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非透析慢性肾脏病继发甲状旁腺功能亢进症的治疗:2022 年评价。

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

机构信息

Department of General Internal Medicine and Nephrology, Robert-Bosch-Krankenhaus, Stuttgart, Germany.

Nephrology Department, University Hospital Germans Trias i Pujol, Badalona, Catalonia, Spain.

出版信息

Nephrol Dial Transplant. 2023 May 31;38(6):1397-1404. doi: 10.1093/ndt/gfac236.

DOI:10.1093/ndt/gfac236
PMID:35977397
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10229290/
Abstract

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.

摘要

未透析慢性肾脏病(ND-CKD)患者继发性甲状旁腺功能亢进症(SHPT)的情况可能最好用 2017 年改善全球肾脏病预后组织慢性肾脏病-矿物质和骨异常更新指南 4.2.1 来描述,该指南指出这些阶段的最佳甲状旁腺激素水平尚不清楚。此外,由于活性维生素 D 类似物在早期 CKD 阶段和中度 SHPT 表型中的常规使用可能会增加高钙血症和高磷血症的风险,因此建议对此类药物的使用持谨慎态度。然而,仍然存在大量的临床需求,需要预防甲状旁腺自主性的发展,及其相关的骨骼和血管损伤的后果,包括骨折风险和心血管事件。因此,我们现在试图审查当前基于指南的和临床实践管理 ND-CKD 中的 SHPT,包括它们的优缺点,以尊重钙和磷酸盐稳态的个体化方法。我们进一步评论了新型的缓释型骨化三醇(ERC),因为它是一种新的治疗选择,现在也可在欧洲使用,以及对更晚期 CKD 阶段中维生素 D 饱和度的潜在新认识。然而,除非进行具有强大的、有意义的终点的随机对照试验,否则毫无疑问仍会存在知识空白。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4e3/10229290/001426003f6e/gfac236fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4e3/10229290/001426003f6e/gfac236fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4e3/10229290/001426003f6e/gfac236fig1.jpg

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