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Genetic Polymorphisms of Interleukin-1 Alpha and the Vitamin D Receptor in Mexican Mestizo Patients with Intervertebral Disc Degeneration

机译:墨西哥Mestizo椎间盘退变患者中白细胞介素-1α和维生素D受体的遗传多态性

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摘要

Intervertebral disc degeneration (IDD) is the most common diagnosis in patients with back pain, a leading cause of musculoskeletal disability worldwide. Several conditions, such as occupational activities, gender, age, and obesity, have been associated with IDD. However, the development of this disease has strong genetic determinants. In this study, we explore the possible association between rs1800587 (c.-949C>T) of interleukin-1 alpha (IL1A) and rs2228570 (c.2T>V) and rs731236 (c.1056T>C) of vitamin D receptor (VDR) gene polymorphisms and the development of IDD in northwestern Mexican Mestizo population. Gene polymorphisms were analyzed by polymerase chain reaction followed by restriction fragment length polymorphism, in two groups matched by age and gender: patients with symptomatic lumbar IDD (n = 100) and subjects with normal lumbar-spine MRI-scans (n = 100). Distribution of the mutated alleles in patients and controls was 27.0% versus 28.0% (P = 0.455) for T of rs1800587 (IL1A); 53.0% versus 58.0% (P = 0.183) for V of rs2228570 (VDR); and 18.0% versus 21.0% (P = 0.262) for C of rs731236 (VDR). Our results showed no association between the studied polymorphisms and IDD in this population. This is the first report on the contribution of gene polymorphisms on IDD in a Mexican population.
机译:椎间盘退变(IDD)是背痛患者的最常见诊断,背痛是全世界肌肉骨骼失能的主要原因。某些疾病,例如职业活动,性别,年龄和肥胖与IDD相关。但是,这种疾病的发展具有很强的遗传决定因素。在这项研究中,我们探讨了维生素D受体的白细胞介素1α(IL1A)的rs1800587(c.-949C> T)与rs2228570(c.2T> V)和rs731236(c.1056T> C)之间的可能联系( VDR)基因多态性与墨西哥西北混血儿群体IDD的发展。通过聚合酶链反应和限制性片段长度多态性分析基因多态性,按年龄和性别分为两组:有症状腰椎IDD患者(n = 100)和具有正常腰椎MRI扫描(n = 100)的受试者。 rs1800587(IL1A)的T患者中突变的等位基因在患者和对照组中的分布为27.0%,而28.0%(P = 0.455); rs2228570(VDR)的V分别为53.0%和58.0%(P = 0.183); rs731236(VDR)的C分别为18.0%和21.0%(P = 0.262)。我们的结果表明,该人群中研究的多态性与IDD之间没有关联。这是关于墨西哥人群IDD基因多态性贡献的第一份报告。

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