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Biomarkers of Diabetic Nephropathy, the Present and the Future

机译:糖尿病肾病的生物标志物,现在和将来

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Diabetic nephropathy (DN) is a leading cause of end-stage renal disease. Searching for the perfect biomarker ofnDN has become the holy grail of nephrology since the burden of this disease is untenable. The only feasible way to tacklenthis health care crisis is by prevention and treatment in a mechanistically rational approach. Therefore, the discovery of anspecific, reliable diagnostic and prognostic biomarker for DN is imperative. Part of the difficulty in finding such a markernis the complex pathogenesis of DN; it is clearly multifactorial and involves multiple genes, proteins, metabolic pathways,nand environmental factors. In this review, we will discuss the latest findings in the use of genetic, protein, and metabolicnmarkers of DN. Particular attention will be paid to the urinary biomarker as a noninvasive method to detect either morphologicalnor biochemical changes in DN. Urinary protein and mRNA studies have focused on either the glomerularn(podocyte-specific) or tubular components (matrix or injury-related) of the nephron. The virtues and pitfalls of using thenpodocyte as a biomarker will be discussed. The systems biology approach of biomarker discovery in the studies of genomics,ntranscriptomics, proteomics, and metabolomics will be explored. Despite significant numbers of new biomarkers described,nmost studies are limited by either their small sample size or their cross-sectional nature, so that the ability to predictnfuture and severity of DN is lacking. In order to successfully search for the ideal, validated biomarker, we need tonconduct large, prospective, multi-center trials enlisting both Type 1 and Type II diabetic patients with and without nephropathynfor at least two decades
机译:糖尿病肾病(DN)是终末期肾脏疾病的主要原因。由于这种疾病的负担难以维持,因此寻找完美的nDN生物标志物已成为肾脏病的圣杯。解决这一医疗危机的唯一可行方法是采用机械合理的方法进行预防和治疗。因此,迫切需要发现一种特异性,可靠的DN诊断和预后生物标志物。寻找此类标志物的部分困难在于DN的复杂发病机制;它显然是多因素的,涉及多个基因,蛋白质,代谢途径,环境因素。在这篇综述中,我们将讨论DN的遗传,蛋白质和代谢标记物使用的最新发现。尿液生物标志物将作为一种非侵入性方法特别注意,以检测DN的形态学或生化变化。尿蛋白和mRNA的研究集中于肾小球的肾小球(足细胞特异性)或肾小管成分(基质或损伤相关)。将讨论使用足细胞作为生物标志物的优点和陷阱。将探索基因组学,转录组学,蛋白质组学和代谢组学研究中生物标志物发现的系统生物学方法。尽管描述了许多新的生物标志物,但大多数研究都受到样本量小或横截面性质的限制,因此缺乏预测DN未来和严重程度的能力。为了成功地寻找理想的,经过验证的生物标志物,我们需要进行至少20年的大型,前瞻性,多中心试验,包括患有和不患有肾病的1型和II型糖尿病患者。

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