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白细胞介素-6和基质金属蛋白酶-3基因多态性与青少年特发性脊柱侧凸的关联:一项系统评价和荟萃分析

Association of IL‑6 and MMP‑3 gene polymorphisms with adolescent idiopathic scoliosis: A systematic review and meta‑analysis.

作者信息

Wang Yue-Peng, Qin Shi-Lei, Yang Su, Xu Yun-Feng, Han Peng-Fei, Liu Ai-Hua, Hou Ke-Dong, He Jian-Ping

机构信息

Department of Orthopaedics, Beijing Friendship Hospital Pinggu Campus, Capital Medical University, Beijing 101200, P.R. China.

Department of Orthopaedics, Changzhi Yunfeng Hospital, Changzhi, Shanxi 046000, P.R. China.

出版信息

Exp Ther Med. 2024 Apr 26;27(6):267. doi: 10.3892/etm.2024.12555. eCollection 2024 Jun.

DOI:10.3892/etm.2024.12555
PMID:38756907
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11097290/
Abstract

The pathogenesis of adolescent idiopathic scoliosis (AIS) remains unclear. It has been found that interleukin-6 (IL-6) rs1800795 locus and matrix metalloproteinase-3 (MMP-3) rs3025058 locus gene polymorphisms may be associated with AIS susceptibility, which has been controversial and needs to be further confirmed by updated meta-analysis. The aim of the present study was to investigate the association of MMP-3 rs3025058 and IL-6 rs1800795 single nucleotide polymorphisms (SNPs) with susceptibility to AIS. All relevant articles that met the criteria were retrieved and included, and the publication dates were limited from January 2005 to December 2023. The allele frequencies and different genotype frequencies of IL-6 rs1800795 and MMP-3 rs3025058 loci in each study were extracted and statistically analyzed by ReviewManager 5.4 software, and the odds ratio (OR) and 95% confidence interval (95% CI) of different genetic models were calculated. The results of the meta-analysis showed that there was no significant association between the gene polymorphism of IL-6 rs1800795 locus and the pathogenesis of AIS. The allele 5A and genotype 5A5A of MMP-3 rs3025058 SNP were associated with AIS susceptibility (5A vs. 6A, OR=1.18; 95% CI, 1.04-1.33; 5A5A vs. 6A6A, OR=1.65; 95% CI, 1.23-2.21; and 5A5A vs. 5A6A + 6A6A, OR=1.54; 95% CI, 1.19-1.99). Results of subgroup analysis revealed that the allele 5A and genotype 5A5A of MMP-3 rs3025058 SNP were associated with AIS susceptibility in the Caucasian population, and the susceptibility of AIS was associated with the genotype 5A5A of MMP-3 rs3025058 SNP in an Asian population. There was no significant association between the gene polymorphism of IL-6 rs1800795 locus and the pathogenesis of AIS, while the allele 5A of MMP-3 rs3025058 locus was associated with the susceptibility to AIS, especially in the Caucasian population.

摘要

青少年特发性脊柱侧凸(AIS)的发病机制尚不清楚。已发现白细胞介素-6(IL-6)rs1800795位点和基质金属蛋白酶-3(MMP-3)rs3025058位点基因多态性可能与AIS易感性相关,这一观点一直存在争议,需要通过更新的荟萃分析进一步证实。本研究的目的是探讨MMP-3 rs3025058和IL-6 rs1800795单核苷酸多态性(SNP)与AIS易感性的关系。检索并纳入了所有符合标准的相关文章,发表日期限制在2005年1月至2023年12月。提取每项研究中IL-6 rs1800795和MMP-3 rs3025058位点的等位基因频率和不同基因型频率,并用ReviewManager 5.4软件进行统计分析,计算不同遗传模型的比值比(OR)和95%置信区间(95%CI)。荟萃分析结果显示,IL-6 rs1800795位点基因多态性与AIS发病机制之间无显著关联。MMP-3 rs3025058 SNP的5A等位基因和5A5A基因型与AIS易感性相关(5A vs. 6A,OR=1.18;95%CI,1.04-1.33;5A5A vs. 6A6A,OR=1.65;95%CI,1.23-2.21;5A5A vs. 5A6A + 6A6A,OR=1.54;95%CI,1.19-1.99)。亚组分析结果显示,MMP-3 rs3025058 SNP的5A等位基因和5A5A基因型在白种人群中与AIS易感性相关,在亚洲人群中AIS易感性与MMP-3 rs3025058 SNP的5A5A基因型相关。IL-6 rs1800795位点基因多态性与AIS发病机制之间无显著关联,而MMP-3 rs3025058位点的5A等位基因与AIS易感性相关,尤其是在白种人群中。

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