摘要
目的探讨辽宁地区散发性阿尔茨海默病(AD)与HLA相关位点基因遗传多态性的关联性。方法采用特异性寡核苷酸序列探针分析法(SSO)检测辽宁地区44名散发性阿尔茨海默病患者(实验组)和90名健康老人(对照组)HLA-A、HLA-B和HLA-DRB1位点基因遗传多态性。应用Arlequin3.5软件进行Hardy-Weinberg平衡、单体型频率的分析;应用SPSS17.0软件进行卡方检验,比较2组间等位基因和单体型频率的差异。结果实验组和对照组HLA-A、B、DRB1位点的各个等位基因频率的差异均不具统计学意义(P〉0.05);HLA-A-B单体型频率最高的为A* 30-B* 13、A* 02-B* 46、A* 02-B* 15,2组间高频单体型频率的差异也不具统计学意义(P〉0.05)。结论辽宁地区散发性阿尔茨海默病与HLA-A、HLA-B和HLA-DRB1位点基因遗传多态性无相关性。
Objective To explore the connections between gene polymorphism of HLA and Alzheimer's disease. Methods A total of 44 Liaoning Han patients with Alzheimer's disease and 90 unrelated healthy controls were recruited in this study. SSO method was used to detect the genotypes of HLA-A,HLA-B and HLA-DRB1. Hardy-Weinberg equilibrium were evaluated by chi-square tests. Hardy-Weinberg equilibrium and haplotype frequencies were carried out using Arlequin3. 5 software. Differences in allelic and haplotype frequencies were evaluated by chi-square test using SPSS 17. 0 statistical software. Results No significant differences in all alleles of HLA-A,HLA-B and HLA-DRB1 between the two groups(P〈0. 05). High frequent haplotypes were A* 30-B* 13,A* 02-B* 46,A* 33-B* 58,no significant differences in these haplotypes between the two groups either(P〉0. 05). Conclusion Gene polymorphisms of HLA-A,HLA-B and HLA-DRB1 are not likely to be associated with risk of AD in Liaoning Han population.
作者
范亚欣
邵林楠
宋文倩
周世航
FAN Yaxin, SHAO Linnan, SONG Wenqian, ZHOU Shihang.(Dalian Blood Center, Dalian 116001, Liaoning, China)
出处
《中国输血杂志》
CAS
2018年第1期41-43,共3页
Chinese Journal of Blood Transfusion