Philippe L L'Allier, Jean-Claude Tardif, Jean Grégoire, Michel Joyal, Jacques Lespérance, Annik Fortier, Marie-Claude Guertin
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Six-month clinical and angiographic follow-up was conducted in all patients, and quantitative coronary analysis was systematically performed.</p><p><strong>Results: </strong>Levels of soluble CD40 ligand (sCD40L) and matrix metalloproteinase-2 showed a rise and fall pattern over six months, with peak levels measured at one month (P < 0.0001), while levels of soluble vascular cell adhesion molecule-1 increased after angioplasty and remained elevated at six months (P = 0.07). Plasma levels of sCD40L at one month correlated with angiographic late loss (r = 0.48, P = 0.001) and were predictive of six-month restenosis (area under receiver operating characteristic curve 0.75 [95% CI 0.61 to 0.88]).</p><p><strong>Conclusions: </strong>The results imply that inflammation persists for at least one month following angioplasty and that future therapeutic interventions targeting inflammation to prevent restenosis should be active during this period. Furthermore, the ability of sCD40L levels to predict restenosis at six months may indicate the relevance of this pathway as a therapeutic target for restenosis prevention.</p>","PeriodicalId":505916,"journal":{"name":"The Canadian journal of cardiology","volume":" ","pages":"495-500"},"PeriodicalIF":0.0000,"publicationDate":"2005-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sustained elevation of serum CD40 ligand levels one month after coronary angioplasty predicts angiographic restenosis.\",\"authors\":\"Philippe L L'Allier, Jean-Claude Tardif, Jean Grégoire, Michel Joyal, Jacques Lespérance, Annik Fortier, Marie-Claude Guertin\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Percutaneous coronary intervention induces an early inflammatory reaction. The intensity of such a reaction as measured by high-sensitivity C-reactive protein has been correlated with recurrent ischemic events, but its association with restenosis remains uncertain.</p><p><strong>Objectives: </strong>To characterize the type and duration of the postangioplasty inflammatory reaction and to identify new inflammatory markers correlating with restenosis.</p><p><strong>Methods: </strong>Fifty-three consecutive patients who underwent successful balloon angioplasty were studied. Levels of specific inflammatory markers were measured before intervention, and at one-month and six-month follow-up. Six-month clinical and angiographic follow-up was conducted in all patients, and quantitative coronary analysis was systematically performed.</p><p><strong>Results: </strong>Levels of soluble CD40 ligand (sCD40L) and matrix metalloproteinase-2 showed a rise and fall pattern over six months, with peak levels measured at one month (P < 0.0001), while levels of soluble vascular cell adhesion molecule-1 increased after angioplasty and remained elevated at six months (P = 0.07). Plasma levels of sCD40L at one month correlated with angiographic late loss (r = 0.48, P = 0.001) and were predictive of six-month restenosis (area under receiver operating characteristic curve 0.75 [95% CI 0.61 to 0.88]).</p><p><strong>Conclusions: </strong>The results imply that inflammation persists for at least one month following angioplasty and that future therapeutic interventions targeting inflammation to prevent restenosis should be active during this period. 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引用次数: 0
摘要
背景:经皮冠状动脉介入治疗可诱发早期炎症反应。高灵敏度c反应蛋白测量的这种反应强度与复发性缺血事件相关,但其与再狭窄的关系仍不确定。目的:探讨血管成形术后炎症反应的类型和持续时间,并发现与再狭窄相关的新的炎症标志物。方法:对连续53例成功行球囊血管成形术的患者进行分析。在干预前以及随访1个月和6个月时测量特定炎症标志物的水平。所有患者均进行了为期6个月的临床和血管造影随访,并系统地进行了定量的冠状动脉分析。结果:可溶性CD40配体(sCD40L)和基质金属蛋白酶-2水平在6个月内呈上升和下降趋势,在1个月内达到峰值(P < 0.0001),而血管成形术后可溶性血管细胞粘附分子-1水平升高,并在6个月内保持升高(P = 0.07)。1个月时血浆sCD40L水平与血管造影晚期损失相关(r = 0.48, P = 0.001),并可预测6个月再狭窄(受试者工作特征曲线下面积0.75 [95% CI 0.61至0.88])。结论:结果表明血管成形术后炎症至少持续一个月,未来针对炎症预防再狭窄的治疗干预应在此期间积极进行。此外,sCD40L水平在6个月时预测再狭窄的能力可能表明该途径作为预防再狭窄的治疗靶点的相关性。
Sustained elevation of serum CD40 ligand levels one month after coronary angioplasty predicts angiographic restenosis.
Background: Percutaneous coronary intervention induces an early inflammatory reaction. The intensity of such a reaction as measured by high-sensitivity C-reactive protein has been correlated with recurrent ischemic events, but its association with restenosis remains uncertain.
Objectives: To characterize the type and duration of the postangioplasty inflammatory reaction and to identify new inflammatory markers correlating with restenosis.
Methods: Fifty-three consecutive patients who underwent successful balloon angioplasty were studied. Levels of specific inflammatory markers were measured before intervention, and at one-month and six-month follow-up. Six-month clinical and angiographic follow-up was conducted in all patients, and quantitative coronary analysis was systematically performed.
Results: Levels of soluble CD40 ligand (sCD40L) and matrix metalloproteinase-2 showed a rise and fall pattern over six months, with peak levels measured at one month (P < 0.0001), while levels of soluble vascular cell adhesion molecule-1 increased after angioplasty and remained elevated at six months (P = 0.07). Plasma levels of sCD40L at one month correlated with angiographic late loss (r = 0.48, P = 0.001) and were predictive of six-month restenosis (area under receiver operating characteristic curve 0.75 [95% CI 0.61 to 0.88]).
Conclusions: The results imply that inflammation persists for at least one month following angioplasty and that future therapeutic interventions targeting inflammation to prevent restenosis should be active during this period. Furthermore, the ability of sCD40L levels to predict restenosis at six months may indicate the relevance of this pathway as a therapeutic target for restenosis prevention.