Where are we now? Emerging opportunities and challenges in the management of secondary hyperparathyroidism in patients with non-dialysis chronic kidney disease

医学 继发性甲状旁腺功能亢进 肾脏疾病 透析 肾病科 人口 甲状旁腺激素 维生素D与神经学 内科学 西那卡塞特 重症监护医学 甲状旁腺功能亢进 疾病 血液透析 终末期肾病 泌尿科 腹膜透析 甲状旁腺切除术 肾脏替代疗法 肾性骨营养不良 维生素D缺乏 高磷血症 拟钙质 内分泌学 环境卫生
作者
Markus Ketteler,Patrice M. Ambühl
出处
期刊:Journal of Nephrology [Springer Science+Business Media]
卷期号:34 (5): 1405-1418 被引量:11
标识
DOI:10.1007/s40620-021-01082-2
摘要

Rising levels of parathyroid hormone (PTH) are common in patients with chronic kidney disease (CKD) not on dialysis and are associated with an elevated risk of morbidity (including progression to dialysis) and mortality. However, there are several challenges for the clinical management of secondary hyperparathyroidism (SHPT) in this population. While no recognised target level for PTH currently exists, it is accepted that patients with non-dialysis CKD should receive early and regular monitoring of PTH from CKD stage G3a. However, studies indicate that adherence to monitoring recommendations in non-dialysis CKD may be suboptimal. SHPT is linked to vitamin D [25(OH)D] insufficiency in non-dialysis CKD, and correction of low 25(OH)D levels is a recognised management approach. A second challenge is that target 25(OH)D levels are unclear in this population, with recent evidence suggesting that the level of 25(OH)D above which suppression of PTH progressively diminishes may be considerably higher than that recommended for the general population. Few therapeutic agents are licensed for use in non-dialysis CKD patients with SHPT and optimal management remains controversial. Novel approaches include the development of calcifediol in an extended-release formulation, which has been shown to increase 25(OH)D gradually and provide a physiologically-regulated increase in 1,25(OH)2D that can reliably lower PTH in CKD stage G3-G4 without clinically meaningful increases in serum calcium and phosphate levels. Additional studies would be beneficial to assess the comparative effects of available treatments, and to more clearly elucidate the overall benefits of lowering PTH in non-dialysis CKD, particularly in terms of hard clinical outcomes.

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