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骨质疏松症与慢性肾脏病-矿物质和骨异常(CKD-MBD):回归基础

Osteoporosis and Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD): Back to Basics.

作者信息

Pazianas Michael, Miller Paul D

机构信息

Institute of Musculoskeletal Sciences, Oxford University, Oxford, United Kingdom.

University of Colorado Health Sciences Center, Denver, Colorado; Colorado Center for Bone Health, Lakewood, Colorado.

出版信息

Am J Kidney Dis. 2021 Oct;78(4):582-589. doi: 10.1053/j.ajkd.2020.12.024. Epub 2021 Mar 25.

Abstract

Osteoporosis is defined as a skeletal disorder of compromised bone strength predisposing those affected to an elevated risk of fracture. However, based on bone histology, osteoporosis is only part of a spectrum of skeletal complications that includes osteomalacia and the various forms of renal osteodystrophy of chronic kidney disease-mineral and bone disorder (CKD-MBD). In addition, the label "kidney-induced osteoporosis" has been proposed, even though the changes caused by CKD do not qualify as osteoporosis by the histological diagnosis. It is clear, therefore, that such terminology may not be helpful diagnostically or in making treatment decisions. A new label, "CKD-MBD/osteoporosis" could be a more appropriate term because it brings osteoporosis under the official label of CKD-MBD. Neither laboratory nor noninvasive diagnostic investigations can discriminate osteoporosis from the several forms of renal osteodystrophy. Transiliac crest bone biopsy can make the diagnosis of osteoporosis by exclusion of other kidney-associated bone diseases, but its availability is limited. Recently, a classification of metabolic bone diseases based on bone turnover, from low to high, together with mineralization and bone volume, has been proposed. Therapeutically, no antifracture treatments have been approved by the US Food and Drug Administration for patients with kidney-associated bone disease. Agents that suppress parathyroid hormone (vitamin D analogues and calcimimetics) are used to treat hyperparathyroid bone disease. Antiresorptive and osteoanabolic agents approved for osteoporosis are being used off-label to treat CKD stages 3b-5 in high-risk patients. It has now been suggested that intermittent administration of parathyroid hormone as early as CKD stage 2 could be an effective management strategy. If confirmed in clinical trials, it could mitigate the retention of phosphorus and subsequently the rise in fibroblast growth factor 23 and may be beneficial for coexisting osteoporosis.

摘要

骨质疏松症被定义为一种骨骼疾病,其骨强度受损,使受影响者骨折风险升高。然而,基于骨组织学,骨质疏松症只是一系列骨骼并发症的一部分,这些并发症包括骨软化症以及慢性肾脏病 - 矿物质和骨异常(CKD - MBD)的各种形式的肾性骨营养不良。此外,尽管CKD引起的变化根据组织学诊断不符合骨质疏松症的标准,但“肾性骨质疏松症”这一术语已被提出。因此,很明显,这样的术语在诊断或治疗决策方面可能并无帮助。一个新的术语“CKD - MBD/骨质疏松症”可能是一个更合适的术语,因为它将骨质疏松症纳入了CKD - MBD的官方范畴。无论是实验室检查还是非侵入性诊断检查,都无法区分骨质疏松症与几种形式的肾性骨营养不良。经髂嵴骨活检可以通过排除其他与肾脏相关的骨病来诊断骨质疏松症,但这种检查的可及性有限。最近,有人提出了一种基于骨转换(从低到高)以及矿化和骨量的代谢性骨病分类方法。在治疗方面,美国食品药品监督管理局尚未批准任何用于治疗与肾脏相关骨病患者的抗骨折治疗药物。抑制甲状旁腺激素的药物(维生素D类似物和拟钙剂)用于治疗甲状旁腺功能亢进性骨病。已批准用于骨质疏松症的抗吸收和促骨合成药物正在用于治疗高风险患者的CKD 3b - 5期。现在有人提出,早在CKD 2期就间歇性给予甲状旁腺激素可能是一种有效的管理策略。如果在临床试验中得到证实,它可以减轻磷的潴留,进而减轻成纤维细胞生长因子23的升高,并且可能对并存的骨质疏松症有益。

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