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老年慢性肾脏病患者的骨质疏松症

Osteoporosis in the elderly with chronic kidney disease.

作者信息

Ersoy F Fevzi

机构信息

Division of Nephrology, Department of Medicine, Akdeniz University Medical School, Duluphar Bulvari, Kampus, 07070 Antalya, Turkey.

出版信息

Int Urol Nephrol. 2007;39(1):321-31. doi: 10.1007/s11255-006-9109-2. Epub 2006 Nov 11.

Abstract

Considering the aging dialysis population of today, increasing our knowledge about the nature, diagnosis and the treatment of bone mineral density (BMD) problems in end-stage renal disease (ESRD) patients deserves more attention. Osteoporosis is basicly defined as a decrease in bone mass. Large epidemiological studies in general population have identified several risk factors for osteoporosis including advancing age, female gender, white race, decreased calcium intake, gastric acid suppression therapy, sedentary lifestyle, premature loss of gonadal function, decreased estrogen secretion, thin body habitus, decreased physical activity, cigarette smoking, alcohol abuse, excess glucocorticoid exposure, and possibly some genetic factors. Osteoporosis in ESRD patients is only a part of a wider spectrum of metabolic bone problems, namely uremic osteodystrophy. Therefore, its diagnosis, management and follow-up may differ from the general population and an individualization of diagnosis and definition for dialysis population may be necessary. However, standard diagnostic tools such as dual energy X-ray absorptiometry (DEXA) have been widely used for the assessment of bone mineral deficiency status in ESRD patients. Regardless of the methods, most of the studies are in concordance with a reduced BMD in HD and PD patients. Dialysis patients are known to be at increased risk for low-trauma fractures. Thinning of cortical bone, which is responsible for the largest contribution toward reduced bone mineral content in chronic renal failure results in increased fracture risk. In either normal population and dialysis patients, fracture risk is increased with age. But in dialysis patients, besides age, several other factors may also affect the degree of bone mineral deficiency, and age-BMD relationship may be blunted. Female sex, in hemodialysis patients is negatively associated with total hip BMD. While several studies have been unable to demonstrate any association between BMD and PTH levels, larger body size has been shown to have a significant positive effect on BMD in both hemodialysis and peritoneal dialysis patients. Although they have been used in small groups of chronic kidney disease (CKD) and ESRD patients, because of their potential nephrotoxicity and hypocalcemic effects, use of biphosphonates in renal patients is questionable. Currently, bone biopsy, in order to exclude adynamic bone disease is recommended before beginning treatment with bisphosphonates in chronic kidney disease and dialysis patients.

摘要

考虑到当今透析患者群体的老龄化,增进我们对终末期肾病(ESRD)患者骨矿物质密度(BMD)问题的本质、诊断及治疗的了解值得更多关注。骨质疏松症基本上被定义为骨量减少。针对普通人群的大型流行病学研究已确定了骨质疏松症的若干风险因素,包括年龄增长、女性、白种人、钙摄入量减少、胃酸抑制治疗、久坐不动的生活方式、性腺功能过早丧失、雌激素分泌减少、体型消瘦、身体活动减少、吸烟、酗酒、糖皮质激素暴露过多以及可能的一些遗传因素。ESRD患者的骨质疏松症只是更广泛的代谢性骨病谱(即尿毒症骨营养不良)的一部分。因此,其诊断、管理及随访可能与普通人群不同,对透析人群的诊断和定义进行个体化可能是必要的。然而,双能X线吸收法(DEXA)等标准诊断工具已被广泛用于评估ESRD患者的骨矿物质缺乏状况。无论采用何种方法,大多数研究都一致认为血液透析(HD)和腹膜透析(PD)患者的BMD降低。已知透析患者发生低创伤性骨折的风险增加。皮质骨变薄是慢性肾衰竭中导致骨矿物质含量降低的最大因素,会增加骨折风险。在正常人群和透析患者中,骨折风险均随年龄增加而升高。但在透析患者中,除年龄外,其他几个因素也可能影响骨矿物质缺乏的程度,且年龄与BMD的关系可能不明显。女性血液透析患者的全髋BMD呈负相关。虽然多项研究未能证明BMD与甲状旁腺激素(PTH)水平之间存在任何关联,但更大的体型已被证明对血液透析和腹膜透析患者的BMD有显著的积极影响。尽管双膦酸盐已在一小部分慢性肾脏病(CKD)和ESRD患者中使用,但由于其潜在的肾毒性和低钙血症作用,在肾病患者中使用双膦酸盐存在疑问。目前,对于慢性肾脏病和透析患者,在开始使用双膦酸盐治疗前,建议进行骨活检以排除动力缺失性骨病。

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