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骨保护素与慢性血液透析患者的尿毒症性骨质疏松

Osteoprotegerin and uremic osteoporosis in chronic hemodialysis patients.

作者信息

Moldovan Diana, Rusu Crina, Potra Alina, Moldovan Ioan, Patiu Ioan Mihai, Gherman-Caprioara Mirela, Kacso Ina Maria

机构信息

Department of Nephrology, University of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.

Nephrology and Dialysis Clinic, Emergency County Hospital, "Mihai Manasia", 3-5 Clinicilor Street, Cluj-Napoca, Romania.

出版信息

Int Urol Nephrol. 2017 May;49(5):895-901. doi: 10.1007/s11255-017-1529-7. Epub 2017 Feb 4.

Abstract

INTRODUCTION

Osteoprotegerin (OPG) is a powerful inhibitor of osteoclast activity, and it plays an important role in bone metabolism. In hemodialysis (HD) patients, the relationship between OPG and bone mineral density (BMD) is important, but remains unclear yet. The study objective was to assess the OPG role related to uremic osteoporosis in HD patients.

METHODS

This cross-sectional study has been realized on a cohort of 63 chronic HD patients.

INCLUSION CRITERIA

elderly prevalent HD patients with an age over 55 years old.

EXCLUSION CRITERIA

previous bone disease or previous renal transplant; neoplasia; parathyroidectomy, hormone replacement therapy. The data regarding demographical and clinical characteristics, including treatments for mineral and cardiovascular complications, were recorded. Serum OPG and mineral markers levels were measured. BMD was assessed by calcaneus quantitative ultrasound; it measured broadband ultrasound attenuation, speed of sound (SOS) and stiffness index (STI).

RESULTS

The high OPG levels were associated with higher bone mineral density (OPG-SOS P = 0.003; R = 0.37; OPG-STI P = 0.03; R = 0.28). Malnutrition, anemia and advanced age correlated with bone demineralization. Males had higher bone density parameters than females. In patients treated with vitamin D (P = 0.005), the BMD was increased comparing to patients without these treatments.

CONCLUSIONS

OPG levels had directly correlated with bone mineral density parameters. Our study further confirms the critical role of OPG in the pathogenesis of uremic osteoporosis in ESRD. Whether the increased circulant OPG protect against bone loss in patients undergoing HD remains to be established.

摘要

引言

骨保护素(OPG)是破骨细胞活性的强效抑制剂,在骨代谢中起重要作用。在血液透析(HD)患者中,OPG与骨矿物质密度(BMD)之间的关系很重要,但仍不清楚。本研究的目的是评估OPG在HD患者尿毒症性骨质疏松症中的作用。

方法

本横断面研究纳入了63例慢性HD患者。

纳入标准

年龄超过55岁的老年HD患者。

排除标准

既往有骨病或肾移植史;肿瘤;甲状旁腺切除术,激素替代疗法。记录人口统计学和临床特征数据,包括矿物质和心血管并发症的治疗情况。检测血清OPG和矿物质标志物水平。通过跟骨定量超声评估BMD;测量宽带超声衰减、声速(SOS)和硬度指数(STI)。

结果

OPG水平升高与较高的骨矿物质密度相关(OPG-SOS P = 0.003;R = 0.37;OPG-STI P = 0.03;R = 0.28)。营养不良、贫血和高龄与骨质脱矿有关。男性的骨密度参数高于女性。接受维生素D治疗的患者(P = 0.005),其BMD较未接受这些治疗的患者有所增加。

结论

OPG水平与骨矿物质密度参数直接相关。我们的研究进一步证实了OPG在终末期肾病尿毒症性骨质疏松症发病机制中的关键作用。循环中OPG升高是否能预防HD患者的骨质流失仍有待确定。

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