Pentraxin 3 Predicts Arteriovenous Fistula Functional Patency Loss and Mortality in Chronic Hemodialysis Patients

被引:3
作者
Tsai, Heng-Cheng [1 ]
Ou, Shuo-Ming [1 ,2 ]
Wu, Chih-Cheng [3 ,4 ,5 ]
Huang, Chin-Chou [2 ,6 ]
Hsieh, Jyh-Tong [1 ]
Tseng, Po-Yu [2 ,7 ]
Lee, Chiu-Yang [2 ,8 ]
Yang, Chih-Yu [1 ,2 ,9 ,10 ,11 ,12 ]
Tarng, Der-Cherng [1 ,2 ,10 ,11 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med, Div Nephrol, Taipei, Taiwan
[2] Natl Yang Ming Chiao Tung Univ, Fac Med, Sch Med, Taipei, Taiwan
[3] Natl Taiwan Univ Hosp, Cardiovasc Ctr, Hsinchu Branch, Hsinchu, Taiwan
[4] Natl Taiwan Univ, Coll Med, Taipei, Taiwan
[5] Natl Tsing Hua Univ, Inst Biomed Engn, Hsinchu, Taiwan
[6] Taipei Vet Gen Hosp, Dept Med, Div Cardiol, Taipei, Taiwan
[7] Taipei City Hosp, Dept Med, Div Nephrol, Heping Fuyou Branch, Taipei, Taiwan
[8] Taipei Vet Gen Hosp, Dept Surg, Div Cardiovasc Surg, Taipei, Taiwan
[9] Taipei Vet Gen Hosp, Dept Med, Div Clin Toxicol & Occupat Med, Taipei, Taiwan
[10] Natl Yang Ming Chiao Tung Univ, Inst Clin Med, Sch Med, Taipei, Taiwan
[11] Ctr Intelligent Drug Syst & Smart Biodevices IDS2, Hsinchu, Taiwan
[12] Natl Yang Ming Chiao Tung Univ, Stem Cell Res Ctr, Taipei, Taiwan
关键词
Hemodialysis vascular access; Endothelial dysfunction; Functional patency; Mortality; Pentraxin; 3; GELATINASE-ASSOCIATED LIPOCALIN; C-REACTIVE PROTEIN; VASCULAR ACCESS; MOLECULAR CHARACTERIZATION; CARDIOVASCULAR MORTALITY; ENDOTHELIAL DYSFUNCTION; ARTERY-DISEASE; ALL-CAUSE; INFLAMMATION; MARKER;
D O I
10.1159/000522049
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Viable vascular access is the lifeline for hemodialysis patients. In the nondialysis population, emerging evidence suggests that circulating pentraxin 3 (PTX3), neutrophil gelatinase-associated lipocalin (NGAL), and chitinase-3-like protein 1 (CHI3L1) are associated with cardiovascular inflammation and endothelial injury. However, predictive values of these three biomarkers on arteriovenous fistula (AVF) outcomes are unknown. Methods: This prospective observational cohort study enrolled 135 hemodialysis patients using AVF and then followed them for 3 years. Plasma levels of PTX3, NGAL, and CHI3L1 were measured. Patients were followed up prospectively for two clinical outcomes, including AVF functional patency loss and death. Cox proportional hazards regression models were used to analyze hazard ratios for the commencement of AVF functional patency loss and mortality. Results: Among 135 patients, the mean age was 66.0 +/- 15.7 years old and 48.1% were male. The plasma level of PTX3, NGAL, and CHI3L1 was 2.8 +/- 2.3 ng/mL, 349.2 +/- 111.4 ng/mL, and 185.5 +/- 66.8 ng/mL, respectively. During a 3-year follow-up period, the plasma level of PTX3 was an independent predictor for AVF functional patency loss (per 1 ng/mL increase, HR 1.112 [95% CI: 1.001-1.235], p = 0.048). Besides, patients with higher plasma levels of PTX3 were more likely to suffer from cardiovascular mortality (per 1 ng/mL increase, HR 1.320 [95% CI: 1.023-1.703], p = 0.033), infectious mortality (per 1 ng/mL increase, HR 1.394 [95% CI: 1.099-1.769], p = 0.006), and all-cause mortality (per 1 ng/mL increase, HR 1.233 [95% CI: 1.031-1.476], p = 0.022). Conclusions: The plasma level of PTX3, not NGAL or CHI3L1, was associated with higher risks of AVF functional patency loss in chronic hemodialysis patients, showing its value in reflecting AVF endothelial dysfunction. Furthermore, PTX3 also predicts mortality in chronic hemodialysis patients.
引用
收藏
页码:148 / 156
页数:9
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