Association Between a Polymorphism of the Transforming Growth Factor-β1 Gene and Genetic Susceptibility to Ossification of the Posterior Longitudinal Ligament in Japanese Patients

Publisher Website
Google Scholar
Abstract
A study was conducted to determine the association between polymorphism of the transforming growth factor-β1 (TGF-β1) gene and ossification of the posterior longitudinal ligament (OPLL) prevalence. To examine whether the T869→C polymorphism of the TGF-β1 gene is associated with genetic susceptibility to OPLL in Japanese subjects. In the posterior longitudinal ligament, OPLL is associated with abnormal calcium metabolism. Several candidate genes are associated with the prevalence of OPLL. In the ossified matrix and chondrocytes of adjacent cartilaginous areas of OPLL, TGF-β1 is overexpressed. The TGF-β1 genotype was identified with an allele-specific polymerase chain reaction method in 319 Japanese subjects (46 subjects with OPLL and 273 control subjects). There was a significant association between the T869→C genotype and the prevalence of OPLL in the cervical spine. Multivariable logistic regression analysis, adjusted for gender, age, height, and body weight, showed that the frequency of the C allele was significantly higher in subjects with OPLL than in control subjects. The T869→C polymorphism of the TGF-β1 gene is a genetic determinant of a predisposition to OPLL, with the C allele representing a risk factor for genetic susceptibility to OPLL in Japanese subjects. Therefore, TGF-β1 genotyping may be useful in the prevention of OPLL.

This publication has 12 references indexed in Scilit: