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作为一项指数级技术的肾脏疾病临床蛋白质组学:迈向颠覆性阶段。

Clinical proteomics in kidney disease as an exponential technology: heading towards the disruptive phase.

作者信息

Sanchez-Niño Maria Dolores, Sanz Ana B, Ramos Adrian M, Fernandez-Fernandez Beatriz, Ortiz Alberto

机构信息

IIS-Fundacion Jimenez Diaz, School of Medicine, Universidad Autonoma de Madrid, Madrid, Spain, Fundacion Renal Iñigo Alvarez de Toledo-IRSIN, Madrid, Spain and REDINREN, Madrid, Spain.

出版信息

Clin Kidney J. 2017 Apr;10(2):188-191. doi: 10.1093/ckj/sfx023. Epub 2017 Mar 31.

DOI:10.1093/ckj/sfx023
PMID:28396735
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5381206/
Abstract

Exponential technologies double in power or processing speed every year, whereas their cost halves. Deception and disruption are two key stages in the development of exponential technologies. Deception occurs when, after initial introduction, technologies are dismissed as irrelevant, while they continue to progress, perhaps not as fast or with so many immediate practical applications as initially thought. Twenty years after the first publications, clinical proteomics is still not available in most hospitals and some clinicians have felt deception at unfulfilled promises. However, there are indications that clinical proteomics may be entering the disruptive phase, where, once refined, technologies disrupt established industries or procedures. In this regard, recent manuscripts in illustrate how proteomics is entering the clinical realm, with applications ranging from the identification of amyloid proteins in the pathology lab, to a new generation of urinary biomarkers for chronic kidney disease (CKD) assessment and outcome prediction. Indeed, one such panel of urinary peptidomics biomarkers, CKD273, recently received a Food and Drug Administration letter of support, the first ever in the CKD field. In addition, a must-read resource providing information on kidney disease-related proteomics and systems biology databases and how to access and use them in clinical decision-making was also recently published in .

摘要

指数技术的性能或处理速度每年都会翻番,而其成本则减半。欺骗和颠覆是指数技术发展的两个关键阶段。欺骗发生在技术最初引入后被认为无关紧要却仍在持续发展的时候,也许其发展速度不如最初设想的那么快,或者没有那么多直接的实际应用。在首次发表二十年后,大多数医院仍未提供临床蛋白质组学服务,一些临床医生对未兑现的承诺感到受骗。然而,有迹象表明临床蛋白质组学可能正在进入颠覆阶段,一旦完善,这些技术将颠覆既定的行业或程序。在这方面,最近的手稿阐述了蛋白质组学如何进入临床领域,其应用范围从病理实验室中淀粉样蛋白的鉴定,到用于慢性肾脏病(CKD)评估和预后预测的新一代尿液生物标志物。事实上,一组这样的尿液肽组学生物标志物CKD273最近收到了美国食品药品监督管理局的支持函,这在CKD领域尚属首次。此外,最近还发表了一份必读资源,提供了与肾脏疾病相关的蛋白质组学和系统生物学数据库的信息,以及如何在临床决策中访问和使用这些数据库。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/5381206/0cd92ddd3c34/sfx023f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/5381206/8d9f39cf2b30/sfx023f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/5381206/0cd92ddd3c34/sfx023f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/5381206/8d9f39cf2b30/sfx023f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8160/5381206/0cd92ddd3c34/sfx023f2.jpg

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Clin Kidney J. 2017 Apr;10(2):192-201. doi: 10.1093/ckj/sfx002. Epub 2017 Mar 29.
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Mixed leukocyte cell-derived chemotaxin 2 and amyloid A renal amyloidosis in a Kazakh-German patient.一名哈萨克 - 德国患者中的混合白细胞来源趋化因子2与淀粉样蛋白A肾淀粉样变性
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Albuminuria, Forgotten No More: Underlining the Emerging Role in CardioRenal Crosstalk.蛋白尿,不再被遗忘:突显其在心脏-肾脏相互作用中的新作用
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CKD Urine Metabolomics: Modern Concepts and Approaches.慢性肾脏病尿液代谢组学:现代概念与方法
Pathophysiology. 2023 Sep 29;30(4):443-466. doi: 10.3390/pathophysiology30040033.
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Clin Kidney J. 2022 Sep 20;16(2):230-244. doi: 10.1093/ckj/sfac212. eCollection 2023 Feb.
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