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Prevention and control of phosphate retention/hyperphosphatemia in CKD-MBD: what is normal, when to start, and how to treat?慢性肾脏病矿物质和骨异常(CKD-MBD)中磷潴留/高磷血症的预防和控制:何为正常、何时开始以及如何治疗?
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本文引用的文献

1
KDIGO clinical practice guideline for the diagnosis, evaluation, prevention, and treatment of Chronic Kidney Disease-Mineral and Bone Disorder (CKD-MBD).改善全球肾脏病预后组织(KDIGO)慢性肾脏病-矿物质和骨异常(CKD-MBD)诊断、评估、预防及治疗临床实践指南。
Kidney Int Suppl. 2009 Aug(113):S1-130. doi: 10.1038/ki.2009.188.
2
The five most commonly used intact parathyroid hormone assays are useful for screening but not for diagnosing bone turnover abnormalities in CKD-5 patients.五种最常用的全段甲状旁腺激素检测方法对慢性肾脏病5期患者的骨转换异常筛查有用,但对诊断无用。
Clin Nephrol. 2009 Jul;72(1):5-14. doi: 10.5414/cnp72005.
3
Femoral bone mineral density reflects histologically determined cortical bone volume in hemodialysis patients.血液透析患者的股骨骨密度反映了组织学确定的皮质骨体积。
Osteoporos Int. 2010 Apr;21(4):619-25. doi: 10.1007/s00198-009-0988-9. Epub 2009 Jun 25.
4
Critical issues of PTH assays in CKD.慢性肾脏病中甲状旁腺激素检测的关键问题
Bone. 2009 Apr;44(4):666-70. doi: 10.1016/j.bone.2008.12.016. Epub 2008 Dec 30.
5
Low bone volume--a risk factor for coronary calcifications in hemodialysis patients.低骨量——血液透析患者冠状动脉钙化的一个危险因素。
Clin J Am Soc Nephrol. 2009 Feb;4(2):450-5. doi: 10.2215/CJN.01870408. Epub 2009 Jan 21.
6
Expression of gremlin, a bone morphogenetic protein antagonist,is associated with vascular calcification in uraemia.骨形态发生蛋白拮抗剂gremlin的表达与尿毒症血管钙化有关。
Nephrol Dial Transplant. 2009 Apr;24(4):1121-9. doi: 10.1093/ndt/gfn611. Epub 2008 Nov 21.
7
Improvements in renal osteodystrophy in patients treated with lanthanum carbonate for two years.接受碳酸镧治疗两年的患者肾性骨营养不良有所改善。
Clin Nephrol. 2008 Oct;70(4):284-95.
8
Vascular calcifications, vertebral fractures and mortality in haemodialysis patients.血液透析患者的血管钙化、椎体骨折与死亡率
Nephrol Dial Transplant. 2009 Jan;24(1):239-46. doi: 10.1093/ndt/gfn466. Epub 2008 Aug 25.
9
Fibroblast growth factor 23 and mortality among patients undergoing hemodialysis.成纤维细胞生长因子23与接受血液透析患者的死亡率
N Engl J Med. 2008 Aug 7;359(6):584-92. doi: 10.1056/NEJMoa0706130.
10
Calcium-containing phosphate binders in dialysis patients with cardiovascular calcifications: should we CARE-2 avoid them?患有心血管钙化的透析患者中含钙的磷酸盐结合剂:我们是否应该在CARE-2研究中避免使用它们?
Nephrol Dial Transplant. 2008 Oct;23(10):3050-2. doi: 10.1093/ndt/gfn393. Epub 2008 Jul 14.

《新的肾脏疾病:改善全球预后(KDIGO)指南——专家对骨与血管钙化的临床关注》

The new kidney disease: improving global outcomes (KDIGO) guidelines - expert clinical focus on bone and vascular calcification.

作者信息

London G, Coyne D, Hruska K, Malluche H H, Martin K J

机构信息

Service de Néphrologie, Centre Hospitalier Manhès, Fleury Mérogis, France.

出版信息

Clin Nephrol. 2010 Dec;74(6):423-32.

PMID:21084045
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3770279/
Abstract

Chronic kidney disease-mineral and bone disorder (CKD-MBD) defines a triad of interrelated abnormalities of serum biochemistry, bone and the vasculature associated with chronic kidney disease (CKD). The new kidney disease: improving global outcomes (KDIGO) guidelines define the quality and depth of evidence supporting therapeutic intervention in CKD-MBD. They also highlight where patient management decisions lack a strong evidence base. Expert interpretation of the guidelines, along with informed opinion, where evidence is weak, may help develop effective clinical practice. The body of evidence linking poor bone health and reservoir function (the ability of bone to buffer calcium and phosphorus) with vascular calcification and cardiovascular outcomes is growing. Treating renal bone disease should be one of the primary aims of therapy for CKD. Evaluation of the biochemical parameters of CKD-MBD (primarily phosphorus, calcium, parathyroid hormone and vitamin D levels) as early as CKD Stage 3, and an assessment of bone status (by the best means available), should be used to guide treatment decisions. The adverse effects of high phosphorus intake relative to renal clearance (including stimulation of hyperparathyroidism) precede hyperphosphatemia, which presents late in CKD. Early reduction of phosphorus load may ameliorate these adverse effects. Evidence that calcium load may influence progression of vascular calcification with effects on mortality should also be considered when choosing the type and dose of phosphate binder to be used. The risks, benefits, and strength of evidence for various treatment options for the abnormalities of CKD-MBD are considered.

摘要

慢性肾脏病 - 矿物质和骨异常(CKD-MBD)定义了与慢性肾脏病(CKD)相关的血清生化、骨骼和血管系统相互关联的三联征异常。新的改善全球肾脏病预后组织(KDIGO)指南明确了支持CKD-MBD治疗干预的证据质量和深度。它们还突出了患者管理决策缺乏有力证据支持的方面。在证据不足时,对指南的专业解读以及基于充分信息的观点,可能有助于制定有效的临床实践。将骨骼健康不佳和储备功能(骨骼缓冲钙和磷的能力)与血管钙化及心血管结局联系起来的证据越来越多。治疗肾性骨病应是CKD治疗的主要目标之一。早在CKD 3期就应对CKD-MBD的生化参数(主要是磷、钙、甲状旁腺激素和维生素D水平)进行评估,并采用现有最佳方法评估骨骼状况,以指导治疗决策。相对于肾脏清除率而言,高磷摄入的不良影响(包括刺激甲状旁腺功能亢进)在高磷血症之前就已出现,而高磷血症在CKD后期才出现。早期降低磷负荷可能改善这些不良影响。在选择使用的磷结合剂类型和剂量时,还应考虑钙负荷可能影响血管钙化进展并影响死亡率的证据。考虑了针对CKD-MBD异常的各种治疗选择的风险、益处和证据强度。