Association of Toll-Like Receptor 5 Gene Polymorphism with Susceptibility to Ossification of the Posterior Longitudinal Ligament of the Spine in Korean Population.
- Author:
Won Suk CHUNG
1
;
Dong Hyun NAM
;
Dae Jean JO
;
Jun Hwan LEE
Author Information
- Publication Type:Original Article
- Keywords: OPLL; TLR5 gene; Polymorphisms; Genetic association study
- MeSH: Case-Control Studies; Chondrocytes; Clinical Coding; Collagen; Cytokines; Genetic Association Studies; Haplotypes; Humans; Intercellular Signaling Peptides and Proteins; Linkage Disequilibrium; Logistic Models; Longitudinal Ligaments; Morphogenesis; Odds Ratio; Ossification of Posterior Longitudinal Ligament; Polymorphism, Single Nucleotide; Spine; Toll-Like Receptor 5; Toll-Like Receptors
- From:Journal of Korean Neurosurgical Society 2011;49(1):8-12
- CountryRepublic of Korea
- Language:English
- Abstract: OBJECTIVE: Ossification of the posterior longitudinal ligament (OPLL) has a strong genetic component. Specific gene polymorphisms may be associated with OPLL in several genes which regulate calcification in chondrocytes, change of extracellular collagen matrix and secretions of many growth factors and cytokines controlling bone morphogenesis. Toll-like receptor 5 (TLR5) may play a role in the pathogenesis of OPLL by intermediate nuclear factor-kappa B (NF-kappaB). The current study focused on coding single nucleotide polymorphisms (SNPs) of TLR5 for a case-control study investigating the relationship between TLR5 and OPLL in a Korean population. METHODS: A total of 166 patients with OPLL and 231 controls were recruited for a case-control association study investigating the relationship between SNPs of TLR5 gene and OPLL. Four SNPs were genotyped by direct sequencing (rs5744168, rs5744169, rs2072493, and rs5744174). SNP data were analyzed using the SNPStats, SNPAnalyzer, Haploview, and Helixtree programs. Multiple logistic regression analysis with adjustment for age and gender was performed to calculate an odds ratio (OR). RESULTS: None of SNPs were associated with OPLL in three alternative models (codominant, dominant, and recessive models; p > 0.05). A strong linkage disequilibrium block, including all 4 SNPs, was constructed using the Gabriel method. No haplotype was significantly associated with OPLL in three alternative models. CONCLUSION: These results suggest that Toll-like receptor 5 gene may not be associated with ossification of the posterior longitudinal ligament risk in Korean population.
