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日本脑源性神经营养因子基因多态性与甲基苯丙胺滥用者之间的关联研究。

Association study between brain-derived neurotrophic factor gene polymorphisms and methamphetamine abusers in Japan.

作者信息

Itoh Kanako, Hashimoto Kenji, Shimizu Eiji, Sekine Yoshimoto, Ozaki Norio, Inada Toshiya, Harano Mutsuo, Iwata Nakao, Komiyama Tokutaro, Yamada Mitsuhiko, Sora Ichiro, Nakata Kenji, Ujike Hiroshi, Iyo Masaomi

机构信息

Department of Psychiatry, Chiba University Graduate School of Medicine, 1-8-1 Inohana, Chiba 260-8670, Japan.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):70-3. doi: 10.1002/ajmg.b.30097.

Abstract

Several lines of evidence suggest that genetic factors might contribute to drug abuse vulnerability. Recent genomic scans for association demonstrated that the brain-derived neurotrophic factor (BDNF) gene was associated with drug abuse vulnerability. In this study, we analyzed association of two BDNF gene single nucleotide polymorphisms (SNPs), 132C > T (C270T named formerly) in the noncoding region of exon V and 196G > A (val66met) in the coding region of exon XIIIA, with methamphetamine (MAP) abuse in Japan. No significant differences were found in the frequency of the genotype or allele in these two SNPs between MAP abusers and controls (132C > T in exon V: genotype, P = 0.586, allele, P = 0.594; 196G > A (val66met) in exon XIIIA: genotype, P = 0.889, allele, P = 0.713). Furthermore, there was no difference between clinical parameters (e.g., prognosis psychosis, spontaneous relapse, or poly-substance abuse) and the two SNPs of BDNF gene. These results suggest that the two SNPs (132C > T in exon V and 196G > A (val66met) in exon XIIIA) of the BDNF gene may not be associated with Japanese MAP abusers. This article contains supplementary material, which may be viewed at the American Journal of Medical Genetics website at http://www.interscience.wiley.com/jpages/0148-7299:1/suppmat/index.html.

摘要

多项证据表明,遗传因素可能导致药物滥用易感性。最近的全基因组关联扫描显示,脑源性神经营养因子(BDNF)基因与药物滥用易感性有关。在本研究中,我们分析了BDNF基因的两个单核苷酸多态性(SNP),即外显子V非编码区的132C>T(以前称为C270T)和外显子XIIIA编码区的196G>A(val66met)与日本甲基苯丙胺(MAP)滥用之间的关联。在MAP滥用者和对照组之间,这两个SNP的基因型或等位基因频率没有显著差异(外显子V中的132C>T:基因型,P=0.586,等位基因,P=0.594;外显子XIIIA中的196G>A(val66met):基因型,P=0.889,等位基因,P=0.713)。此外,临床参数(如预后性精神病、自发复发或多物质滥用)与BDNF基因的两个SNP之间也没有差异。这些结果表明,BDNF基因的两个SNP(外显子V中的132C>T和外显子XIIIA中的196G>A(val66met))可能与日本MAP滥用者无关。本文包含补充材料,可在美国医学遗传学杂志网站http://www.interscience.wiley.com/jpages/0148-7299:1/suppmat/index.html上查看。

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