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[慢性肾脏病 - 矿物质与骨异常:病理生理学及指南]

[Chronic kidney disease - Mineral bone disorders: Physiopathology and guidelines].

作者信息

Lavainne F, Guillot P, Figueres L

机构信息

Association ECHO dialyse et néphrologie, Nantes, France.

Service de rhumatologie, CHU de Nantes, place Alexis-Ricordeau, Nantes, France.

出版信息

Rev Med Interne. 2022 Apr;43(4):225-232. doi: 10.1016/j.revmed.2022.01.009. Epub 2022 Feb 25.

DOI:10.1016/j.revmed.2022.01.009
PMID:35227526
Abstract

Chronic Kidney Disease (CKD) is associated with a strong impact on phosphocalcic homeostasis, due to the chronic reduction in glomerular filtration rate (GFR) (phosphate excretion decrease), the inhibition of calcitriol synthesis and dietary restrictions. CKD-Mineral and Bone Disorders (CKD-MBD) must be monitored in CKD patients with biological work-up associated with bone markers and bone density dual X-ray absorptiometry. Adapted diet (phosphate restriction, normalization of calcium intake) and medications (vitamin D, phosphate binders, calcimimetics) help to correct CKD-MBD. Serum parathormone must be kept between 2 to 9 times the usual values, to limit renal osteodystrophy and avoid tertiary hyperparathyroidism. CKD patients are also at risk of artery calcifications, which can significantly increase the morbidity and mortality of the affection. Bisphosphonates may be used after correction of biological abnormalities, in patients with estimated GFR above 30ml/min/1,73m. Even if transplantation aims to normalize kidney function, kidney transplant recipients remain at risk of CKD-MBD. Biology and bone density dual X-ray absorptiometry must be regularly assessed, especially in the few months following the transplantation. More studies are needed to know if treatments of CKD-MBD are well tolerated in severe CKD and if they are associated with a decrease of bone fracture and vascular calcifications.

摘要

慢性肾脏病(CKD)由于肾小球滤过率(GFR)长期降低(磷酸盐排泄减少)、骨化三醇合成受抑制以及饮食限制,对磷钙稳态有强烈影响。对于CKD患者,必须通过与骨标志物和骨密度双能X线吸收测定相关的生物学检查来监测CKD - 矿物质和骨代谢紊乱(CKD - MBD)。调整饮食(限制磷酸盐、使钙摄入量正常化)和药物治疗(维生素D、磷酸盐结合剂、拟钙剂)有助于纠正CKD - MBD。血清甲状旁腺激素必须保持在正常水平的2至9倍之间,以限制肾性骨营养不良并避免继发性甲状旁腺功能亢进。CKD患者还存在动脉钙化风险,这会显著增加疾病的发病率和死亡率。对于估算肾小球滤过率高于30ml/min/1.73m²的患者,在纠正生物学异常后可使用双膦酸盐。即使肾移植旨在使肾功能正常化,但肾移植受者仍有发生CKD - MBD的风险。必须定期评估生物学指标和骨密度双能X线吸收测定,尤其是在移植后的几个月内。还需要更多研究来了解CKD - MBD的治疗在重度CKD中是否耐受性良好,以及它们是否与骨折和血管钙化的减少相关。

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