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机构地区:[1]Department of Neurology,Tongji Hospital,Huazhong University of Science and Technology [2]Department of Neurosurgery,Tongji Hospital,Huazhong University of Science and Technology
出 处:《Journal of Huazhong University of Science and Technology(Medical Sciences)》2015年第5期635-639,共5页华中科技大学学报(医学英德文版)
基 金:supported by the National Natural Science Foundation of China for Young Scholars(No.81201006)
摘 要:Previous studies have reported the association of prodynorphin(PDYN) promoter polymorphism with temporal lobe epilepsy(TLE) susceptibility,but the results remain inconclusive. To further precisely evaluate this association,we performed a meta-analysis. Published studies of TLE and PDYN polymorphism up to February 2015 were identified. Subgroup analysis by TLE subtype was performed. Moreover,sensitivity,heterogeneity,and publication bias were also analyzed. Seven case-control studies were finally included in this meta-analysis with 875 TLE cases and 1426 controls. We did not find synthetic evidence of association between PDYN promoter polymorphism and TLE susceptibility(OR=1.184,95% CI: 0.873–1.606,P=0.277). Similar results were also obtained in non-familial-risk TLE subgroup. However,in the familial-risk TLE subgroup analysis,a significant association was observed(OR=1.739,95% CI: 1.154–2.619,P=0.008). In summary,this meta-analysis suggests that PDYN gene promoter polymorphism might contribute to familial-risk TLE.Previous studies have reported the association of prodynorphin(PDYN) promoter polymorphism with temporal lobe epilepsy(TLE) susceptibility,but the results remain inconclusive. To further precisely evaluate this association,we performed a meta-analysis. Published studies of TLE and PDYN polymorphism up to February 2015 were identified. Subgroup analysis by TLE subtype was performed. Moreover,sensitivity,heterogeneity,and publication bias were also analyzed. Seven case-control studies were finally included in this meta-analysis with 875 TLE cases and 1426 controls. We did not find synthetic evidence of association between PDYN promoter polymorphism and TLE susceptibility(OR=1.184,95% CI: 0.873–1.606,P=0.277). Similar results were also obtained in non-familial-risk TLE subgroup. However,in the familial-risk TLE subgroup analysis,a significant association was observed(OR=1.739,95% CI: 1.154–2.619,P=0.008). In summary,this meta-analysis suggests that PDYN gene promoter polymorphism might contribute to familial-risk TLE.
关 键 词:Epilepsy epilepsy familial Promoter promoter susceptibility Polymorphism subgroup heterogeneity Seven
分 类 号:R742.1[医药卫生—神经病学与精神病学]
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