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首页> 外文期刊>Journal of biomedical science. >Association of Genetic polymorphism of Emphasis Type="Italic"PPARγ-2, ACE, MTHFR, FABP-2 and FTO/Emphasis genes in risk prediction of type 2 diabetes mellitus
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Association of Genetic polymorphism of Emphasis Type="Italic"PPARγ-2, ACE, MTHFR, FABP-2 and FTO/Emphasis genes in risk prediction of type 2 diabetes mellitus

机译:PPARγ-2,ACE,MTHFR,FABP-2和FTO 基因的遗传多态性与2型糖尿病风险预测的关联

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Type 2 diabetes mellitus (T2DM) is a non-autoimmune, complex, heterogeneous and polygenic metabolic disease condition characterized by persistent elevated blood glucose levels (hyperglycemia). India as said to be the diabetic capital of the world is likely to experience the largest increase in T2DM and a greater number of diabetic individuals in the world by the year 2030. Identification of specific genetic variations in a particular ethnic group has a critical role in understanding the risk of developing T2DM in a much efficient way in future. These genetic variations include numerous types of polymorphisms among which single nucleotide polymorphisms (SNPs) is the most frequent. SNPs are basically located within the regulatory elements of several gene sequences. There are scores of genes interacting with various environmental factors affecting various pathways and sometimes even the whole signalling network that cause diseases like T2DM. This review discusses the biomarkers for early risk prediction of T2DM. Such predictions could be used in order to understand the pathogenesis of T2DM and to better diagnostics, treatment, and eventually prevention.
机译:2型糖尿病(T2DM)是一种非自体免疫,复杂,异质和多基因代谢疾病,其特征在于持续升高的血糖水平(高血糖症)。到2030年,印度被认为是世界糖尿病之都,其T2DM增幅可能最大,并且全世界的糖尿病患者人数也将增加。在特定种族群体中特定遗传变异的识别在了解将来以更有效的方式开发T2DM的风险。这些遗传变异包括多种类型的多态性,其中单核苷酸多态性(SNP)最常见。 SNP基本上位于几个基因序列的调控元件内。有数十种基因与各种环境因素相互作用,这些因素会影响各种途径,有时甚至会影响导致T2DM等疾病的整个信号网络。这篇综述讨论了T2DM早期风险预测的生物标志物。可以使用此类预测来了解T2DM的发病机理,并更好地进行诊断,治疗以及最终预防。

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