Department of Orthopaedics, Peking Union Medical College Hospital, Beijing, People's Republic of China.
Eur Rev Med Pharmacol Sci. 2013 Jul;17(13):1830-4.
The present study aimed to determine whether the -735 C/T polymorphism of the Matrix Metalloproteinase 2 (MMP2) gene is associated with the risk and severity of lumbar disc degeneration (LDD) in the Chinese Han population.
A total of 1008 patients with LDD and 906 healthy controls were enrolled in this study. The grade of disc degeneration was determined according to Schneiderman's classification for Magnetic Resonance Imaging (MRI). The -735 C/T polymorphism of MMP2 was genotyped using polymerase chain reaction and the restriction fragment length polymorphism method.
The genotype frequency of the -735 C/T polymorphism was in agreement with the Hardy-Weinberg equilibrium (p = 0.087). The frequencies of the -735CT and TT genotypes were significantly lower among LDD patients compared with normal controls (p < 0.001); CT and TT genotype were significantly associated with a decreased risk of LDD compared with the CC genotype (for TT genotype, p = 0.031; OR 0.413; 95% CI 0.184-0.924; for CT genotype, p < 0.001, OR 0.645, 95% CI 0.506-0.822). Patients with LDD showed significantly higher frequencies of the C allele than normal controls (p < 0.001), T allele was significantly associated with a decreased risk of LDD compared with the C allele (p < 0.001; OR 0.631; 95% CI 0.508-0.783). In addition, the -735TT and CT genotypes, as well as the T allele were associated with lower degenerative grades of LDD compared with CC genotype and the C allele, respectively (both p < 0.001).
The -735 C/T polymorphism of MMP2 may be associated with the risk and severity of LDD in the Chinese Han population.
本研究旨在探讨基质金属蛋白酶 2(MMP2)基因-735 C/T 多态性与中国汉族人群腰椎间盘退变(LDD)的风险和严重程度是否相关。
本研究纳入了 1008 例 LDD 患者和 906 例健康对照者。根据磁共振成像(MRI)的 Schneiderman 分级标准确定椎间盘退变程度。采用聚合酶链反应和限制性片段长度多态性方法检测 MMP2-735 C/T 多态性。
-735 C/T 多态性的基因型频率符合 Hardy-Weinberg 平衡(p = 0.087)。与正常对照组相比,LDD 患者-735 CT 和 TT 基因型的频率显著降低(p < 0.001);与 CC 基因型相比,CT 和 TT 基因型与 LDD 的发病风险降低显著相关(TT 基因型,p = 0.031;OR 0.413;95%CI 0.184-0.924;CT 基因型,p < 0.001,OR 0.645,95%CI 0.506-0.822)。LDD 患者的 C 等位基因频率显著高于正常对照组(p < 0.001),T 等位基因与 LDD 的发病风险降低显著相关(p < 0.001;OR 0.631;95%CI 0.508-0.783)。此外,与 CC 基因型和 C 等位基因相比,-735 TT 和 CT 基因型以及 T 等位基因与 LDD 的较低退行性分级相关(均 p < 0.001)。
MMP2 基因-735 C/T 多态性可能与中国汉族人群 LDD 的发病风险和严重程度相关。