Cardiovascular Center, National Taiwan University Hospital, Hsinchu Branch, Institute of Biomedical Engineering, National Tsing-Hua University, Hsinchu, Taiwan.
College of Medicine, National Taiwan University and School of Medicine and.
Clin J Am Soc Nephrol. 2017 Jan 6;12(1):113-121. doi: 10.2215/CJN.04030416. Epub 2016 Oct 26.
Inflammation is relevant in restenosis of atherosclerotic vascular diseases, but its role in dialysis arteriovenous fistula remains unknown. In animal studies, upregulation of monocyte chemoattractant protein-1 has been shown in venous segments of arteriovenous fistula. We, therefore, aimed to investigate serial changes in circulating monocyte chemoattractant protein-1 after percutaneous transluminal angioplasty of dialysis arteriovenous fistulas and its relation to restenosis.
DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Fifty-nine patients with dysfunctional arteriovenous fistulas that were referred for percutaneous transluminal angioplasty were enrolled prospectively between January of 2010 and July of 2012. Three of them were excluded due to percutaneous transluminal angioplasty failure or acute infection. Blood was sampled from arteriovenous fistulas at baseline, 2 days, 2 weeks, and 3 months after percutaneous transluminal angioplasty. Clinical follow-up was continued monthly for 3 months. Angiographic follow-up was arranged at the end of 3 months. Seventeen patients without significant stenosis were enrolled as the control group.
Fifty-six patients completed clinical follow-up. Significant increases in monocyte chemoattractant protein-1 were observed at 2 days and 2 weeks (both P<0.001) after percutaneous transluminal angioplasty. Twenty-three (41%) patients had symptomatic restenosis. The restenosis group had a higher percentage change in monocyte chemoattractant protein-1 levels at 2 days (median =47%; interquartile range, 27%-65% versus median =17%; interquartile range, 10%-25%; P<0.001) after percutaneous transluminal angioplasty compared with the patent group. Fifty-two patients completed angiographic follow-up. A positive correlation between relative luminal loss and monocyte chemoattractant protein-1 increase at 2 days after percutaneous transluminal angioplasty was found (r=0.53; P<0.001). In multivariate analysis, postangioplasty monocyte chemoattractant protein-1 increase at 2 days was an independent predictor of restenosis. Using receiver operator characteristic analysis, >25% postangioplasty increase of monocyte chemoattractant protein-1 was significantly associated with restenosis after percutaneous transluminal angioplasty (hazard ratio, 5.36; 95% confidence interval, 1.81 to 15.8).
Circulating monocyte chemoattractant protein-1 levels were elevated 2 days and 2 weeks after percutaneous transluminal angioplasty. Early postangioplasty increase of monocyte chemoattractant protein-1 level was associated with restenosis of arteriovenous fistulas.
炎症与动脉粥样硬化性血管疾病的再狭窄有关,但它在透析动静脉瘘中的作用尚不清楚。在动物研究中,已经观察到静脉段动静脉瘘中的单核细胞趋化蛋白-1上调。因此,我们旨在研究经皮腔内血管成形术后循环单核细胞趋化蛋白-1的系列变化及其与再狭窄的关系。
设计、地点、参与者和测量:2010 年 1 月至 2012 年 7 月,前瞻性纳入 59 例功能障碍性动静脉瘘患者,进行经皮腔内血管成形术。由于经皮腔内血管成形术失败或急性感染,其中 3 例被排除在外。在经皮腔内血管成形术之前、术后 2 天、2 周和 3 个月从动静脉瘘取血。临床随访持续 3 个月。在 3 个月结束时安排血管造影随访。17 例无明显狭窄的患者被纳入对照组。
56 例患者完成临床随访。经皮腔内血管成形术后 2 天和 2 周时(均 P<0.001),单核细胞趋化蛋白-1显著增加。23 例(41%)患者出现有症状的再狭窄。再狭窄组在经皮腔内血管成形术后 2 天(中位数=47%;四分位距,27%-65%比中位数=17%;四分位距,10%-25%;P<0.001)的单核细胞趋化蛋白-1水平百分比变化更大。52 例患者完成了血管造影随访。发现经皮腔内血管成形术后 2 天相对管腔丢失与单核细胞趋化蛋白-1增加呈正相关(r=0.53;P<0.001)。在多变量分析中,经皮腔内血管成形术后 2 天的单核细胞趋化蛋白-1增加是再狭窄的独立预测因子。使用受试者工作特征分析,经皮腔内血管成形术后单核细胞趋化蛋白-1增加>25%与再狭窄显著相关(危险比,5.36;95%置信区间,1.81 至 15.8)。
经皮腔内血管成形术后 2 天和 2 周时循环单核细胞趋化蛋白-1水平升高。经皮腔内血管成形术后早期单核细胞趋化蛋白-1水平升高与动静脉瘘再狭窄有关。