Genetic Polymorphisms of Interleukin-1 Alpha and the Vitamin D Receptor in Mexican Mestizo Patients with Intervertebral Disc Degeneration. (20th November 2014)

• Record Type: Journal Article
• Authors: Cervin Serrano, Salvador; González Villareal, Dalia; Aguilar-Medina, Maribel; Romero-Navarro, Jose Guillermo; Romero Quintana, Jose Geovanni; Arámbula Meraz, Eliakym; Osuna Ramírez, Ignacio; Picos-Cárdenas, Veronica; Granados, Julio; Estrada-García, Iris; Sánchez-Schmitz, Guzman; Ramos-Payán, Rosalío
• Other Names: Salem Mohamed Academic Editor.
• Is Part Of: International journal of genomics. Volume 2014(2014)
• Publication Date: 2014-11-20
• Subjects: Genomes -- Periodicals; Genomics -- Periodicals; Cytogenetics -- Periodicals; Genomics; Genome; Molecular Biology; Cytogenetics; Genomes; Genomics; Periodicals; 572.86
• DOI: 10.1155/2014/302568
• Languages: English
• ISSNs: 2314-436X

Abstract

Abstract : 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.