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Genetic factors in the development and progression of chronic kidney disease

机译:慢性肾脏病发展和进程中的遗传因素

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The factors influencing the onset and progression of chronic kidney disease (CKD) are not completely known. It is believed that genetic factors may play a significant role. The article presents the results of population, family, and animal studies which indicate the participation of genetic factors in CKD development. The main strategies for identifying genes involved in CKD development (genome scan studies and candidate gene studies) are described. Polymorphisms of selected candidate genes for CKD are reviewed. Special attention is paid to studies concerning the genes of the renin-angiotensin-aldosteron system (angiotensin-converting enzyme and angiotensin II type 1 receptor genes), cytokine genes (IL-10, IL-4, IL-6, IL-1beta, TNF-alpha, TGF-beta1, MCP, RANTES), and the gene encoding methylenetetrahydrofolate reductase. The results of studies on the role of TGFB1 gene in kidney diseases are analyzed. The genetic basis of IgA nephropathy and kidney insufficiency progression in the course of the disease is shown. The results of genetic studies of CKD are inconclusive. The article underlines the importance of identifying the genetic background of CKD to individualize patient therapy.
机译:影响慢性肾脏病(CKD)发作和发展的因素尚不完全清楚。相信遗传因素可能起重要作用。本文介绍了人口,家庭和动物研究的结果,这些结果表明遗传因素参与了CKD的发展。描述了识别参与CKD发展的基因的主要策略(基因组扫描研究和候选基因研究)。审查了CKD的选定候选基因的多态性。特别注意有关肾素-血管紧张素-醛固酮系统的基因(血管紧张素转换酶和血管紧张素II 1型受体基因),细胞因子基因(IL-10,IL-4,IL-6,IL-1beta, TNF-α,TGF-β1,MCP,RANTES)和编码亚甲基四氢叶酸还原酶的基因。分析了TGFB1基因在肾脏疾病中的作用的研究结果。显示了在疾病过程中IgA肾病和肾功能不全进展的遗传基础。 CKD基因研究的结果尚无定论。这篇文章强调了识别CKD的遗传背景以个性化患者治疗的重要性。

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