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骨转换的循环标志物。

Circulating markers of bone turnover.

机构信息

Department of Nephrology and Institute of Cardiovascular Research, VU University Medical Center, De Boelelaan 1117, 1081 HV, Amsterdam, The Netherlands.

Department of Cardiology, RWTH University Hospital Aachen, Aachen, Germany.

出版信息

J Nephrol. 2017 Oct;30(5):663-670. doi: 10.1007/s40620-017-0408-8. Epub 2017 May 13.

Abstract

Renal osteodystrophy is a feature of chronic kidney disease (CKD), with increasing prevalence as CKD progresses. This bone disease is responsible for major morbidity, including fractures, and a deterioration in the quality of life and its sequelae. Circulating biomarkers of renal osteodystrophy typically indicate bone turnover, but not other features of bone, like bone volume, mineralization, quality or strength. Bone turnover can be considered to be primarily a reflection of bone cell activity, in particular that of osteoblasts and osteoclasts. Since current treatments for bone disease usually target cellular activity, biomarkers are considered to be able to contribute to the decision-making for treatment and its follow-up. In CKD, one has to consider the impact of a diminished clearance of biomarkers or their altered metabolism, both potentially limiting its clinical use. Here, several aspects of the most frequently used biomarkers of bone turnover are reviewed, with an emphasis on the specific situation represented by CKD. This review is based on the overview lecture at the symposium held in Amsterdam, September 23, 2016: "The Bone In CKD", organized by the CKD-MBD working group of ERA-EDTA.

摘要

肾性骨营养不良是慢性肾脏病(CKD)的一个特征,随着 CKD 的进展,其患病率逐渐增加。这种骨病会导致严重的发病率,包括骨折,以及生活质量的恶化及其后果。肾性骨营养不良的循环生物标志物通常表明骨转换,但不包括其他骨特征,如骨量、矿化、质量或强度。骨转换可被认为主要反映骨细胞的活性,特别是成骨细胞和破骨细胞的活性。由于目前针对骨病的治疗通常针对细胞活性,因此生物标志物被认为能够为治疗及其随访的决策提供帮助。在 CKD 中,人们必须考虑生物标志物清除减少或其代谢改变的影响,这两者都可能限制其临床应用。本文重点介绍 CKD 所代表的特殊情况,对骨转换最常用的生物标志物的几个方面进行了综述。这篇综述是基于 2016 年 9 月 23 日在阿姆斯特丹举行的“CKD 中的骨”研讨会的概述讲座编写的,该研讨会由 ERA-EDTA 的 CKD-MBD 工作组组织。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/258d/5628199/72986014f459/40620_2017_408_Fig1_HTML.jpg

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