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Nat Rev Rheumatol. 2014 Jan;10(1):44-56. doi: 10.1038/nrrheum.2013.160. Epub 2013 Oct 29.
2
Role of the promoter polymorphism IL-6 -174G/C in dermatomyositis and systemic lupus erythematosus.启动子多态性 IL-6-174G/C 在皮肌炎和系统性红斑狼疮中的作用。
Biomed Res Int. 2013;2013:315365. doi: 10.1155/2013/315365. Epub 2013 Sep 11.
3
The pro- and anti-inflammatory properties of the cytokine interleukin-6.细胞因子白细胞介素-6的促炎和抗炎特性。
Biochim Biophys Acta. 2011 May;1813(5):878-88. doi: 10.1016/j.bbamcr.2011.01.034. Epub 2011 Feb 4.
4
Association study of BMP4, IL6, Leptin, MMP3, and MTNR1B gene promoter polymorphisms and adolescent idiopathic scoliosis.骨形态发生蛋白 4、白细胞介素 6、瘦素、基质金属蛋白酶 3 和 MTNR1B 基因启动子多态性与青少年特发性脊柱侧凸的相关性研究。
Spine (Phila Pa 1976). 2011 Jan 15;36(2):E123-30. doi: 10.1097/BRS.0b013e318a511b0e.
5
Polymorphism in interleukin-6 gene is associated with bone mineral density in patients with adolescent idiopathic scoliosis.白细胞介素-6基因多态性与青少年特发性脊柱侧凸患者的骨密度相关。
J Bone Joint Surg Br. 2010 Aug;92(8):1118-22. doi: 10.1302/0301-620X.92B8.23676.
6
Lack of association between the promoter polymorphisms of MMP-3 and IL-6 genes and adolescent idiopathic scoliosis: a case-control study in a Chinese Han population.基质金属蛋白酶 3 和白细胞介素 6 基因启动子多态性与青少年特发性脊柱侧凸无关:一项中国汉族人群的病例对照研究。
Spine (Phila Pa 1976). 2010 Aug 15;35(18):1701-5. doi: 10.1097/BRS.0b013e3181c6ba13.
7
Association between IL-6 and MMP-3 gene polymorphisms and adolescent idiopathic scoliosis: a case-control study.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。
Spine (Phila Pa 1976). 2007 Nov 15;32(24):2700-2. doi: 10.1097/BRS.0b013e31815a5943.
8
Genetic association of complex traits: using idiopathic scoliosis as an example.复杂性状的基因关联:以特发性脊柱侧凸为例。
Clin Orthop Relat Res. 2007 Sep;462:38-44. doi: 10.1097/BLO.0b013e3180d09dcc.
9
Human nucleus pulposis can respond to a pro-inflammatory stimulus.人类髓核能够对促炎刺激作出反应。
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10
Distributions of HLA class I alleles and haplotypes in Bulgarians--contribution to understanding the origin of the population.保加利亚人HLA I类等位基因和单倍型的分布——对理解该人群起源的贡献
Tissue Antigens. 2001 Mar;57(3):208-15. doi: 10.1034/j.1399-0039.2001.057003208.x.

白细胞介素-6基因在特发性脊柱侧凸发病机制中的作用。

Role of the IL-6 gene in the etiopathogenesis of idiopathic scoliosis.

作者信息

Nikolova Svetla, Dikova Milka, Dikov Dobrin, Djerov Assen, Dzhebir Gyulnas, Atanasov Ventseslav, Savov Alexey, Kremensky Ivo

机构信息

National Genetic Laboratory, Medical University-Sofia, 2 Zdrave Street, 1431 Sofia, Bulgaria.

University Orthopedic Hospital "Prof. Boycho Boychev", 56 Nikola Petkov Boulevard, 1614 Sofia, Bulgaria.

出版信息

Anal Cell Pathol (Amst). 2015;2015:621893. doi: 10.1155/2015/621893. Epub 2015 Jun 23.

DOI:10.1155/2015/621893
PMID:26199858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4493265/
Abstract

Scoliotic human nuclei pulposi can respond to exogenous proinflammatory stimuli by secreting increased amounts of interleukin-6 (IL-6). The G/C polymorphism of the promoter region of IL-6 gene influences levels and functional activity of the IL-6 protein. We conducted a case-control study of eighty patients with idiopathic scoliosis (IS) and one hundred sixty healthy unrelated gender-matched controls trying to investigate the association between IS and the IL-6 promoter polymorphism at -174 position (rs1800795 G/C) in Bulgarian population. Molecular detection of the IL-6 genotypes was performed by amplification followed by restriction technology. The statistical analysis was performed by Pearson's chi-squared test. Our case-control study revealed a statistically significant association between the IL-6 (-174 G/C) functional polymorphism and susceptibility to IS. In addition, a significant association between the IL-6 (-174 G/C) polymorphism and curve severity was detected. IL-6 gene could be considered as susceptibility and modifying factor of idiopathic scoliosis. The identification of molecular markers with diagnostic and prognostic value could be useful for early detection of children at risk for the development of scoliosis and for prognosis of the risk for a rapid deformity progression. That would facilitate the therapy decisions and early stage treatment of the patient with the least invasive procedures.

摘要

脊柱侧弯患者的髓核可通过分泌更多白细胞介素-6(IL-6)来对外源性促炎刺激作出反应。IL-6基因启动子区域的G/C多态性会影响IL-6蛋白的水平和功能活性。我们对80例特发性脊柱侧弯(IS)患者和160名健康的、性别匹配的无关对照者进行了一项病例对照研究,旨在探究保加利亚人群中IS与IL-6启动子-174位点(rs1800795 G/C)多态性之间的关联。通过扩增后限制性技术对IL-6基因型进行分子检测。采用Pearson卡方检验进行统计分析。我们的病例对照研究揭示了IL-6(-174 G/C)功能多态性与IS易感性之间存在统计学显著关联。此外,还检测到IL-6(-174 G/C)多态性与侧弯严重程度之间存在显著关联。IL-6基因可被视为特发性脊柱侧弯的易感性和修饰因子。鉴定具有诊断和预后价值的分子标志物可能有助于早期发现有脊柱侧弯发展风险的儿童,并对快速畸形进展风险进行预后评估。这将有助于做出治疗决策,并采用侵入性最小的程序对患者进行早期治疗。