Department of Neurosurgery, J. W. Goethe University, Frankfurt am Main, Germany.
J Neurosurg Spine. 2009 Dec;11(6):659-66. doi: 10.3171/2009.7.SPINE08667.
The authors examined a possible association between apolipoprotein E (APOE) gene polymorphism and the outcome after anterior microsurgical decompression in patients with cervical spondylotic myelopathy (CSM).
The authors conducted a prospective study of 60 consecutive patients (40 men, 20 women) with CSM who underwent anterior microsurgical decompression. The patients ranged in age from 26 to 86 years (mean 61.5 +/- 14.6 years). Neurological deficits were classified according to the modified Japanese Orthopaedic Association Scale. Mean follow-up was 18.8 +/- 4.6 months and APOE genotyping was carried out by isolation of DNA from venous blood samples. The APOE genotypes were determined by polymerase chain reaction followed by restriction enzyme digestion and polyacrylamide gel electrophoresis of digested fragments. Categorical variables were analyzed with the chi-square test, continuous data with the Mann-Whitney U-test, and for multiple groups with the Kruskal-Wallis H-test. A backward stepwise binary logistic regression analysis was performed to determine the effect of APOE in a multivariate model.
Of the 60 patients with CSM, 35 (58.3%) improved and 25 (41.7%) did not improve or suffered deterioration (no-improvement group). In the improvement group 5 patients (8.3%) possessed the epsilon4 allele compared with 16 patients (26.7%) in the no-improvement group (p = 0.002, OR 3.3, 95% CI 1.7-6.1). In a multivariate model, the occurrence of the epsilon4 allele was a significant independent predictor for no improvement after anterior decompression and fusion (p = 0.004, OR 8.6, 95% CI 5.1-20.6).
The results of this study show that APOE gene polymorphism influences the short-term outcome of CSM patients after surgical decompressive and stabilizing therapy in the way that the presence of the APOE epsilon4 allele is an independent predictor for a no improvement. The presence of APOE may explain in part the different responses to operative therapies in patients with cervical myelopathy.
作者研究了载脂蛋白 E(APOE)基因多态性与颈椎脊髓病(CSM)患者前路显微减压术后结局之间的可能关联。
作者对 60 例连续行前路显微减压术的 CSM 患者进行了前瞻性研究。患者年龄 26 岁至 86 岁,平均 61.5±14.6 岁。神经功能缺损根据改良日本矫形协会量表进行分类。平均随访时间为 18.8±4.6 个月,采用静脉血样 DNA 分离法进行 APOE 基因分型。APOE 基因型通过聚合酶链反应(PCR)后限制性内切酶消化和消化产物的聚丙烯酰胺凝胶电泳确定。采用卡方检验分析分类变量,采用曼-惠特尼 U 检验分析连续变量,采用 Kruskal-Wallis H 检验分析多组变量。采用向后逐步二项逻辑回归分析在多变量模型中确定 APOE 的作用。
60 例 CSM 患者中,35 例(58.3%)改善,25 例(41.7%)无改善或恶化(无改善组)。在改善组中,5 例(8.3%)携带 epsilon4 等位基因,而在无改善组中,16 例(26.7%)携带 epsilon4 等位基因(p=0.002,OR3.3,95%CI1.7-6.1)。在多变量模型中,epsilon4 等位基因的出现是前路减压融合术后无改善的显著独立预测因子(p=0.004,OR8.6,95%CI5.1-20.6)。
本研究结果表明,APOE 基因多态性影响 CSM 患者手术减压和稳定治疗后的短期结局,APOEepsilon4 等位基因的存在是无改善的独立预测因子。APOE 的存在部分解释了颈椎脊髓病患者对手术治疗的不同反应。