VITAMIN D AND UROLITHIASIS IN CHILDREN

S. Yusupov, A. Shamsiev, J. Shamsiev, P. A. Pulotov
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Abstract

Background. Urolithiasis is currently one of the topical issues of contemporary urology and medicine in general. This is primarily due to the high prevalence of urolithiasis; according to several population studies it ranges from 3.5 to 9.6%. At the same time, there is a steady increase in its incidence. Therefore, the matter of urolithiasis is one of the most urgent in present-day medicine. Objectives. The aim of the research was to study the content of a polymorphic genetic marker of the vitamin D receptor gene related to development and relapse of urolithiasis in children. Methods. The content of a polymorphic genetic marker of the vitamin D receptor gene related to development and relapse of urolithiasis in 100 children was investigated. Results. The results of the study prove that the vitamin D receptor gene assists in revealing disorders that promote urolithiasis development. Conclusion. Comparative analysis of the frequency of distribution of Fok1 genotypes of the vitamin D receptor gene polymorphism showed that statistical significance of the association (p=0.02) of f allele according to the dominant inheritance model (total Ff+ff genotypes) was established in the group of patients with urolithiasis compare to the corresponding indicator of the control group (63%).
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维生素D与儿童尿石症
背景泌尿系结石是当代泌尿外科和医学的一个热点问题。这主要是由于尿石症的高患病率;根据几项人口研究,它的发病率在3.5%到9.6%之间。与此同时,它的发生率稳步上升。因此,尿石症是当今医学上最紧迫的问题之一。目标。本研究的目的是研究与儿童尿石症发展和复发相关的维生素D受体基因多态性遗传标记的含量。方法。研究了100名儿童尿石症发生和复发相关的维生素D受体基因多态性遗传标记的含量。后果研究结果证明,维生素D受体基因有助于揭示促进尿石症发展的疾病。结论对维生素D受体基因多态性的Fok1基因型分布频率的比较分析表明,根据显性遗传模型(总Ff+Ff基因型),与对照组的相应指标(63%)相比,尿路结石患者组中f等位基因的相关性(p=0.02)具有统计学意义。
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发文量
14
审稿时长
36 weeks
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