Xu Ran, Liu Xin, Zhou Fan, Liu Jie, Bai Dunyao
College of Nursing, Chengdu University of Traditional Chinese Medicine No. 1166, Liutai Avenue, Wenjiang District, Chengdu 611137, Sichuan, China.
Department of Orthopedics, Second Affiliated Hospital of The Army Medical University (Xinqiao Hospital) No. 83 Xinqiao Main Street, Shapingba District, Chongqing 400037, China.
Am J Transl Res. 2025 Jul 25;17(7):5654-5666. doi: 10.62347/SUPA1847. eCollection 2025.
We conducted a systematic review and meta-analysis to clarify the relationship between these gene polymorphisms and Osteoarthritis (OA) risk. We searched electronic databases and found 736 related reports, five of which were ultimately included in the study. The articles ranged from 2014 to 2019 and included both Asian and Caucasian populations. Genotypes were categorized into TT, TC, and CC across case and control groups. The meta-analysis of interleukin-17A (IL-17A; rs2275913) showed no significant correlation with OA in the overall human population's allele model, codominance model, dominance model, and recessive model (P=0.97, 0.94, 0.77, 0.80, 0.85). Ethnic subgroup analysis showed no association between the Asian or Caucasian populations' IL-17A gene and OA. However, the meta-analysis of interleukin-17F (IL-17F; rs763780) showed that this gene is related to OA in the overall population and each single nucleotide polymorphism (SNP) genetic model (-values: 0.0001, 0.0003, 0.01, 0.01, 0.0008). Ethnic subgroup analysis revealed that the IL-17F gene in the Asian population is related to OA, but only the allele and dominant models of the IL-17F gene in the Caucasian population were related to OA. The IL-17F polymorphism appears to be a risk factor for OA, with Asian populations more susceptible than Caucasians. The IL-17A showed no association with OA.
我们进行了一项系统评价和荟萃分析,以阐明这些基因多态性与骨关节炎(OA)风险之间的关系。我们检索了电子数据库,共找到736篇相关报告,最终纳入研究的有5篇。这些文章发表于2014年至2019年,涵盖亚洲和白种人群体。病例组和对照组的基因型分为TT、TC和CC。白细胞介素-17A(IL-17A;rs2275913)的荟萃分析显示,在总体人群的等位基因模型、共显性模型、显性模型和隐性模型中,与OA均无显著相关性(P = 0.97、0.94、0.77、0.80、0.85)。种族亚组分析表明,亚洲或白种人群体的IL-17A基因与OA均无关联。然而,白细胞介素-17F(IL-17F;rs763780)的荟萃分析显示,该基因在总体人群及各单核苷酸多态性(SNP)遗传模型中均与OA相关(P值分别为0.0001、0.0003、0.01、0.01、0.0008)。种族亚组分析显示,亚洲人群体的IL-17F基因与OA相关,但白种人群体中只有IL-17F基因的等位基因和显性模型与OA相关。IL-17F多态性似乎是OA的一个风险因素,亚洲人群比白种人更易患病。IL-17A与OA无关联。
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