系统性红斑狼疮患者miR-21基因多态性与认知功能的关联

Personalized medicine Pub Date : 2025-04-01 Epub Date: 2025-03-14 DOI:10.1080/17410541.2025.2478809
Tiantian Wei, Jing Shen, Lijun He, Wei Zhou, Hui Zhang
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引用次数: 0

摘要

目的:miR-21的遗传变异rs13137与许多疾病的易感性相关。然而,中国系统性红斑狼疮(SLE)患者与认知功能障碍(CD)的关系尚不清楚。材料与方法:招募230例SLE患者(非CD)和230例SLE相关CD患者(CD)。采用qRT-PCR计算MiR-21水平。建立ROC曲线评价诊断性。多因素logistic回归分析确定独立危险因素。结果:CD组miR-21水平明显升高。与AA携带者相比,CD组rs13137 AT/TT携带者miR-21水平显著低于非CD组。AUC为0.9023,敏感性78.70%,特异性90.87%。基因型和等位基因频率的比较表明,携带rs13137 AT/TT基因型的SLE患者发生CD的风险较低。多因素logistic回归分析显示,rs13137多态性、受教育年限、MoCA评分与CD风险相关。结论:miR-21 rs13137多态性与中国人群的CD风险相关。MiR-21在rs13137 AT/TT携带者中显著低于AA基因型,AT/TT基因型与SLE患者低CD风险相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Association of miR-21 gene polymorphisms with cognitive function in patients with systemic lupus erythematosus.

Objectives: The genetic variant rs13137 of miR-21 is associated with susceptibility in many diseases. However, the association with cognitive dysfunction (CD) in Chinese patients with systemic lupus erythematosus (SLE) remains unclear.

Materials and methods: Two hundred and thirty SLE patients (Non-CD) and 230 SLE-related CD patients (CD) were recruited. MiR-21 level was calculated by qRT-PCR. The ROC curve was established to evaluate the diagnosibility. The independent risk factors were identified by multivariate logistic regression analysis.

Results: The miR-21 in CD group was obviously increased. Compared to AA carriers, the miR-21 level in carriers of rs13137 AT/TT in CD group were significantly lower than those in Non-CD group. The AUC was 0.9023 with sensitivity of 78.70% and specificity of 90.87%. Comparison of genotype and allele frequencies indicated that SLE patients carrying rs13137 AT/TT genotype had low risk of CD. Multivariate logistic regression analysis showed that the rs13137 polymorphism, education years, and MoCA score were correlated with CD risk.

Conclusion: The miR-21 rs13137 polymorphism was correlated with CD risk in the Chinese population. MiR-21 in rs13137 AT/TT carriers was significantly lower than that of AA genotype and the AT/TT genotype was correlated with low CD risk in SLE patients.

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