血清FGF-23和Klotho蛋白水平与尿毒症患者骨密度的相关性研究
Correlation between serum FGF-23 and Klotho protein levels and bone mineral density in uremic patients
  
DOI:10.3969/j.issn.1006.7108.2019.09.009
中文关键词:  血液透析  骨密度  成纤维细胞生长因子23  Klotho蛋白
英文关键词:hemodialysis  bone mineral density  fibroblast growth factor 23  Klotho protein
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作者单位
陶永亮* 儋州市人民医院海南 儋州 571700 
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中文摘要:
      目的 分析尿毒症维持性血液透析(MHD)患者血清成纤维细胞生长因子23(FGF-23)和Klotho蛋白水平与骨密度(BMD)的相关性。方法 2017年1月至2018年6月,我院收治了130例MHD患者。双能X线骨密度仪用于检查MHD患者股骨颈和腰椎的BMD。将患者分为3组:正常骨量组,骨量减少组和骨质疏松组。进行ELISA以测量血清FGF-23,Klotho蛋白和1,25(OH)2D3水平。还测量了其他参数,包括钙(Ca),磷(P)和甲状旁腺激素。结果 130例MHD患者中,49.60%的患者合并骨质疏松症,32.80%的患者出现骨量减少。骨质疏松症组血清FGF-23水平最高。然而,根据BMD分组,3组血清FGF-23水平差异无统计学意义 (P>0.05)。Spearman相关分析还指出血清FGF-23水平与BMD之间缺乏相关性。骨质疏松组血清Klotho蛋白水平明显低于正常骨量组和骨量减少组(P<0.05)。血清Klotho蛋白水平与股骨颈和腰椎的BMD和T值呈正相关。多元线性回归分析结果显示,血清Klotho蛋白水平是影响MHD患者BMD的主要因素之一。结论 血清FGF-23水平与MHD患者BMD变化无关,而血清Klotho蛋白水平与BMD变化密切相关。
英文摘要:
      Objective To analyze the correlation between serum fibroblast growth factor 23 (FGF-23) and Klotho protein levels and bone mineral density (BMD) in uremia patients with maintenance hemodialysis (MHD). Methods From January 2017 to June 2018, 130 MHD patients in our hospital were enrolled. Dual-energy X-ray absorptiometry was used to examine BMD of the femoral neck and lumbar spine in MHD patients. The patients were divided into three groups, normal bone mass group, osteopenia group, and osteoporosis group. Levels of serum FGF-23, Klotho protein, and 1,25(OH)2VitD3 were measured with ELISA method. Other parameters, including calcium (Ca), phosphorus (P), and parathyroid hormone, were also measured. Results Of the 130 patients with MHD, 49.60% had osteoporosis and 32.80% had osteopenia. The serum FGF-23 level was highest in the osteoporosis group. However, there was no significant difference in serum FGF-23 levels among the three groups divided by BMD (P>0.05). Spearman’s correlation analysis indicated that there was no correlation between serum FGF-23 levels and BMD. Among the three groups, there were significant differences in serum Klotho protein levels and BMD (P< 0.05). Serum Klotho protein levels in the osteoporosis group were clearly lower than in the normal bone mass group and osteopenia group (P<0.05). There was a positive correlation between serum Klotho protein levels and BMD and T values of the femoral neck and lumbar spine. The results of a multiple linear regression analysis revealed that the serum Klotho protein level was one of the main factors affecting BMD in MHD patients. Conclusion The serum level of FGF-23 is not correlated with a change in BMD in MHD patients, whereas the serum Klotho protein level is associated with BMD.
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