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Angiotensln-Converting Enzyme Gene Polymorphism in Patients with Multiple Sclerosis from Bosnia and Herzegovina

机译:波斯尼亚和黑塞哥维那多发性硬化症患者的血管紧张素转换酶基因多态性

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摘要

Background: Increased activity of angiotensin-converting enzyme (ACE) in the blood and cerebrospinal fluid of patients with multiple sclerosis (MS), and the inhibition of ACE in experimental autoimmune encephalomyelitis, suggested that ACE may play a role in the pathogenesis and progression of MS. We recently published the first report on the potential association of MS and ACE I/D polymorphism in Slovenian and Croatian patients with MS, in which it was shown that the DD genotype might contribute to a higher risk of developing MS in men. To confirm these findings in a similar ethnic population, we analyzed ACE I/D gene polymorphism in patients with MS from Bosnia and Herzegovina. Subjects and Methods: One hundred and seventy patients with MS and 170 healthy controls were genotyped by the polymerase chain reaction method. Results: There was no significant difference in the distribution of ACE I/D genotypes (p=0.783) or in the allelic frequencies (p = 0.538) between patients with MS and control subjects. When patients with MS were stratified by sex, no statistically significant differences in allele or genotype distributions were observed. Finally, there was no indication of an impact of the ACE I/D genotype on disease course or severity. Conclusion: The ACE I/D polymorphism is not a risk factor for development of MS, nor does it contribute to disease severity in this Bosnia and Herzegovina population.
机译:背景:多发性硬化症(MS)患者血液和脑脊液中血管紧张素转换酶(ACE)的活性增加,以及实验性自身免疫性脑脊髓炎对ACE的抑制作用,提示ACE可能在脑血管病的发病和发展中起作用多发性硬化症。我们最近发表了关于斯洛文尼亚和克罗地亚MS患者中MS与ACE I / D多态性的潜在关联的第一份报告,其中显示DD基因型可能导致男性罹患MS的风险更高。为了证实在类似种族中的这些发现,我们分析了波斯尼亚和黑塞哥维那MS患者的ACE I / D基因多态性。研究对象和方法:采用聚合酶链反应法对一百零七名MS患者和170名健康对照者进行基因分型。结果:MS患者与对照组之间的ACE I / D基因型分布(p = 0.783)或等位基因频率(p = 0.538)没有显着差异。当按性别对MS患者进行分层时,在等位基因或基因型分布中未观察到统计学上的显着差异。最后,没有迹象表明ACE I / D基因型对疾病进程或严重程度有影响。结论:ACE I / D多态性不是发展MS的危险因素,也不会导致该波斯尼亚和黑塞哥维那人口的疾病严重程度。

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  • 来源
    《Genetic Testing》 |2011年第11期|p.835-838|共4页
  • 作者单位

    Department of Neurology, School of Medicine, University of Mostar, Mostar, Bosnia and Herzegovina;

    Institute of Medical Genetics, UMC, Ljubljana, Slovenia;

    Institute of Medical Genetics, UMC, Ljubljana, Slovenia;

    Department of Neurology, School of Medicine, University of Tuzla, Tuzla, Bosnia and Herzegovina;

    Department of Neurology, School of Medicine, University of Tuzla, Tuzla, Bosnia and Herzegovina;

    Department of Neurology, School of Medicine, University of Tuzla, Tuzla, Bosnia and Herzegovina;

    Department of Biology and Medical Genetics, and Postgraduate Studies, School of Medicine, University of Rijeka, Rijeka, Croatia;

    Department of Biology and Medical Genetics School of Medicine University of Rijeka Brace Branchetta 20 51000 Rijeka Croatia;

    Department of Biology and Medical Genetics, and Postgraduate Studies, School of Medicine, University of Rijeka, Rijeka, Croatia;

    Department of Biology and Medical Genetics, and Postgraduate Studies, School of Medicine, University of Rijeka, Rijeka, Croatia,Department of Biology and Medical Genetics School of Medicine University of Rijeka Brace Branchetta 20 51000 Rijeka Croatia;

  • 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
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  • 入库时间 2022-08-17 13:19:27

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