3-hydroxyanthranilic acid is independently associated with monocyte chemoattractant protein-1 (CCL2) and macrophage inflammatory protein-1β (CCL4) in patients with chronic kidney disease

被引:19
作者
Pawlak, Krystyna [1 ]
Kowalewska, Anna [1 ]
Mysliwiec, Michal [2 ]
Pawlak, Dariusz [1 ,3 ]
机构
[1] Med Univ, Dept Monitored Pharrnacotherapy, PL-15089 Bialystok, Poland
[2] Med Univ, Dept Nephrol & Clin Transplantat, PL-15089 Bialystok, Poland
[3] Univ Warmia & Mazury Olsztyn, Dept Pharmacol & Toxicol, Fac Med Sci, Olsztyn, Poland
关键词
Anthranilic acid; 3-hydrohyanthranilic acid; CC-chemokines; Chronic renal disease; BETA-CHEMOKINE LEVELS; CAROTID ATHEROSCLEROSIS; TRYPTOPHAN-METABOLITES; CARDIOVASCULAR-DISEASE; ENDOTHELIAL-CELLS; OXIDATIVE STRESS; INTERFERON-GAMMA; RENAL-FAILURE; KYNURENINE; EXPRESSION;
D O I
10.1016/j.clinbiochem.2010.06.008
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: CC-chemokines and kynurenine pathway (KP) metabolites are associated with accelerated atherosclerosis in chronic kidney disease (CKD) patients. Design and methods: We evaluate the plasma levels of anthranilic acid (AA), 3-hydroxyanthranilic acid (3-HAA) and their possible relationship with CC-chemokines, Cu/Zn superoxide dismutase (Cu/Zn SOD) as the marker of oxidative status and high sensitivity C-reactive protein (hsCRP) as an index of inflammation in the population of 48 CKD patients. Results: Compared with controls, CKD patients showed a significant increase in plasma concentrations of CCL2, CCL4, AA, 3-HAA, Cu/Zn SOD and hsCRP. Multiple stepwise regression analysis identified inflammation, renal function and 3-HAA levels as the independent variables significantly associated with increased CCL2; whereas age, 3-HAA and renal function as independent variables associated with CCL4. Conclusions: These results suggest a relationship between CC-chemokine system and KP activation, which may represent one of the mechanisms involved in the accelerated atherosclerosis in CKD population. (C) 2010 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1101 / 1106
页数:6
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