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白细胞介素-6与基质金属蛋白酶-3基因多态性和青少年特发性脊柱侧凸之间的关联:一项病例对照研究。

Association between IL-6 and MMP-3 gene polymorphisms and adolescent idiopathic scoliosis: a case-control study.

作者信息

Aulisa Lorenzo, Papaleo Pierangelo, Pola Enrico, Angelini Flavia, Aulisa Angelo G, Tamburrelli Francesco C, Pola Paolo, Logroscino Carlo A

机构信息

A. Gemelli University Hospital, 8, Rome, Italy.

出版信息

Spine (Phila Pa 1976). 2007 Nov 15;32(24):2700-2. doi: 10.1097/BRS.0b013e31815a5943.

Abstract

STUDY DESIGN

Case-control study.

OBJECTIVE

As inflammation plays a key role in the etiology of intervertebral disc degeneration, we suggest a possible contribution of pro-inflammatory gene polymorphisms in the pathogenesis of adolescent idiopathic scoliosis (AIS).

SUMMARY OF BACKGROUND DATA

The nucleus pulposus of scoliotic discs responds to exogenous stimuli by secreting interleukin-6 (IL-6) and other inflammatory cytokines. The association between matrix metalloproteinases (MMPs) and disc degeneration has been reported by several investigators. A human MMP-3 promoter 5A/6A gene polymorphism regulates MMP-3 genes expression, while the G/C polymorphism of the promoter region of IL-6 gene influences levels and functional activity of the IL-6 protein.

METHODS

We conducted a case-control study to investigate whether the 5A/6A polymorphism of the MMP-3 gene and the G/C polymorphism of the promoter region of IL-6 gene were associated with susceptibility to AIS.

RESULTS

The frequency of the 5A/5A genotype of MMP-3 gene polymorphism in patients with scoliosis was almost 3 times higher than in controls (30.2% vs. 11.2%, p 0.001), and the frequency of the G/G genotype of IL-6 gene polymorphism in patients with scoliosis was almost 2 times higher than in controls (52.8% vs. 26.2%, P < 0.001). 5A/5A genotype of MMP-3 gene polymorphism and G/G genotype of IL-6 gene polymorphism are independently associated with a higher risk of scoliosis (odds ratio, respectively, 3.34 and 10.54).

CONCLUSION

This is the first study that has evaluated the possibility that gene variants of IL-6 and MMPs might be associated with scoliosis and suggests that MMP-3 and IL-6 promoter polymorphisms constitute important factors for the genetic predisposition to scoliosis.

摘要

研究设计

病例对照研究。

目的

由于炎症在椎间盘退变的病因学中起关键作用,我们推测促炎基因多态性可能在青少年特发性脊柱侧凸(AIS)的发病机制中发挥作用。

背景数据总结

脊柱侧凸椎间盘的髓核通过分泌白细胞介素-6(IL-6)和其他炎性细胞因子对外源性刺激作出反应。几位研究者报道了基质金属蛋白酶(MMPs)与椎间盘退变之间的关联。人类MMP-3启动子5A/6A基因多态性调节MMP-3基因表达,而IL-6基因启动子区域的G/C多态性影响IL-6蛋白的水平和功能活性。

方法

我们进行了一项病例对照研究,以调查MMP-3基因的5A/6A多态性和IL-6基因启动子区域的G/C多态性是否与AIS易感性相关。

结果

脊柱侧凸患者中MMP-3基因多态性的5A/5A基因型频率几乎是对照组的3倍(30.2%对11.2%,p<0.001),脊柱侧凸患者中IL-6基因多态性的G/G基因型频率几乎是对照组的2倍(52.8%对26.2%,P<0.001)。MMP-3基因多态性的5A/5A基因型和IL-6基因多态性的G/G基因型分别独立地与脊柱侧凸风险较高相关(优势比分别为3.34和10.54)。

结论

这是第一项评估IL-6和MMPs基因变异可能与脊柱侧凸相关的可能性的研究,并表明MMP-3和IL-6启动子多态性是脊柱侧凸遗传易感性的重要因素。

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