The role of smoking status and collagen IX polymorphisms in the susceptibility to cervical spondylotic myelopathy

被引:26
作者
Wang, Z. C. [2 ]
Shi, J. G. [1 ]
Chen, X. S. [1 ]
Xu, G. H. [1 ]
Li, L. J. [1 ]
Jia, L. S. [1 ]
机构
[1] Second Mil Med Univ, Changzheng Hosp, Dept Orthoped, Shanghai, Peoples R China
[2] Shanghai Jiao Tong Univ, Xinhua Hosp Chongming, Dept Orthoped, Shanghai 200030, Peoples R China
关键词
Smoking; Polymorphisms; Cervical spondylotic myelopathy; Collagen IX; DISC DEGENERATION; INTERVERTEBRAL DISCS; ARTICULAR-CARTILAGE; RISK-FACTOR; DISEASE; SEVERITY; BEARING; COL9A2; ALLELE; MODEL;
D O I
10.4238/2012.May.9.2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We investigated a possible association of collagen IX tryptophan (Trp) alleles (Trp2 and Trp3) and smoking with cervical spondylotic myelopathy (CSM) in 172 Chinese patients and 176 age-and gender-matched controls. The smoking status was evaluated by smoking index (SI). The CSM cases had a significantly higher prevalence of Trp2 alleles (Trp2+) than controls (19.8 vs 6.2%, P = 0.002), but the prevalence of Trp3 alleles (Trp3+) was similar between the two groups (23.3 vs 21.6%, P = 0.713). Logistic regression analyses showed that the subjects with Trp2+ had a higher risk for CSM. We thus analyzed whether smoking status influenced the association between Trp2 alleles and CSM risk. Among Trp2+ subjects with an SI less than 100, the smoking status did not influence the effect of risk for SCM [odds ratio (OR) = 1.34, 95% confidential interval (95%CI) = 0.85-2.18, P > 0.05]. When SI increased from 101 to 300, the OR for CSM reached 3.34 (95%CI = 2.11-5.67, P = 0.011); when SI was more than 300, the OR for CSM reached 5.56 (95%CI = 3.62-7.36, P < 0.001). Among Trp2-subjects with SI more than 300, the OR for CSM increased 2.14 (95%CI = 1.15-4.07, P = 0.024). We found a significant association between the Trp2 alleles and CSM risk and smoking amplifies this risk, suggesting that smoking abstinence is important for reducing CSM occurrence in subjects with high genetic risk.
引用
收藏
页码:1238 / 1244
页数:7
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