From the Department of The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, People's Republic of China.
Spine (Phila Pa 1976). 2013 Dec 1;38(25):E1600-7. doi: 10.1097/BRS.0000000000000012.
Data on the association between the ACAN (encoded for aggrecan core protein) variable number of tandem repeat (VNTR) polymorphism and lumbar disc degeneration are conflicting, so we performed a meta-analysis.
Aggrecan is involved in the shock absorbing function of the lumbar disc; we performed a meta-analysis to assess the association between ACAN VNTR and lumbar degeneration.
To perform a meta-analysis, we searched for studies published until September 2012, using electronic databases (PubMed, EMBASE, and China National Knowledge Infrastructure). Eight studies involving 965 cases of lumbar disc degeneration and 982 control subjects were identified.
Assessment for eligibility and extraction of data were performed by 2 independent investigators. We extracted allele frequency for each study. We calculated the pooled odds ratios (ORs) and 95% confidence intervals (CI) to assess the strength of the association between the ACAN VNTR polymorphism and lumbar disc degeneration risk.
Results from the allele model suggested an increased risk of lumbar disc degeneration for the shorter alleles carriers compared with the normal alleles and longer alleles (OR = 1.54, 95% CI: 1.04-2.30, P = 0.03). In subgroup analysis by ethnicity, significant increased risks were found among Asians with shorter alleles (OR=1.65, 95% CI: 1.17-2.33, P = 0.004).
Our results suggest an increased risk of shorter alleles compared with normal alleles and longer alleles against lumbar disc degeneration among populations especially among Asian descent. Such association may not be statistically significant in European populations.
关于蛋白聚糖(核心蛋白)的串联重复(VNTR)多态性与腰椎间盘退变之间的关联,数据存在冲突,因此我们进行了荟萃分析。
蛋白聚糖参与腰椎间盘的减震功能;我们进行了荟萃分析,以评估 ACAN VNTR 与腰椎退变之间的关系。
为了进行荟萃分析,我们使用电子数据库(PubMed、EMBASE 和中国国家知识基础设施)搜索截至 2012 年 9 月发表的研究。确定了 8 项涉及 965 例腰椎间盘退变和 982 例对照的研究。
由 2 名独立研究者评估纳入标准和提取数据。我们提取了每个研究的等位基因频率。我们计算了汇总的优势比(OR)和 95%置信区间(CI),以评估 ACAN VNTR 多态性与腰椎间盘退变风险之间的关联强度。
等位基因模型的结果表明,与正常等位基因和较长等位基因相比,较短等位基因携带者发生腰椎间盘退变的风险增加(OR=1.54,95%CI:1.04-2.30,P=0.03)。按种族亚组分析,较短等位基因携带者的风险显著增加(OR=1.65,95%CI:1.17-2.33,P=0.004)。
我们的结果表明,与正常等位基因和较长等位基因相比,人群中尤其是亚洲人群的较短等位基因携带者发生腰椎间盘退变的风险增加。这种关联在欧洲人群中可能没有统计学意义。