Fan Leijun, Wu Ru, Sun Yunyun, Li Xia, Chen Liang, Zhang Jun, Miao Chenghao
Department of Anesthesia, First People's Hospital of Linping District of Hangzhou City, 369 Yingbin Road, Linping District, Hangzhou 311100, China.
Department of Anesthesia, Shanghai Geriatrics Medical Center, 2560 Chunshen Road, Minhang District, Shanghai 201104, China.
Toxicol Res (Camb). 2025 Jan 21;14(1):tfae227. doi: 10.1093/toxres/tfae227. eCollection 2025 Feb.
The latest studies have demonstrated that aberrant expression of microRNA-146a is related to cognitive decline. The rs57095329 polymorphism occurring in the miR-146a promoter modulates its expression and causes downstream pathogenicity. A case-control study in a Chinese Han population was established to investigate the genetic association between the miR-146a rs57095329 polymorphism and postoperative cognitive dysfunction (POCD). 242 patients with POCD and another 238 non-POCD cases were enrolled in the case-control study. Serum miR-146a levels were detected by qRT-PCR. miR-146a rs57095329 polymorphism was genotyped using the ABI PRISM SNaPshot method. The genetic association between the rs57095329 polymorphism and POCD was assessed by regression analysis. No significant difference was detected for age, gender and BMI between POCD and non-POCD groups. MiR-146a rs57095329 polymorphism revealed significant generic associations with POCD in both dominant and recessive models, and the AA genotype may increase the risk of developing POCD. qRT-PCR indicated the upregulation of miR-146a level in POCD group. Serum levels of miR-146a and inflammatory factors were higher in rs57095329 AA genotype carriers than in AG/GG genotype carriers. Rs57095329 polymorphism was independently associated with the development of POCD. In conclusion, miR-146a rs57095329 polymorphism was associated with POCD in the Chinese Han population. The rs57095329 AA genotype was the causative genotype for POCD and was related to the upregulation of miR-146a and inflammatory factor levels.
最新研究表明,微小RNA-146a(miR-146a)的异常表达与认知功能衰退有关。miR-146a启动子中发生的rs57095329多态性调节其表达并导致下游致病性。在中国汉族人群中开展了一项病例对照研究,以调查miR-146a rs57095329多态性与术后认知功能障碍(POCD)之间的遗传关联。242例POCD患者和另外238例非POCD患者纳入了该病例对照研究。采用qRT-PCR检测血清miR-146a水平。使用ABI PRISM SNaPshot方法对miR-146a rs57095329多态性进行基因分型。通过回归分析评估rs57095329多态性与POCD之间的遗传关联。POCD组和非POCD组在年龄、性别和体重指数方面未检测到显著差异。miR-146a rs57095329多态性在显性和隐性模型中均显示与POCD存在显著的遗传关联,AA基因型可能增加患POCD的风险。qRT-PCR表明POCD组中miR-146a水平上调。rs57095329 AA基因型携带者的血清miR-146a水平和炎症因子水平高于AG/GG基因型携带者。rs57095329多态性与POCD的发生独立相关。总之,miR-146a rs57095329多态性与中国汉族人群的POCD有关。rs57095329 AA基因型是POCD的致病基因型,并且与miR-146a和炎症因子水平上调有关。