Endostatin, Cathepsin S, and Cathepsin L, and Their Association with Inflammatory Markers and Mortality in Patients Undergoing Hemodialysis

被引:15
|
作者
Carlsson, Axel C. [1 ,2 ]
Carrero, Juan-Jesus [3 ]
Stenvinkel, Peter [3 ]
Bottai, Matteo [4 ]
Barany, Peter [3 ]
Larsson, Anders [5 ]
Arnlov, Johan [2 ,6 ]
机构
[1] Karolinska Inst, Dept Neurobiol Care Sci & Soc, Div Family Med, Huddinge, Sweden
[2] Uppsala Univ, Dept Med Sci, S-75185 Uppsala, Sweden
[3] Karolinska Inst, Dept Renal Med Clin Sci Intervent & Technol, Stockholm, Sweden
[4] Karolinska Inst, Inst Environm Med, Div Biostat, S-10401 Stockholm, Sweden
[5] Uppsala Univ, Dept Med Sci, S-75185 Uppsala, Sweden
[6] Dalarna Univ, Sch Hlth & Social Studies, Falun, Sweden
基金
瑞典研究理事会;
关键词
Patients; TNF; Laplace regression; Mortality; Inflammation; CHRONIC KIDNEY-DISEASE; RECOMBINANT HUMAN ENDOSTATIN; COMMUNITY-BASED COHORTS; BETA-TRACE PROTEIN; TNF RECEPTORS 1; ATRIAL-FIBRILLATION; CYSTATIN-C; BETA(2)-MICROGLOBULIN; GENERATION; FIBROSIS;
D O I
10.1159/000381664
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Although both endostatin and cathepsins S have been associated with higher mortality, data in patients with end-stage renal disease (ESRD) are scarce. Methods: A longitudinal cohort study of 207 prevalent patients undergoing hemodialysis. Results: Cathepsins S and L were associated with soluble receptors for tumor necrosis factor (sTNFR1 and sTNFR2, rho between 0.28 and 0.43, p < 0.001 for all). Weaker or absent associations between endostatin, cathepsins S and L were seen with other inflammatory biomarkers, that is, CRP, interleukin 6, pentraxin 3, and TNF. In Cox and Laplace regression models adjusted for age, sex, dialysis vintage, and diabetes: standard deviation increments of endostatin was associated with a lower mortality (hazard ratio 0.75, 95% confidence interval (CI) 0.57-0.98), and with 6.8 months longer median survival. Conclusions: The high levels of endostatin, cathepsins S and L, and their associations with sTNFR1 and sTNFR2 warrant further studies exploring mortality, and the angiogenic and inflammatory pathways in ESRD. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:259 / 265
页数:7
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