Genome-wide association for methamphetamine dependence: convergent results from 2 samples.

نویسندگان

  • George R Uhl
  • Tomas Drgon
  • Qing-Rong Liu
  • Catherine Johnson
  • Donna Walther
  • Tokutaro Komiyama
  • Mutsuo Harano
  • Yoshimoto Sekine
  • Toshiya Inada
  • Norio Ozaki
  • Masaomi Iyo
  • Nakao Iwata
  • Mitsuhiko Yamada
  • Ichiro Sora
  • Chih-Ken Chen
  • Hsing-Cheng Liu
  • Hiroshi Ujike
  • Shih-Ku Lin
چکیده

CONTEXT We can improve understanding of human methamphetamine dependence, and possibly our abilities to prevent and treat this devastating disorder, by identifying genes whose allelic variants predispose to methamphetamine dependence. OBJECTIVE To find "methamphetamine dependence" genes identified by each of 2 genome-wide association (GWA) studies of independent samples of methamphetamine-dependent individuals and matched controls. DESIGN Replicated GWA results in each of 2 case-control studies. SETTING Japan and Taiwan. PARTICIPANTS Individuals with methamphetamine dependence and matched control subjects free from psychiatric, substance abuse, or substance dependence diagnoses (N = 580). MAIN OUTCOME MEASURES "Methamphetamine dependence" genes that were reproducibly identified by clusters of nominally positive single-nucleotide polymorphisms (SNPs) in both samples in ways that were unlikely to represent chance observations, based on Monte Carlo simulations that corrected for multiple comparisons, and subsets of "methamphetamine dependence" genes that were also identified by GWA studies of dependence on other addictive substances, success in quitting smoking, and memory. RESULTS Genes identified by clustered nominally positive SNPs from both samples were unlikely to represent chance observations (Monte Carlo P < .00001). Variants in these "methamphetamine dependence" genes are likely to alter cell adhesion, enzymatic functions, transcription, cell structure, and DNA, RNA, and/or protein handling or modification. Cell adhesion genes CSMD1 and CDH13 displayed the largest numbers of clustered nominally positive SNPs. "Methamphetamine dependence" genes overlapped, to extents much greater than chance, with genes identified in GWA studies of dependence on other addictive substances, success in quitting smoking, and memory (Monte Carlo P range < .04 to < .00001). CONCLUSION These data support polygenic contributions to methamphetamine dependence from genes that include those whose variants contribute to dependence on several addictive substances, success in quitting smoking, and mnemonic processes.

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عنوان ژورنال:
  • Archives of general psychiatry

دوره 65 3  شماره 

صفحات  -

تاریخ انتشار 2008