Vepsäläinen Saila, Castren Eero, Helisalmi Seppo, Iivonen Susan, Mannermaa Arto, Lehtovirta Maarit, Hänninen Tuomo, Soininen Hilkka, Hiltunen Mikko
Dept. of Neuroscience and Neurology, Kuopio University and University Hospital, 1627, 70211 Kuopio, Finland.
J Neurol. 2005 Apr;252(4):423-8. doi: 10.1007/s00415-005-0667-5. Epub 2005 Feb 23.
According to previous biochemical and genetic findings, brain-derived neurotrophic factor (BDNF), via activation of its tyrosine kinase receptor B (TrkB), is considered as a plausible candidate for contributing to Alzheimer's disease (AD). To examine the genetic association of BDNF and TrkB genes with AD, we genotyped multiple single nucleotide polymorphisms (SNPs) within these genes among 375 Finnish AD patients and 460 control subjects. Single locus and multi-loci haplotype association analyses of BDNF and TrkB gene SNPs did not reveal significant differences between unstratified AD and control groups. In the case of BDNF SNPs, different allele and haplotype frequencies were observed when 160 sporadic AD cases were compared with 460 control subjects. However, these differences did not remain statistically significant after multiple corrections. We conclude that BDNF and TrkB genes are not contributing significant risk effect among Finnish AD patients.
根据先前的生化和遗传学研究结果,脑源性神经营养因子(BDNF)通过激活其酪氨酸激酶受体B(TrkB),被认为是导致阿尔茨海默病(AD)的一个可能候选因素。为了研究BDNF和TrkB基因与AD的遗传关联,我们对375名芬兰AD患者和460名对照受试者的这些基因中的多个单核苷酸多态性(SNP)进行了基因分型。BDNF和TrkB基因SNP的单基因座和多基因座单倍型关联分析未发现未分层的AD组和对照组之间存在显著差异。对于BDNF SNP,当将160例散发性AD病例与460名对照受试者进行比较时,观察到了不同的等位基因和单倍型频率。然而,经过多次校正后,这些差异在统计学上不再显著。我们得出结论,BDNF和TrkB基因在芬兰AD患者中没有显著的风险作用。