Department of Human Genetics, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, 560029, India.
Armed Forces Medical College, Pune, 411040, India.
J Mol Neurosci. 2018 Nov;66(3):378-382. doi: 10.1007/s12031-018-1182-3. Epub 2018 Oct 4.
Lumbar disc degeneration (LDD) is a multifactorial disorder caused by genetic and environmental factors. Polymorphisms in several structural and inflammatory genes like collagens, aggrecan, matrix metalloproteinases are associated with the risk of disc degeneration. In this study, we analyzed the role of a few important single nucleotide polymorphisms in cartilage intermediate layer protein (CILP), collagen 9A2 (COL9A2) and matrix metalloproteinase 3 (MMP3) genes in LDD from an Indian population. Two hundred patients with LDD and 200 healthy controls were recruited for the study. Genotyping was performed by allelic discrimination assay. The rs2073711 polymorphism (CILP gene - GG genotype) was associated with reduced risk of LDD in the Indian population (OR = 0.43, p = 0.016). The rs591058 polymorphism (MMP3 gene - TT genotype) is found to be associated with lower risk among women (OR = 0.34, p = 0.041). No significant association was found between COL9A2 polymorphism rs7533552 and the risk of LDD. We conclude that the CILP gene polymorphism (rs2073711) is associated with a lower risk of LDD, the MMP3 (rs591058) gene polymorphism is associated with LDD among women, and the TT genotype confers a lower risk of LDD.
腰椎间盘退变(LDD)是一种由遗传和环境因素引起的多因素疾病。几种结构和炎症基因(如胶原蛋白、聚集蛋白聚糖、基质金属蛋白酶)的多态性与椎间盘退变的风险相关。在这项研究中,我们分析了软骨中间层蛋白(CILP)、胶原 9A2(COL9A2)和基质金属蛋白酶 3(MMP3)基因中的一些重要单核苷酸多态性在印度人群中 LDD 中的作用。招募了 200 名 LDD 患者和 200 名健康对照者进行研究。通过等位基因鉴别分析进行基因分型。rs2073711 多态性(CILP 基因-GG 基因型)与印度人群 LDD 风险降低相关(OR=0.43,p=0.016)。rs591058 多态性(MMP3 基因-TT 基因型)在女性中与较低的风险相关(OR=0.34,p=0.041)。COL9A2 多态性 rs7533552 与 LDD 风险之间无显著关联。我们得出结论,CILP 基因多态性(rs2073711)与 LDD 的较低风险相关,MMP3(rs591058)基因多态性与女性的 LDD 相关,TT 基因型使 LDD 的风险降低。