Liu J J, Wang W, Meng M, Liang C S, Zhang J W
Department of Neurology, The First Affiliated Hospital of Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Department of Clinical Medicine, Qiqihar Medical University, Qiqihar, Heilongjiang, China.
Genet Mol Res. 2016 Jul 14;15(2):gmr8349. doi: 10.4238/gmr.15028349.
Although various individual studies have evaluated the correlation between monoamine oxidase B (MAOB), polymorphism, and Parkinson's disease (PD), the results remain inconclusive. Therefore, we performed a meta-analysis in the Chinese population to provide comprehensive data on the association between the MAOB polymorphism and PD. Eligible studies were identified via databases such as PubMed, Springer Link, Ovid, Chinese Wanfang Data Knowledge Service Platform, Chinese National Knowledge Infrastructure, and Chinese Biology Medicine, throughout November 2015. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were used to assess the strengths of these associations. Eight studies documenting a total of 1385 cases of PD and 1426 controls were included in this meta-analysis. Overall, no significant association was found between the MAOB A644G polymorphism and PD risk in the Chinese population. However, in subgroup analyses, where results were stratified by geographical areas and source of controls, increased risk for PD in Northern China was observed (allele A vs G: OR = 1.33, 95%CI = 1.11-1.58; AA vs GG: OR = 1.46, 95%CI = 1.09-1.97; AA + AG vs GG: OR = 1.42, 95%CI = 1.06-1.90). Similarly, population-based studies also showed significant association between the MAOB A644G polymorphism and PD risk among different populations (allele A vs G: OR = 1.29, 95%CI = 1.11-1.51; AA vs GG: OR = 1.41, 95%CI = 1.09-1.82; AA + AG vs GG: OR = 1.34, 95%CI = 1.04- 1.71). In conclusion, this meta-analysis provided evidence that the MAOB A644G polymorphism may contribute to PD development in Northern China. Further studies conducted in other ethnic groups are required for definite conclusions.
尽管已有多项独立研究评估了单胺氧化酶B(MAOB)基因多态性与帕金森病(PD)之间的相关性,但其结果仍无定论。因此,我们在中国人群中进行了一项荟萃分析,以提供关于MAOB基因多态性与PD之间关联的全面数据。通过PubMed、Springer Link、Ovid、中国万方数据知识服务平台、中国知网和中国生物医学数据库等,检索截至2015年11月的相关研究。采用合并比值比(OR)和95%置信区间(CI)评估这些关联的强度。本荟萃分析纳入了8项研究,共涉及1385例PD患者和1426例对照。总体而言,在中国人群中,未发现MAOB A644G基因多态性与PD风险之间存在显著关联。然而,在按地理区域和对照来源分层的亚组分析中,发现中国北方PD风险增加(等位基因A与G:OR = 1.33,95%CI = 1.11 - 1.58;AA与GG:OR = 1.46,95%CI = 1.09 - 1.97;AA + AG与GG:OR = 1.42,95%CI = 1.06 - 1.90)。同样,基于人群的研究也显示,MAOB A644G基因多态性与不同人群的PD风险之间存在显著关联(等位基因A与G:OR = 1.29,95%CI = 1.11 - 1.51;AA与GG:OR = 1.41,95%CI = 1.09 - 1.82;AA + AG与GG:OR = 1.34,95%CI = 1.04 - 1.71)。总之,本荟萃分析提供了证据表明MAOB A644G基因多态性可能与中国北方PD的发生有关。需要在其他种族群体中进行进一步研究以得出明确结论。