Glutamate cysteine ligase modifier (GCLM) subunit gene is not associated with methamphetamine-use disorder or schizophrenia in the Japanese population

Ann N Y Acad Sci. 2008 Oct:1139:63-9. doi: 10.1196/annals.1432.022.

Abstract

A recent study showed a significant association between schizophrenia in European samples and the glutamate cysteine ligase modifier (GCLM) subunit gene, which is the key glutathione (GSH)-synthesizing enzyme. Since the symptoms of methamphetamine (METH)-induced psychosis are similar to those of schizophrenia, the GCLM gene is thought to be a good candidate gene for METH-use disorder or related disorders. To evaluate the association between the GCLM gene and METH-use disorder and schizophrenia, we conducted a case-control study of Japanese subjects (METH-use disorder, 185 cases; schizophrenia, 742 cases; and controls, 819). Four SNPs (2 SNPs from an original report and JSNP database, and 2 "tagging SNPs" from HapMap database) in the GCLM gene were examined in this association analysis; one SNP showed an association with both METH-use disorder and METH-induced psychosis. After Bonferroni's correction for multiple testing, however, this significance disappeared. No significant association was found with schizophrenia. Our findings suggest that a common genetic variation in the GCLM gene might not contribute to the risk of METH-use disorder and schizophrenia in the Japanese population.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Amphetamine-Related Disorders / genetics*
  • Asian People / genetics*
  • Female
  • Genotype
  • Glutamate-Cysteine Ligase / chemistry
  • Glutamate-Cysteine Ligase / genetics*
  • Humans
  • Linkage Disequilibrium
  • Male
  • Methamphetamine / pharmacology*
  • Middle Aged
  • Polymorphism, Single Nucleotide
  • Protein Subunits / genetics*
  • Psychoses, Substance-Induced / genetics*
  • Schizophrenia / genetics*

Substances

  • Protein Subunits
  • Methamphetamine
  • Glutamate-Cysteine Ligase