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慢性肾脏病保守治疗中磷及慢性肾脏病-矿物质和骨异常的其他方面

Phosphorus and other aspects of CKD-MBD in the conservative management of chronic kidney disease.

作者信息

Shah Anuja

机构信息

Los Angeles Biomedical Research Institute, Harbor-UCLA, Torrance, CA, USA -

出版信息

Panminerva Med. 2017 Jun;59(2):124-132. doi: 10.23736/S0031-0808.17.03302-X.

Abstract

As the prevalence of chronic kidney disease (CKD) increases and the population ages, there is an imperative to offer cost effective and patient specific therapeutic options for the management of advanced CKD. In cases where there is a desire to avoid or delay renal replacement therapy, conservative options need to be defined and strategies for delaying the need for renal replacement therapy should be offered. CKD-mineral bone disorders (MBD) refers to the constellation of disturbances in abnormal bone and soft tissue calcification along with abnormalities, in phosphorus, calcium, parathyroid hormone, vitamin D, and FGF-23. CKD-MBD is associated with morbidity and mortality in dialysis patients. Addressing CKD-MBD necessitated understanding phosphorus handling in the intestine and kidney and the ordered process of vascular calcification and uremic osteodystrophy. Decreasing dietary phosphorus intake and absorption is the mainstay of conservative management of CKD-MBD; pharmacologic therapy with binders, vitamin D analogues, and niacin may also be indicated. FGF-23 levels, parathyroid hormone levels, tubular reabsorption of phosphorus, and 24 hour urinary phosphorus can be tracked to trigger and evaluate these interventions. Further research is required to generate an ordered multifaceted approach to CKD-MBD.

摘要

随着慢性肾脏病(CKD)患病率的上升以及人口老龄化,为晚期CKD的管理提供具有成本效益且针对患者个体的治疗选择变得势在必行。在希望避免或延迟肾脏替代治疗的情况下,需要明确保守治疗方案,并应提供延迟肾脏替代治疗需求的策略。CKD-矿物质和骨异常(MBD)是指异常骨和软组织钙化紊乱以及磷、钙、甲状旁腺激素、维生素D和FGF-23异常的一组情况。CKD-MBD与透析患者的发病率和死亡率相关。解决CKD-MBD需要了解肠道和肾脏中的磷代谢以及血管钙化和尿毒症骨营养不良的有序过程。减少饮食中磷的摄入和吸收是CKD-MBD保守治疗的主要方法;也可能需要使用磷结合剂、维生素D类似物和烟酸进行药物治疗。可以追踪FGF-23水平、甲状旁腺激素水平、磷的肾小管重吸收以及24小时尿磷,以启动和评估这些干预措施。需要进一步研究以制定针对CKD-MBD的有序多方面方法。

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