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糖尿病肾病的生物标志物。

Biomarkers of diabetic kidney disease.

机构信息

MRC Institute of Genetics & Molecular Medicine, The University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, EH4 2XU, UK.

Department of Paediatrics, University of Cambridge, Cambridge, UK.

出版信息

Diabetologia. 2018 May;61(5):996-1011. doi: 10.1007/s00125-018-4567-5. Epub 2018 Mar 8.

Abstract

Diabetic kidney disease (DKD) remains one of the leading causes of reduced lifespan in diabetes. The quest for both prognostic and surrogate endpoint biomarkers for advanced DKD and end-stage renal disease has received major investment and interest in recent years. However, at present no novel biomarkers are in routine use in the clinic or in trials. This review focuses on the current status of prognostic biomarkers. First, we emphasise that albuminuria and eGFR, with other routine clinical data, show at least modest prediction of future renal status if properly used. Indeed, a major limitation of many current biomarker studies is that they do not properly evaluate the marginal increase in prediction on top of these routinely available clinical data. Second, we emphasise that many of the candidate biomarkers for which there are numerous sporadic reports in the literature are tightly correlated with each other. Despite this, few studies have attempted to evaluate a wide range of biomarkers simultaneously to define the most useful among these correlated biomarkers. We also review the potential of high-dimensional panels of lipids, metabolites and proteins to advance the field, and point to some of the analytical and post-analytical challenges of taking initial studies using these and candidate approaches through to actual clinical biomarker use.

摘要

糖尿病肾病(DKD)仍然是糖尿病患者寿命缩短的主要原因之一。近年来,人们对用于晚期 DKD 和终末期肾病的预后和替代终点生物标志物的研究投入了大量的资金和关注。然而,目前尚无新型生物标志物在临床上或试验中常规使用。本文重点介绍了预后生物标志物的现状。首先,我们强调白蛋白尿和 eGFR 与其他常规临床数据结合使用,如果使用得当,至少可以对未来的肾脏状况进行适度预测。事实上,许多当前生物标志物研究的一个主要局限性是,它们没有正确评估在这些常规临床数据基础上的预测边际增加。其次,我们强调许多候选生物标志物在文献中有大量零星报道,它们彼此之间紧密相关。尽管如此,很少有研究试图同时评估广泛的生物标志物,以确定这些相关生物标志物中最有用的标志物。我们还回顾了利用多维脂质、代谢物和蛋白质组学来推进该领域的潜力,并指出了在实际的临床生物标志物应用中,使用这些方法和候选方法进行初步研究所面临的一些分析和分析后挑战。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b2a/6448994/4f4c15877f33/125_2018_4567_Fig1_HTML.jpg

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