[an error occurred while processing this directive]
临床研究

组织蛋白酶K 升高是维持性血液透析患者心血管疾病死亡的危险因素

  • 许品品 ,
  • 朱丹 ,
  • 姚希
展开
  • 1连云港市第一人民医院检验科

收稿日期: 2021-05-08

  修回日期: 2021-08-04

  网络出版日期: 2021-10-12

Elevated Cathepsin K is a Risk Factor for Cardiovascular Death in Maintenance Hemodialysis Patients

  • XU Pin-Pin ,
  • ZHU Dan ,
  • YAO Xi
Expand
  •  1Laboratory of the first people's Hospital of Lianyungang City, Jiangsu Province, Lianyungang 222061, China

Received date: 2021-05-08

  Revised date: 2021-08-04

  Online published: 2021-10-12

摘要

【摘要】目的探讨组织蛋白酶K 水平与维持性血液透析(maintenance hemodialysis,MHD)患者心血管疾病(cardiovascular disease,CVD)死亡的关系。方法回顾性选择2017 年1 月~2019 年12 月连云港市第一人民医院血液净化中心96 例MHD 患者作为研究对象,另选择同期体检中心96 例健康人群作为对照。采用电化学发光法检测血清组织蛋白酶K 水平,采用Spearson 相关分析血清组织蛋白酶K 水平与临床病理特征及实验室指标的相关性,CVD 死亡的危险因素采用Logistic 回归分析。结果MHD 组患者血清组织蛋白酶K 水平为(280.75 ± 36.84)ng/L,高于健康对照组的(112.95 ± 20.14)ng/L(t=39.158,P<0.001)。MHD 存活组患者血清组织蛋白酶K 水平为(224.56±38.95)ng/L,低于MHD 因CVD死亡组的(417.21±35.99)ng/L(t=23.273,P<0.001)。MHD 患者血清组织蛋白酶K 水平与糖尿病史、白细胞计数呈负相关(r=-0.324,P=0.011;r=-0.311,P=0.009),与甲状旁腺激素、碱性磷酸酶、C 反应蛋白呈正相关(r=0.411,P=0.002;r=0.487,P<0.001;r=0.418,P=0.002)。多因素Logistic 回归分析显示,低血红蛋白水平、高组织蛋白酶K 水平是影响MHD 患者CVD 死亡的危险因素(OR=1.125, 95% CI:1.014~1.944, P=0.041;OR=2.012, 95% CI:1.411~6.254,P=0.003)。结论MHD 患者以及CVD 死亡患者血清组织蛋白酶K 水平显著升高,组织蛋白酶K 是MHD患者CVD 死亡危险因素标志物。

本文引用格式

许品品 , 朱丹 , 姚希 . 组织蛋白酶K 升高是维持性血液透析患者心血管疾病死亡的危险因素[J]. 中国血液净化, 2021 , 20(10) : 661 -664 . DOI: 10.3969/j.issn.1671-4091.2021.10.004

Abstract

【Abstract】Objective To investigate the relationship between Cathepsin K level and cardiovascular disease (CVD) death in maintenance hemodialysis (MHD) patients. Methods From Jan 2017 to Dec 2019, 96 MHD patients in the blood purification center of Lianyungang first people's hospital were selected as the research objects (MHD group, n=96). Another 96 healthy people in the physical examination center were selected as the control group (healthy control group, n=96). The serum cathepsin K level was detected by electrochemiluminescence. The correlation between serum cathepsin K level and clinicopathological features and laboratory parameters was analyzed by Pearson correlation. The risk factors of CVD death were analyzed by logistic regression. Results The serum Cathepsin K level of MHD group was 280.75±36.84 ng/L, which was significantly higher than that in healthy control group (112.95±20.14 ng/L,t=39.158, P<0.001). The serum Cathepsin K level of MHD survival group was 224.56±38.95 ng/L, which was significantly lower than that in CVD death group (417.21±35.99ng/L, t=23.273, P<0.001). The serum Cathepsin K level was negatively correlated with diabetes and white blood cell count (r=-0.324, P=0.011; r=-0.311, P=0.009), and positively correlated with parathyroid hormone, alkaline phosphatase and C-reactive protein(r=0.411, P=0.002; r=0.487, P<0.001; r=0.418, P=0.002). Low hemoglobin level and high Cathepsin K level were independent risk factors of CVD death in MHD patients (OR= 1.125, 95% CI:1.014~1.944, P=0.041; OR=2.012, 95% CI:1.411~6.254, P=0.003). Conclusion The serum Cathepsin K level is significantly increased in MHD patients and CVD death patients, and Cathepsin K is a potential biomarker of CVD death in MHD patients.

参考文献

[1]Soomro QH, Charytan DM. Cardiovascular autonomic nervous system dysfunction in chronic kidney disease and end-stage kidney disease: disruption of the complementary forces[J]. Curr Opin Nephrol Hypertens, 2021, 30(2):198-207.
[2]Mcglinchey RP, Lacy SM, Walker RL, et al. Cathepsin K is a potent disaggregase of α-synuclein fibrils[J]. Biochem Biophys Res Commun, 2020, 529(4):1106-1111.
[3]Yue XL, Jiang HY, Xu Y, et al. Cathepsin K deficiency impaired ischemia-induced neovascularization in aged mice[J]. Stem Cells Int, 2020, 6938620.
[4]Koldkj?r SAS, Harsl?f T, Langdahl B. Treatment with zoledronic acid subsequent to odanacatib prevents bone loss in postmenopausal women with osteoporosis[J]. Osteoporos Int, 2019, 30(5):995-1002.
[5]袁琳, 类延娜, 李玉子, 等. 组织蛋白酶K、胱抑素C与冠心病及其危险因素的相关性[J]. 中国老年学, 2015, 35(23):6725-6727.
[6]Izumi Y,?Hayashi M,?Morimoto R, et al. Impact of circulating cathepsin K on the coronary calcification and the clinical outcome in chronic kidney disease patients[J]. Heart Vessels, 2016, 31(1):6-14.
[7]Binkley N, Orwoll E, Chapurlat R, et al. Randomized, controlled trial to assess the safety and efficacy of odanacatib in the treatment of men with osteoporosis[J]. Osteoporos Int, 2021, 32(1):173-184.
[8]Yuan XY, Ren Z, Wu Y, et al. Design, synthesis and biological evaluation of inhibitors of cathepsin K on dedifferentiated chondrocytes[J]. Bioorg Med Chem, 2019, 27(6):1034-1042.
[9]王丹, 王治洁. 血清β-胶原降解产物、组织蛋白酶K和骨保护素对绝经后骨质疏松患者诊断的研究[J]. 中国骨质疏松杂志, 2019, 25(9):1231-1235.
[10]Bolignano D, Greco M, Arcidiacono V, et al. Increased circulating Cathepsin-K levels reflect PTH control in chronic hemodialysis patients[J]. J Nephrol, 2021, 34(2):451-458
[11]Carrillo-López N, Panizo S, Alonso-Montes C, et al. Direct inhibition of osteoblastic Wnt pathway by fibroblast growth factor 23 contributes to bone loss in chronic kidney disease[J]. Kidney Int, 2016, 90(1):77-89.
[12]Hao L, Zhu GC, Lu Y, et al. Deficiency of cathepsin K prevents inflammation and bone erosion in rheumatoid arthritis and periodontitis and reveals its shared osteoimmune role[J]. FEBS Lett, 2015, 589(12):1331-1339.
[13]Bolignano D, Greco M, Arcidiacono V, et al. Cathepsin-K is a potential cardiovascular risk biomarker in prevalent hemodialysis patients[J]. Int Urol Nephrol, 2021, 53(1):171-175.
[14]赵宇, 方正旭, 李丽莎, 等. 组织蛋白酶K、脂蛋白相关磷脂酶A2、缺血修饰白蛋白以及和肽素等因子与冠心病的关系综述[J]. 中国医学创新, 2019, 16(16):169-172.
[15]曾淑敏, 谭华清, 唐湘宇, 等. 血清组织蛋白酶K及胱抑素C水平与急性冠脉综合征的关系[J]. 现代实用医学, 2020, 32(12):1461-1463.
[16]郑婧, 林燕珊, 张健, 等. 老年人血清组织蛋白酶K与冠心病的相关性研究[J]. 实用老年医学, 2019, 33(10):1000-1003.
[17]Izumi Y, Hayashi M, Morimoto R, et al, Impact of circulating cathepsin K on the coronary cal-
cification and the clinical outcome in chronic kidney disease patients[J]. Heart Vessels, 2016, 31(1):6-14.
文章导航

/

[an error occurred while processing this directive]