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Treatment of secondary hyperparathyroidism in non-dialysis CKD: an appraisal 2022s

期刊

NEPHROLOGY DIALYSIS TRANSPLANTATION
卷 38, 期 6, 页码 1397-1404

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OXFORD UNIV PRESS
DOI: 10.1093/ndt/gfac236

关键词

chronic kidney disease; CKD-MBD; parathyroid hormone; secondary hyperparathyroidism

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This article reviews the management of secondary hyperparathyroidism in non-dialysis chronic kidney disease patients, discussing the strengths and weaknesses of guideline-based and clinical practice approaches, as well as the importance of individualized strategies and calcium-phosphate homeostasis. Additionally, it introduces a new treatment option and a potentially novel understanding of vitamin D saturation in advanced stages of chronic kidney disease.
The situation of secondary hyperparathyroidism (SHPT) in chronic kidney disease patients not on dialysis (ND-CKD) is probably best characterised by the Kidney Disease: Improving Global Outcomes Chronic Kidney Disease-Mineral and Bone Disorder Update 2017 guideline 4.2.1 stating that the optimal parathyroid hormone levels are not known in these stages. Furthermore, new caution became recommended with regard to the routine use of active vitamin D analogues in early CKD stages and moderate SHPT phenotypes, due to their potential risks for hypercalcaemia and hyperphosphataemia aggravation. Nevertheless, there is still a substantial clinical need to prevent the development of parathyroid gland autonomy, with its associated consequences of bone and vascular damage, including fracture risks and cardiovascular events. Therefore we now attempt to review the current guideline-based and clinical practice management of SHPT in ND-CKD, including their strengths and weaknesses, favouring individualised approaches respecting calcium and phosphate homeostasis. We further comment on extended-release calcifediol (ERC) as a new differential therapeutic option now also available in Europe and on a potentially novel understanding of a required vitamin D saturation in more advanced CKD stages. There is no doubt, however, that knowledge gaps will remain unless powerful randomised controlled trials with hard and meaningful endpoints are performed.

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