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Gender-specific contribution of the GABAA subunit genes on 5q33 in methamphetamine use disorder

  • S. K. Lin
  • , C. K. Chen
  • , D. Ball
  • , H. C. Liu
  • , E. W. Loh*
  • *Corresponding author for this work
  • Taipei City Hospital
  • Taipei Medical University
  • Chang Gung Memorial Hospital
  • King's College London
  • Academia Sinica Taiwan HQ

Research output: Contribution to journalJournal Article peer-review

43 Scopus citations

Abstract

Family and twins studies have suggested that genetic factors are involved in the development of substance use disorders. Several unrelated case/control association studies have reported associations of the GABAA subunit genes on 5q33 with the development of alcohol dependence. We hypothesized that these particular GABAA subunit genes also contribute to the development of methamphetamine use disorder. To test our hypothesis, we recruited cases using a series of questionnaires. Among the polymorphic SNPs, significant differences between cases and controls were identified in the female sample in the rs2279020 of the GABAAα1 subunit gene, and the novel SNP rs4480617 in the GABA2 subunit gene. No associations were found in the male sample. Further haplotype analysis identified several marker blocks significantly associated with methamphetamine use disorder in females; each block consists of the rs4480617. Our study provides preliminary evidence that the GABAA subunit genes on 5q33 may preferentially contribute to methamphetamine use disorder in females.

Original languageEnglish
Pages (from-to)349-355
Number of pages7
JournalPharmacogenomics Journal
Volume3
Issue number6
DOIs
StatePublished - 2003

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Alcohol dependence
  • Alcoholism
  • Amphetamine
  • Haplotype
  • Polymorphism
  • Substance use disorder

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