I型胶原蛋白在椎间盘退变中的作用

Z. A. Nurgaliev, V. V. Trefilova, M. Al-Zamil, N. A. Shnayder
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引用次数: 0

摘要

椎间盘退变(IDD)是导致慢性腰痛(LBP)的主要结构基质之一。腰痛是一种常见的神经系统疾病,但腰痛的遗传预测因素尚未得到充分研究。胶原纤维是髓核、纤维环和椎终板的重要组成部分。I型胶原作为椎间盘髓核和纤维环的结构成分被研究得最多。编码I型胶原α -1和α -2链的基因的单核苷酸变异(SNVs)与IDD相关,但遗传学研究的结果并未转化为行动。(1)本研究的目的是分析COL1基因家族在IDD和LBP发病中的关联遗传和全基因组研究。COL1A1基因SNVs与IDD相关性的研究对于个性化神经病学研究具有重要意义。个性化的方法可以帮助识别IDD发展及其并发症的高风险患者,包括年轻和工作年龄患者的椎间盘突出和椎管狭窄。另一方面,营养支持对COL1A1基因SNV风险等位基因携带者(包括胶原水解物和羟脯氨酸制剂)的作用尚未得到充分研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Role of Type I Collagen in Intervertebral Disc Degeneration
The intervertebral discs degeneration (IDD) is one of the leading structural substrates, causing chronic low back pain (LBP). LBP is a common neurological disorder but the LPB genetic predictors have not been sufficiently studied. Fibril collagens are important components of the nucleus pulposus, the anulus fibrosus and the vertebral endplate. Collagen type I is most studied as a structural component of the nucleus pulposus and the anulus fibrosus of the intervertebral disc. Single nucleotide variants (SNVs) of genes encoding alpha-1 and alpha-2 chains of collagen type I are associated with IDD, but the results of genetical studies are not translated into action. (1) The purpose of the study is the analysis of associative genetic and genome-wide studies of the COL1 gene family role in the development of IDD and LBP. The study of the COL1A1 gene’s SNVs association of with the IDD is important for the perspective of personalized neurology. A personalized approach can help to identify patients at high risk of the IDD developing and its complications, including intervertebral disc herniation and spinal stenoses in young and working age patients. On the other hand, the role of nutritional support for patients, carriers of the SNV risk alleles in the COL1A1 gene, including collagen hydrolysates and oxyproline preparations has not been sufficiently studied.
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