University of Szeged, Department of Psychiatry, Szeged, Hungary.
Neurosci Lett. 2013 Feb 8;534:233-6. doi: 10.1016/j.neulet.2012.12.020. Epub 2012 Dec 27.
Genetic variants of the serotonergic neurotransmitter system are potential contributing factors in the pathological processes underlying Alzheimer's disease (AD). We examined polymorphisms of the serotonin transporter (SLC6A4) and serotonin receptor 2A (HTR2A) genes for possible association with AD, and therefore genotyped 5-HTTLPR, STin2-VNTR and HTR2A T102C polymorphisms in 252 Hungarian AD patients and 234 ethnically matched control individuals. We did not detect statistically significant differences in genotype distribution comparing the AD and the control group when the polymorphisms were investigated separately. Logistic regression analyses, however, revealed an interaction effect between 5-HTTLPR and HTR2A T102C (p=0.019), but not between 5-HTTLPR and STin2-VNTR (p=0.494) or STin2-VNTR and HTR2A T102C (p=0.310) polymorphisms. Our study suggests no individual influence of the investigated polymorphisms but a potential combined effect of the 5-HTTLPR L/L and HTR2A T102C C/C genotypes on AD risk. However, the results need to be treated with considerable caution, and further analyses in larger samples are required.
血清素能神经递质系统的遗传变异是阿尔茨海默病(AD)病理过程的潜在影响因素。我们研究了 5-羟色胺转运体(SLC6A4)和 5-羟色胺受体 2A(HTR2A)基因的多态性与 AD 的可能相关性,并因此对 252 名匈牙利 AD 患者和 234 名种族匹配的对照组个体的 5-HTTLPR、STin2-VNTR 和 HTR2A T102C 多态性进行了基因分型。当单独研究这些多态性时,我们没有发现 AD 组和对照组在基因型分布上存在统计学上的显著差异。然而,逻辑回归分析显示 5-HTTLPR 和 HTR2A T102C 之间存在交互作用(p=0.019),但 5-HTTLPR 和 STin2-VNTR 之间(p=0.494)或 STin2-VNTR 和 HTR2A T102C 之间(p=0.310)没有这种作用。我们的研究表明,所研究的多态性没有个体影响,但 5-HTTLPR L/L 和 HTR2A T102C C/C 基因型的潜在组合可能对 AD 风险有影响。然而,结果需要谨慎对待,需要在更大的样本中进行进一步分析。