cause major medical, social, and economic problems. This article reviews recent progress in studies of association of gene variants with vulnerability to develop opiate and cocaine addictions, focusing primarily on genes of the opioid and monoaminergic systems. In addition, we provide the first evidence of a cis-acting polymorphism and a functional haplotype in the PDYN gene, of significantly higher DNA methylation rate of the OPRM1 gene in the lymphocytes of heroin addicts, and significant differences in genotype frequencies of three single-nucleotide polymorphisms of the P-glycoprotein gene (ABCB1) between "higher" and "lower" methadone doses in methadone-maintained patients. In genomewide and multigene association studies, we found association of several new genes and new variants of known genes with heroin addiction. Finally, we describe the development and application of a novel technique: molecular haplotyping for studies in genetics of drug addiction.

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Conflict of interest statement

Conflicts of interest: The authors declare no conflicts of interest.

References

    1. Kreek MJ, et al. Pharmacogenetics and human molecular genetics of opiate and cocaine addictions and their treatments. Pharmacol. Rev. 2005;57:1–26. - PubMed
    1. Savage SR, et al. Challenges in using opioids to treat pain in persons with substance use disorders. Addict. Sci. Clin. Pract. 2008;4:4–25. - PMC - PubMed
    1. Kreek MJ, LaForge KS. Stress responsivity, addiction, and a functional variant of the human mu-opioid receptor gene. Mol. Interv. 2007;7:74–78. - PubMed
    1. Kreek MJ, et al. Bidirectional translational research: Progress in understanding addictive diseases. Neuropharmacology. 2009;56(Suppl 1):32–43. - PMC - PubMed
    1. Bond C, et al. Single-nucleotide polymorphism in the human mu opioid receptor gene alters beta-endorphin binding and activity: possible implications for opiate addiction. Proc. Natl. Acad. Sci. U. S. A. 1998;95:9608–9613. - PMC - PubMed

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