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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
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页码:259 / 265
页数:7
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