机构地区:[1]Institute of Nephrology, Zhong Da Hospital, Southeast University, Nanjing, Jiangsu 210009, China
出 处:《Chinese Medical Journal》2008年第21期2157-2161,共5页中华医学杂志(英文版)
摘 要:Background Vascular access (VA) dysfunction is a major clinical complication in the hemodialysis population and has a direct effect on dialysis outcome. This study was conducted to explore the role of microinflammation in the VA dysfunction in maintenance hemodialysis patients. Methods Forty-seven patients (male 35 and female 12) receiving maintenance hemodialysis were included for this study. They were divided into three groups: group 1 (n=15), patients with initial hemodialysis and new arteriovenous fistula (AVF); group 2 (n=18), patients treated with hemodialysis for long term with well-functional VA; group 3 (n=14), maintenance hemodialysis patients with VA dysfunction. Biochemical parameters and serum tumor necrosis factor-α (TNF-α), interleukin 6 (IL-6) and monocyte chemoattractant protein-1 (MCP-1) were determined. High-sensitivity C-reactive protein (hs-CRP) was determined by latex-enhanced immuno-nephelometric method. Tissues of radial artery were taken from group 1 and group 3 for the histological study. Expression of CD68 and MCP-1 in the radial artery was determined by immunohistochemistry. Results Serum hs-CRP in group 3 was significantly higher than those in group 1 and group 2 ((7.40±2.42) mg/L vs (4.21±1.62) mg/L and (5.04±3.65) mg/L, P 〈0.01 and P 〈0.05, respectively). Serum TNF-α in group 3 was significantly higher than those in group 1 and group 2 ((64.03±9.29) pg/ml vs (54.69±12.39) pg/ml and (54.05±7.68) pg/ml, P 〈0.05 and P 〈0.01, respectively). Serum IL-6 in group 3 was also significantly higher than those in group 1 and group 2 ((70.09±14.53) pg/ml vs (56.43±10.11) pg/ml and (60.77±9.70) pg/ml, P 〈0.01 and P 〈0.05, respectively). Patients in group 3 had a thicker internal layer of vessels than in group 1 ((0.356±0.056) mm vs (0.111±0.021) mm, P 〈0.01). Expression of CD68 and MCP-1 in the fistula vessel walls in group 3 were much higher than those in group 1 (PBackground Vascular access (VA) dysfunction is a major clinical complication in the hemodialysis population and has a direct effect on dialysis outcome. This study was conducted to explore the role of microinflammation in the VA dysfunction in maintenance hemodialysis patients. Methods Forty-seven patients (male 35 and female 12) receiving maintenance hemodialysis were included for this study. They were divided into three groups: group 1 (n=15), patients with initial hemodialysis and new arteriovenous fistula (AVF); group 2 (n=18), patients treated with hemodialysis for long term with well-functional VA; group 3 (n=14), maintenance hemodialysis patients with VA dysfunction. Biochemical parameters and serum tumor necrosis factor-α (TNF-α), interleukin 6 (IL-6) and monocyte chemoattractant protein-1 (MCP-1) were determined. High-sensitivity C-reactive protein (hs-CRP) was determined by latex-enhanced immuno-nephelometric method. Tissues of radial artery were taken from group 1 and group 3 for the histological study. Expression of CD68 and MCP-1 in the radial artery was determined by immunohistochemistry. Results Serum hs-CRP in group 3 was significantly higher than those in group 1 and group 2 ((7.40±2.42) mg/L vs (4.21±1.62) mg/L and (5.04±3.65) mg/L, P 〈0.01 and P 〈0.05, respectively). Serum TNF-α in group 3 was significantly higher than those in group 1 and group 2 ((64.03±9.29) pg/ml vs (54.69±12.39) pg/ml and (54.05±7.68) pg/ml, P 〈0.05 and P 〈0.01, respectively). Serum IL-6 in group 3 was also significantly higher than those in group 1 and group 2 ((70.09±14.53) pg/ml vs (56.43±10.11) pg/ml and (60.77±9.70) pg/ml, P 〈0.01 and P 〈0.05, respectively). Patients in group 3 had a thicker internal layer of vessels than in group 1 ((0.356±0.056) mm vs (0.111±0.021) mm, P 〈0.01). Expression of CD68 and MCP-1 in the fistula vessel walls in group 3 were much higher than those in group 1 (P
关 键 词:MICROINFLAMMATION UREMIA arteriovenous fistula DYSFUNCTION HEMODIALYSIS
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