Abstract

BackgroundConsidered as one of the major causes of low back pain, Intervertebral disc degeneration (IVDD) is caused by several genetic and environmental factors. As inflammation plays an important role in disc degeneration, the genetic changes in both inflammatory and anti-inflammatory genes may play causative roles in IVDD as well. Therefore, the interactions between inflammatory and anti-inflammatory cytokines and also other components of disc matrix would determine the degree of tissue destruction in disc degeneration. However, there is still controversy regarding the exact role of inflammation and disc homeostasis imbalance in pathophysiology of IVDD. Therefore, current study was conducted to investigate the role of IL-10 and TGF-β single nucleotide polymorphisms (SNP) in Iranian IVDD patients.MethodsSeventy-six IVDD patients and 140 healthy controls were enrolled in this study. Genomic DNA from peripheral leukocytes was tested for 3 SNPs in IL10 (L-10 -1082G/A (rs1800896), IL-10 -819C/T (rs1800871), IL-10 -592A/C (rs1800872)) and 2 SNPs in TGF-β (TGF-β Codon 10 C/T (rs1982037), and TGF-β Codon 25 C/T (rs1800471) genes through PCR-SSP method. The extracted genomic DNA was genotyped for the aforementioned SNPs of interest using specific primers, which were coated in the cytokines KITs and based on the PCR-SSP method for sequencing.ResultsThe ‘T’ allele of IL-10 -819C/T and the ‘C’ allele of IL-10 -592A/C were more prevalent among patients, whereas the ‘C’ and ‘A’ alleles of respective SNPs were significantly more frequent in controls. The genotypes including ‘CT’ of IL-10 -819C/T, ‘CA’ of IL-10 -592A/C, and ‘GA’ of IL-10 -1082A/G were more common among patients, while the ‘CC’ genotype of both IL-10 -819C/T and IL-10 -592A/C SNPs were more frequent in controls. In addition, the IL-10 haplotypes including ‘ACC’, ‘ATA’, and ‘ACA’ were significantly associated with disease. Meanwhile, the ‘TC’ haplotype of TGF-β was more common among patients as well.ConclusionsThe IL-10 SNPs were significantly associated with IVDD in Iranian population; which proposes that genomic alterations of anti-inflammatory cytokines could lead to homeostasis imbalance in intervertebral discs and degenerative changes.

Highlights

  • Considered as one of the major causes of low back pain, Intervertebral disc degeneration (IVDD) is caused by several genetic and environmental factors

  • Study design and setting In order to investigate the association between IVDD and single nucleotide polymorphisms (SNP) in IL10 and Transforming Growth Factor β (TGF-β) genes, the current casecontrol study was designed according to the STROBE guideline for observational studies

  • Patient selection Over a two-year study period, adult patients with at least 6-month history of chronic low back pain who were diagnosed with intervertebral disc degeneration by two independent neurosurgeons, irresponsive to medical treatment and indicated for surgical intervention were included in this study

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Summary

Introduction

Considered as one of the major causes of low back pain, Intervertebral disc degeneration (IVDD) is caused by several genetic and environmental factors. As inflammation plays an important role in disc degeneration, the genetic changes in both inflammatory and anti-inflammatory genes may play causative roles in IVDD as well. There is still controversy regarding the exact role of inflammation and disc homeostasis imbalance in pathophysiology of IVDD. Comprising a disabling age-related health problem among middle-aged population, intervertebral disc degeneration (IVDD) is of the main causes of low back pain. Considering the multifactorial nature of disease, both genetic and environmental factors, as well as their interactions, may play causative roles in etiology of IVDD. In addition to alteration in the expression pattern of numerous genes, gene mutations and single nucleotide polymorphisms (SNP) could participate in etiology of degenerative changes in this disease [1, 4]

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