Strauss J, Barr C L, George C J, King N, Shaikh S, Devlin B, Kovacs M, Kennedy J L
Centre for Addiction and Mental Health, University of Toronto, 250 College Str., Toronto, Ontario, Canada.
Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):16-9. doi: 10.1002/ajmg.b.30041.
Brain-derived neurotrophic factor (BDNF) is a nerve growth factor that has antidepressant-like effects in animals. BDNF gene polymorphisms have been associated with bipolar disorder. We tested two genetic polymorphisms of BDNF for their association with childhood-onset mood disorders (COMD) within the context of a case-control design. Two BDNF polymorphisms, a dinucleotide repeat (GT)(n), and a single nucleotide polymorphism (SNP) in the coding region, val66met, were genotyped in 99 adults with a history of COMD and matched psychiatrically healthy controls. A genomic control (GC) method was used to evaluate population substructure. Alleles at (GT)(n) were highly associated with COMD in this sample (chi(2) = 17.8; d.f. = 5; P = 0.0032). The odds of carrying the 168 bp allele were 3.94 times greater for cases than controls (CI = 1.72-9.04). Alleles of val66met were not significantly associated with COMD. GC analysis suggested population substructure was not a confounder of association. Analysis of haplotypes, in which (GT)(n) was treated as a binary variable (long vs. short alleles), provided significant evidence that the haplotype val/short contributes to liability to COMD. The BDNF (GT)(n) marker and the val/short haplotype are associated with COMD in this sample, in accordance with the previously described neurotrophic hypothesis of depression and some previous studies of association for bipolar disorder and neuroticism.
脑源性神经营养因子(BDNF)是一种在动物中具有类抗抑郁作用的神经生长因子。BDNF基因多态性与双相情感障碍有关。我们在病例对照设计的背景下,测试了BDNF的两种基因多态性与儿童期起病的情绪障碍(COMD)的关联。对99名有COMD病史的成年人及与之匹配的精神健康对照者,进行了BDNF的两种多态性基因分型,一种是二核苷酸重复序列(GT)(n),另一种是编码区的单核苷酸多态性(SNP),即val66met。采用基因组对照(GC)方法评估群体亚结构。在该样本中,(GT)(n)的等位基因与COMD高度相关(χ² = 17.8;自由度 = 5;P = 0.0032)。病例携带168 bp等位基因的几率是对照的3.94倍(可信区间 = 1.72 - 9.04)。val66met的等位基因与COMD无显著关联。GC分析表明群体亚结构不是关联的混杂因素。单倍型分析中,将(GT)(n)视为二元变量(长等位基因与短等位基因),提供了重要证据表明单倍型val/短增加了COMD的易感性。在该样本中,BDNF(GT)(n)标记和val/短单倍型与COMD相关,这与先前描述的抑郁症神经营养假说以及一些先前关于双相情感障碍和神经质的关联研究一致。