Duan Chunhong, Wang Meiyun, Zhang Yan, Wei Xuxia, Huang Yan, Zhang Hongxia, Cheng Lu, Gai Zhongtao
Ji'nan Children's Hospital, Ji'nan, Shandong, China.
Ji'nan Center For Disease Control And Prevention, Ji'nan, Shandong, China.
Am J Alzheimers Dis Other Demen. 2016 May;31(3):201-7. doi: 10.1177/1533317515602220. Epub 2015 Sep 3.
A meta-analysis was performed to better clarify the association between hemochromatosis (HFE) gene and the risk of Parkinson's disease (PD).
Pooled odds ratio (OR) with 95% confidence interval (CI) was calculated from fixed- and random-effect models. Heterogeneity among studies was evaluated using the I(2) and Q test. Egger's test was used to estimate the publication bias.
We identified 8 articles with 9 independent studies for this meta-analysis. The present meta-analysis showed no significant association of Y allele with the risk of PD in dominant (OR = 0.87, 95% CI = 0.70-1.09), recessive (OR = 1.58, 95% CI = 0.61-4.10), and codominant (OR = 0.88, 95% CI = 0.72-1.09) models for C282Y. There were also no significant associations of D allele with the risk of PD in dominant (OR = 1.04, 95% CI = 0.87-1.24), recessive (OR = 1.23, 95% CI = 0.70-2.18), and codominant (OR = 1.04, 95% CI = 0.89-1.22) genetic models for H63D. No publication bias was detected.
The meta-analysis indicated that C282Y and H63D polymorphisms in the HFE gene might not be associated with PD.
进行一项荟萃分析以更好地阐明血色素沉着症(HFE)基因与帕金森病(PD)风险之间的关联。
采用固定效应模型和随机效应模型计算合并比值比(OR)及其95%置信区间(CI)。使用I²和Q检验评估研究间的异质性。采用Egger检验评估发表偏倚。
我们为该荟萃分析确定了8篇文章,其中包含9项独立研究。本荟萃分析显示,在C282Y的显性(OR = 0.87,95%CI = 0.70 - 1.09)、隐性(OR = 1.58,95%CI = 0.61 - 4.10)和共显性(OR = 0.88,95%CI = 0.72 - 1.09)模型中,Y等位基因与PD风险无显著关联。在H63D的显性(OR = 1.04,95%CI = 0.87 - 1.24)、隐性(OR = 1.23,95%CI = 0.70 - 2.18)和共显性(OR = 1.04,95%CI = 0.89 - 1.22)遗传模型中,D等位基因与PD风险也无显著关联。未检测到发表偏倚。
荟萃分析表明,HFE基因中的C282Y和H63D多态性可能与PD无关。