Literature DB >> 26656061

Association Between IL-6 and MMP3 Common Genetic Polymorphisms and Idiopathic Scoliosis in Bulgarian Patients: A Case-control Study.

Svetla Todorova Nikolova1, Vasil Tsankov Yablanski, Evgeni Nedev Vlaev, Luben Dimitrov Stokov, Alexey Slavkov Savov, Ivo Marinov Kremensky, Alexandre Roumenov Loukanov.   

Abstract

STUDY
DESIGN: A case-control study was performed on 105 patients with idiopathic scoliosis (IS) and 210 unrelated gender-matched controls from Bulgarian population.
OBJECTIVE: Investigation of the association between common genetic polymorphisms of IL-6 and MMP3 genes and the etiology and progression of IS among Bulgarian patients. SUMMARY OF BACKGROUND DATA: The IL-6 and MMP3 genes have been considered as candidate genes of IS in Caucasian population.
METHODS: Molecular detection of the promoter polymorphisms of IL-6 and MMP3 was performed by polymerase chain reaction followed by restriction fragment length polymorphism. The statistical analysis was performed by χ test with a value of P < 0.05 as statistically significant. The combinatorial effect of the candidate genes was also examined.
RESULTS: This case-control study revealed statistically significant association between the IL-6 (rs1800795) functional polymorphism and susceptibility to IS (χ = 16.055; P < 0.0001). In addition, a significant association between IL-6 (rs1800795) and curve severity was detected (χ = 16.87; P < 0.0001). No genotype or allele of MMP3 (rs3025058) was found to be correlated to the onset or progression of IS (P > 0.05). One IL-6-MMP3 genotype combination was associated with the susceptibility to IS.
CONCLUSION: IL-6 gene could be considered as a susceptibility and modifying factor of IS. The identification of molecular markers with diagnostic and prognostic value could be useful for early detection of children at risk for the development of IS and for prognosis of the risk for a rapid deformity progression. That would facilitate the therapy decisions and early stage treatment of the patient with the least invasive procedures. LEVEL OF EVIDENCE: 4.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 26656061     DOI: 10.1097/BRS.0000000000001360

Source DB:  PubMed          Journal:  Spine (Phila Pa 1976)        ISSN: 0362-2436            Impact factor:   3.468


  4 in total

1.  Positive association between a polymorphic locus near the LBX1 gene and predisposition of idiopathic scoliosis in Southeastern European population.

Authors:  Svetla Nikolova; Milka Dikova; Dobrin Dikov; Assen Djerov; Alexey Savov; Ivo Kremensky; Alexandre Loukanov
Journal:  J Appl Biomed       Date:  2019-07-04       Impact factor: 1.797

Review 2.  Predictive value of single-nucleotide polymorphisms in curve progression of adolescent idiopathic scoliosis.

Authors:  Wengang Wang; Tailong Chen; Yibin Liu; Songsong Wang; Ningning Yang; Ming Luo
Journal:  Eur Spine J       Date:  2022-04-17       Impact factor: 2.721

3.  Lack of association between AKAP2 and the susceptibility of adolescent idiopathic scoliosis in the Chinese population.

Authors:  Leilei Xu; Chao Xia; Weiguo Zhu; Zhenhua Feng; Xiaodong Qin; Weixiang Sun; Yong Qiu; Zezhang Zhu
Journal:  BMC Musculoskelet Disord       Date:  2017-08-24       Impact factor: 2.362

4.  Exploring the association between specific genes and the onset of idiopathic scoliosis: a systematic review.

Authors:  Sergio De Salvatore; Laura Ruzzini; Umile Giuseppe Longo; Martina Marino; Alessandra Greco; Ilaria Piergentili; Pier Francesco Costici; Vincenzo Denaro
Journal:  BMC Med Genomics       Date:  2022-05-19       Impact factor: 3.063

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.