Division of Nephrology and Hypertension, Department of Medicine, Beth Israel Medical Center, New York, NY 10003, USA.
Blood Purif. 2010;29(3):293-9. doi: 10.1159/000276666. Epub 2010 Jan 21.
Dual X-ray absorptiometry is the standard diagnostic modality for identification of low bone mineral density, a finding which is in the general population usually indicative of osteopenia or osteoporosis. However, chronic kidney disease (CKD) patients diagnosed with osteopenia or osteoporosis may in actual fact have renal osteodystrophy with high or low bone turnover. While bisphosphonates are currently prescribed for the prevention of fractures in osteoporosis and high-risk osteopenic patients, the clinical utility of bisphosphonate therapy in CKD has not been established. Furthermore, bisphosphonates accumulate in bone, inhibit osteoclasts, and may cause or exacerbate low-turnover (adynamic) bone disease - particularly in patients presenting with low parathyroid hormone (PTH) levels or receiving treatment for secondary hyperparathyroidism. Bone biopsy with non-decalcified histopathology remains the gold standard for the identification and evaluation of bone disorders, including osteoporosis and renal osteodystrophy. Thirteen CKD patients (stage II-IV), referred to our clinic over a 12-month period, were identified as having taken bisphosphonates from 4 to >60 months after a diagnosis of osteopenia or osteoporosis. All patients underwent biopsies of trabecular bone from the iliac crest following oral administration of time-separated doses of doxycycline and tetracycline. Bone pathology was assessed after processing for mineralized histology. For all patients, clinical data collection included assessment of likely causes of kidney disease, MDRD glomerular filtration rate, calcium-phosphate product, intact PTH level, alkaline phosphatase, and bisphosphonate exposure. All 13 patients were diagnosed with adynamic bone on biopsy evaluation. Eleven biopsies revealed decreased cancellous bone mass; 8 showed decreased osteoid surface; 8 disclosed decreased osteoid thickness, and all 13 demonstrated low or low-normal osteoclast/osteoblast interface. Assessment of dynamic bone formation demonstrated decreased or absent single- or double-labeled osteoid in all 13 bone specimens. Based on these observations, the use of bisphosphonates in CKD cannot be recommended.
双能 X 线吸收法是诊断低骨密度的标准方法,而低骨密度通常提示骨质疏松症或骨量减少。然而,在患有骨质疏松症或骨量减少的慢性肾脏病 (CKD) 患者中,实际上可能存在高或低骨转换的肾性骨营养不良。虽然双膦酸盐目前被用于预防骨质疏松症和高危骨量减少患者的骨折,但双膦酸盐治疗 CKD 的临床效果尚未确定。此外,双膦酸盐在骨骼中蓄积,抑制破骨细胞,并可能导致或加重低转换(无动力)骨病——特别是在甲状旁腺激素 (PTH) 水平较低或正在接受继发性甲状旁腺功能亢进治疗的患者中。非脱钙组织病理学骨活检仍然是识别和评估骨疾病(包括骨质疏松症和肾性骨营养不良)的金标准。在过去的 12 个月中,我们的诊所共发现 13 名 CKD 患者(II-IV 期)在被诊断为骨质疏松症或骨量减少后 4 至 >60 个月期间服用了双膦酸盐。所有患者在口服间隔剂量多西环素和四环素后,均接受了髂嵴小梁骨活检。在进行矿化组织学处理后评估骨病理学。对于所有患者,临床数据收集包括评估可能导致肾脏疾病的原因、MDRD 肾小球滤过率、钙磷乘积、完整 PTH 水平、碱性磷酸酶和双膦酸盐暴露情况。所有 13 名患者的活检评估均诊断为无动力性骨病。11 个活检显示松质骨量减少;8 个显示类骨质表面减少;8 个显示类骨质厚度减少,所有 13 个都显示低或正常低值的破骨细胞/成骨细胞界面。所有 13 个骨标本的动态骨形成评估均显示单或双标记类骨质减少或缺失。基于这些观察结果,不能推荐在 CKD 中使用双膦酸盐。
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