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Serotonin Transporter (5-HTT) Gene Polymorphisms and Susceptibility to Epilepsy: A Meta-Analysis and Meta-Regression

机译:血清素转运蛋白(5-HTT)基因多态性和易感性癫痫:荟萃分析和荟萃回归。

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摘要

Aims: Serotonin transporter (5-HTT) plays a central role in the regulation of serotonin (5-hydroxytryptamine [5-HT]) synaptic function. Disturbances in 5-HT transmission are the most frequently reported neurobiological substrates of suicidal behavior. Emerging evidence has shown that the common polymorphisms in the 5-HTT gene may contribute to the risk of epilepsy, but individually published studies showed inconclusive results. This meta-analysis aimed to derive a more precise estimation of the associations between 5-HTT gene polymorphisms and susceptibility to epilepsy. Methods: A literature search of PubMed, Embase, Web of Science, and China BioMedicine (CBM) databases was conducted on articles published before June 1st, 2013. Crude odds ratios with 95% confidence intervals were calculated. Results: Seven studies were assessed with a total 1303 epilepsy patients and 1288 healthy controls. The meta-analysis results indicated that there was no significant relationship between 5-HTT gene polymorphisms and an increased risk of epilepsy. Further subgroup analysis based on ethnicity also found no significant association between 5-HTT gene polymorphisms and epilepsy risk among both Caucasian and Asian populations. In addition, there was also no significant association between 5-HTT gene polymorphisms and the risk of psychiatric comorbidity in patients with epilepsy. Conclusion: In conclusion, the current meta-analysis indicates that 5-HTT gene polymorphisms might not be the primary determinants of epilepsy susceptibility. 5-HTT genes might be expected to interact with other genes in different signaling pathways to initiate and promote the epileptogenic process.
机译:目的:5-羟色胺转运蛋白(5-HTT)在5-羟色胺(5-羟色胺[5-HT])突触功能的调节中起着核心作用。 5-HT传递障碍是自杀行为的最常报道的神经生物学底物。新兴证据表明,5-HTT基因常见的多态性可能会导致癫痫的风险,但个别发表的研究结果尚无定论。该荟萃分析旨在更准确地估计5-HTT基因多态性与癫痫易感性之间的关联。方法:对2013年6月1日之前发表的文章进行PubMed,Embase,Web of Science和China BioMedicine(CBM)数据库的文献检索。计算出具有95%置信区间的原油比值比。结果:共对130例癫痫患者和1288例健康对照者进行了七项研究评估。荟萃分析结果表明5-HTT基因多态性与癫痫风险增加之间没有显着关系。进一步的基于种族的亚组分析也未发现白种人和亚裔人群中5-HTT基因多态性与癫痫风险之间存在显着关联。此外,癫痫患者5-HTT基因多态性与精神病合并症的风险之间也没有显着关联。结论:总之,当前的荟萃分析表明5-HTT基因多态性可能不是癫痫易感性的主要决定因素。 5-HTT基因可能会在不同的信号传导途径中与其他基因相互作用,从而启动并促进癫痫发生过程。

著录项

  • 来源
    《Genetic testing and molecular biomarkers》 |2013年第12期|890-897|共8页
  • 作者单位

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery, Second Affiliated Hospital of Dalian Medical University, Dalian, China;

    Department of Neurosurgery Second Affiliated Hospital of Dalian Medical University Zhongshan Road No. 467 Dalian 116023 China;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 13:17:40

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