实用医学杂志 ›› 2022, Vol. 38 ›› Issue (20): 2545-2548.doi: 10.3969/j.issn.1006⁃5725.2022.20.007

• 临床研究 • 上一篇    下一篇

阿尔茨海默病与microRNA⁃206基因多态性的关系

李俊彦1 余梦擎2 杨琳琳1 蔡钰莹1 李友3 杨宇1   

  1. 广东医科大学附属医院1 老年医学科,2 急诊医学中心,3 神经病学研究所(广东湛江 524000)

  • 出版日期:2022-10-25 发布日期:2022-10-25
  • 通讯作者: 杨宇 E⁃mail:canglu2008@163.com
  • 基金资助:
    国家自然科学基金项目(编号:81571157)

Association between microRNA⁃206 gene polymorphisms and Alzheimer′s disease

LI Junyan*YU Mengq⁃ ingYANG LinlinCAI YuyingLI YouYANG Yu.   

  1. Department of Geriatric MedicineAffiliated Hospital of Guang⁃ dong Medical UniversityZhanjiang 524000China

  • Online:2022-10-25 Published:2022-10-25
  • Contact: YANG Yu E⁃mail:canglu2008@163.com

摘要:

目的 分析阿尔茨海默病与 microRNA⁃206 基因多态性的关系。方法 采用 SNaPshot 技术对 100 例阿尔茨海默病患者(病例组)和 100 例健康体检者(对照组)的 microRNA⁃206 基因 rs16882131位点进行基因型检测,采用荧光定量多重聚合酶链反应方法检测两组外周血 microRNA⁃206 表达水平,并分析其与 rs16882131 位点不同基因型的关系。结果 病例组 rs16882131 位点的基因型和等位基因频率分布与对照组比较,差异均有统计学意义(基因型 CC vs. CT vs. TT:P = 0.027,TT + CT vs. CC:P = 0.034,OR =1.831;等位基因 T vs. C:P = 0.005,OR = 1.860);病例组外周血 microRNA⁃206 表达水平明显高于对照组(P < 0.05);对照组 TT + CT 基因型(T 等位基因携带)的 microRNA⁃206 表达水平明显高于 CC 基因型(P <0.05)。结论 microRNA⁃206 基因 rs16882131 位点多态性与阿尔茨海默病易感性有关,T 等位基因可能是阿尔茨海默病发病的危险因素。

关键词: microRNA?206, 阿尔茨海默病, 基因多态性

Abstract:

Objective To analyze the relationship of microRNA⁃206 gene polymorphisms and Alzheimer′s diseaseAD. Methods The SNP rs16882131 in the microRNA⁃206 was genotyped in 100 AD patients and 100 healthy controls using the SNaPshot technique. Quantitative real⁃time PCR was employed to evaluate the levels of microRNA ⁃206 expression in the peripheral blood of the two groupsand the association of the SNP rs16882131 with microRNA ⁃206 expression was further analyzed. Results There were significant differences in the genotype and allele frequencies of the SNP rs16882131 between the AD patients and controlsgenotype CC vs. CT vs. TTP = 0.027TT + CT vs. CCP = 0.034OR = 1.831allele T vs. CP = 0.005OR = 1.860. The microRNA⁃ 206 expression in the peripheral blood of the AD patients was significantly higher than that in the healthy controls P < 0.05. Additionallythe microRNA ⁃206 expression in the healthy controls who were TT + CT genotypes of the SNP rs16882131 was significantly higher compared with the CC genotypesP < 0.05. Conclusion The SNP rs16882131 in the microRNA⁃206 is associated with the susceptibility to the ADand the T allele may contribute to risk roles in the AD.

Key words:

microRNA?206, Alzheimer′s disease, gene polymorphisms