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

Author:

Cervin Serrano Salvador1,González Villareal Dalia2,Aguilar-Medina Maribel2,Romero-Navarro Jose Guillermo2,Romero Quintana Jose Geovanni2,Arámbula Meraz Eliakym2,Osuna Ramírez Ignacio2,Picos-Cárdenas Veronica3,Granados Julio4,Estrada-García Iris5,Sánchez-Schmitz Guzman6,Ramos-Payán Rosalío27

Affiliation:

1. Division of Pain, ISSSTE Hospital, 80200 Culiacán, SIN, Mexico

2. Faculty of Biological and Chemical Sciences, Doctoral Programs in Biotechnology and Biomedical Sciences, Autonomous University of Sinaloa, 80010 Culiacán, SIN, Mexico

3. Human Genetics Laboratory of the Research Unit, Faculty of Medicine, Autonomous University of Sinaloa, 80019 Culiacán, SIN, Mexico

4. Division of Immunogenetics, National Institute of Medical Sciences and Nutrition, 14000 Mexico City, DF, Mexico

5. Department of Immunology, National School of Biological Science, National Polytechnic Institute, 11340 Mexico City, DF, Mexico

6. Division of Infectious Diseases, Boston Children’s Hospital and Harvard Medical School, Harvard University, Boston, MA 02115, USA

7. Laboratory of Immunology, Faculty of Biological and Chemical Sciences, Autonomous University of Sinaloa, Avenida de las Américas y Universitarios s/n, Ciudad Universitaria, 80010 Culiacán, SIN, Mexico

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 IDDn=100and subjects with normal lumbar-spine MRI-scansn=100. Distribution of the mutated alleles in patients and controls was 27.0% versus 28.0%P=0.455for T of rs1800587 (IL1A); 53.0% versus 58.0%P=0.183for V of rs2228570 (VDR); and 18.0% versus 21.0%P=0.262for 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.

Funder

Consejo Nacional de Ciencia y Tecnología

Publisher

Hindawi Limited

Subject

Pharmaceutical Science,Genetics,Molecular Biology,Biochemistry

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