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Association of COL2A1 Gene Polymorphism with Degenerative Lumbar Scoliosis
Clinics in Orthopedic Surgery ; : 379-384, 2014.
Artigo em Inglês | WPRIM | ID: wpr-223889
ABSTRACT

BACKGROUND:

Degenerative lumbar scoliosis (DLS) progresses with aging after 50-60 years, and the genetic association of DLS remains largely unclear. In this study, the genetic association between collagen type II alpha 1 (COL2A1) gene and DLS was investigated.

METHODS:

COL2A1 gene polymorphism was investigated in DLS subjects compared to healthy controls to investigate the possibility of its association with COL2A1 gene. Based on a single nucleotide polymorphism (SNP) database, SNP (rs2276454) in COL2A1 were selected and genotyped using direct sequencing in 51 patients with DLS and 235 healthy controls. The SNP effects were analyzed using three models of codominant, dominant, and recessive. Logistic regression models were calculated for odds ratios (ORs) with 95% confidence intervals (CIs) and corresponding p-values, controlling age and gender as co-variables.

RESULTS:

SNP (rs2276454) in COL2A1 was significantly associated with the degenerative lumbar scoliosis in the codominant (OR, 1.90; 95% CI, 1.17 to 3.10; p = 0.008) and dominant models (OR, 3.58; 95% CI, 1.59 to 9.29; p = 0.001).

CONCLUSIONS:

The results suggest that COL2A1 is associated with the risk of DLS in Korean population.
Assuntos

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Escoliose / Polimorfismo de Nucleotídeo Único / Colágeno Tipo II / Povo Asiático / Vértebras Lombares Limite: Idoso / Feminino / Humanos / Masculino Idioma: Inglês Revista: Clinics in Orthopedic Surgery Ano de publicação: 2014 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Escoliose / Polimorfismo de Nucleotídeo Único / Colágeno Tipo II / Povo Asiático / Vértebras Lombares Limite: Idoso / Feminino / Humanos / Masculino Idioma: Inglês Revista: Clinics in Orthopedic Surgery Ano de publicação: 2014 Tipo de documento: Artigo