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Vitamin D Supplementation for Patients with Chronic Kidney Disease: A Systematic Review and Meta-analyses of Trials Investigating the Response to Supplementation and an Overview of Guidelines
Calcified Tissue International ( IF 4.2 ) Pub Date : 2021-04-25 , DOI: 10.1007/s00223-021-00844-1
Marilena Christodoulou 1 , Terence J Aspray 2 , Inez Schoenmakers 1, 3
Affiliation  

A large proportion of patients with chronic kidney disease (CKD) are vitamin D deficient (plasma 25-hydroxyvitamin D (25(OH)D) < 25 or 30 nmol/L per UK and US population guidelines) and this contributes to the development of CKD–mineral bone disease (CKD–MBD). Gaps in the evidence-base for the management of vitamin D status in relation to CKD–MBD are hindering the formulation of comprehensive guidelines. We conducted a systemic review of 22 RCTs with different forms of vitamin D or analogues with CKD–MBD related outcomes and meta-analyses for parathyroid hormone (PTH). We provide a comprehensive overview of current guidelines for the management of vitamin D status for pre-dialysis CKD patients. Vitamin D supplementation had an inconsistent effect on PTH concentrations and meta-analysis showed non- significant reduction (P = 0.08) whereas calcifediol, calcitriol and paricalcitol consistently reduced PTH. An increase in Fibroblast Growth Factor 23 (FGF23) with analogue administration was found in all 3 studies reporting FGF23, but was unaltered in 4 studies with vitamin D or calcifediol. Few RCTS reported markers of bone metabolism and variations in the range of markers prevented direct comparisons. Guidelines for CKD stages G1–G3a follow general population recommendations. For the correction of deficiency general or CKD-specific patient guidelines provide recommendations. Calcitriol or analogues administration is restricted to stages G3b–G5 and depends on patient characteristics. In conclusion, the effect of vitamin D supplementation in CKD patients was inconsistent between studies. Calcifediol and analogues consistently suppressed PTH, but the increase in FGF23 with calcitriol analogues warrants caution.



中文翻译:

慢性肾脏病患者的维生素 D 补充剂:对研究补充剂反应的试验的系统评价和荟萃分析和指南概述

大部分慢性肾病 (CKD) 患者缺乏维生素 D(血浆 25-羟基维生素 D (25(OH)D) < 25 或 30 nmol/L,根据英国和美国人口指南),这有助于发展CKD-矿物质骨病(CKD-MBD)。与 CKD-MBD 相关的维生素 D 状态管理证据基础的空白阻碍了综合指南的制定。我们对 22 项不同形式的维生素 D 或类似物与 CKD-MBD 相关结果的 RCT 进行了系统评价,并对甲状旁腺激素 (PTH) 进行了荟萃分析。我们全面概述了透析前 CKD 患者维生素 D 状态管理的当前指南。补充维生素 D 对 PTH 浓度的影响不一致,荟萃分析显示没有显着降低(P = 0.08) 而骨化二醇、骨化三醇和帕立骨化醇始终降低 PTH。在报告 FGF23 的所有 3 项研究中发现,使用类似物给药后成纤维细胞生长因子 23 (FGF23) 增加,但在使用维生素 D 或骨化二醇的 4 项研究中未改变。很少有 RCTS 报告骨代谢标志物,并且标志物范围的变化阻止了直接比较。G1-G3a 期 CKD 指南遵循一般人群的建议。为纠正缺陷一般或 CKD 特定患者指南提供建议。骨化三醇或类似物的给药仅限于 G3b-G5 期,并取决于患者的特征。总之,维生素 D 补充剂对 CKD 患者的影响在不同研究之间并不一致。骨化二醇和类似物始终抑制 PTH,

更新日期:2021-04-26
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