{"title":"缺血性中风或 TIA 患者氯吡格雷耐受性和 ABCD-GENE 评分与长期临床预后的关系。","authors":"","doi":"10.1016/j.neurol.2024.03.011","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p><span>Clopidogrel resistance (CR) is associated with adverse clinical outcomes in </span>acute ischemic stroke<span> or transient ischemic attack (TIA) patients. However, whether CR affects the long-term clinical prognosis remains to be clarified. The ABCD-GENE score is a novel risk model that identifies CR in cardiovascular disease patients; its diagnostic ability and application in ischemic stroke or TIA remain to be studied. This study aimed to investigate the diagnostic ability of the ABCD-GENE score for CR and analyze the relationship between CR and long-term clinical prognosis in patients with ischemic stroke or TIA.</span></p></div><div><h3>Methods</h3><p><span><span>From January 2018 to January 2021, 251 ischemic stroke or TIA patients who were treated with clopidogrel for more than three months after onset and maintained the medication until the follow-up time were enrolled, and platelet reactivity was detected by </span>thromboelastography. </span><span><span>CYP2C19</span></span> gene analysis was performed. Adverse clinical outcomes were recorded from 3<!--> <!-->months after onset. The median follow-up time was 878<!--> <!-->days.</p></div><div><h3>Results</h3><p><span>The prevalence of CR was 33.9%. The proportion of CYP2C19 loss-of-function carriers was 62.2%. The ABCD-GENE score</span> <!-->≥<!--> <!-->10 was independently associated with CR (OR<!--> <!-->=<!--> <!-->1.82, 95% CI: 1.02–3.24, <em>P</em> <!-->=<!--> <!-->0.041), and the C-statistic value of the score (as a binary and integer variable) on CR was 0.58 and 0.63, respectively. The risk of long-term adverse clinical outcomes was not significantly different between CR and clopidogrel sensitive groups (12.94% vs. 11.44%, HR<!--> <!-->=<!--> <!-->1.22, 95% CI: 0.57–2.62, <em>P</em> <!-->=<!--> <!-->0.603). A similar result was observed between ABCD-GENE score<!--> <!-->≥<!--> <!-->10 and ABCD-GENE score<!--> <!--><<!--> <!-->10 groups (10.38% vs. 12.64%, HR<!--> <!-->=<!--> <!-->1.19, 95% CI: 0.55–2.60, <em>P</em> <!-->=<!--> <!-->0.666).</p></div><div><h3>Conclusions</h3><p>In ischemic stroke or TIA patients, the ABCD-GENE score could identify the risk of CR. CR was not associated with long-term adverse clinical outcomes.</p></div>","PeriodicalId":21321,"journal":{"name":"Revue neurologique","volume":"180 7","pages":"Pages 682-688"},"PeriodicalIF":2.8000,"publicationDate":"2024-05-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association of clopidogrel resistance and ABCD-GENE score with long-term clinical prognosis in patients with ischemic stroke or TIA\",\"authors\":\"\",\"doi\":\"10.1016/j.neurol.2024.03.011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p><span>Clopidogrel resistance (CR) is associated with adverse clinical outcomes in </span>acute ischemic stroke<span> or transient ischemic attack (TIA) patients. However, whether CR affects the long-term clinical prognosis remains to be clarified. The ABCD-GENE score is a novel risk model that identifies CR in cardiovascular disease patients; its diagnostic ability and application in ischemic stroke or TIA remain to be studied. This study aimed to investigate the diagnostic ability of the ABCD-GENE score for CR and analyze the relationship between CR and long-term clinical prognosis in patients with ischemic stroke or TIA.</span></p></div><div><h3>Methods</h3><p><span><span>From January 2018 to January 2021, 251 ischemic stroke or TIA patients who were treated with clopidogrel for more than three months after onset and maintained the medication until the follow-up time were enrolled, and platelet reactivity was detected by </span>thromboelastography. </span><span><span>CYP2C19</span></span> gene analysis was performed. Adverse clinical outcomes were recorded from 3<!--> <!-->months after onset. The median follow-up time was 878<!--> <!-->days.</p></div><div><h3>Results</h3><p><span>The prevalence of CR was 33.9%. The proportion of CYP2C19 loss-of-function carriers was 62.2%. The ABCD-GENE score</span> <!-->≥<!--> <!-->10 was independently associated with CR (OR<!--> <!-->=<!--> <!-->1.82, 95% CI: 1.02–3.24, <em>P</em> <!-->=<!--> <!-->0.041), and the C-statistic value of the score (as a binary and integer variable) on CR was 0.58 and 0.63, respectively. The risk of long-term adverse clinical outcomes was not significantly different between CR and clopidogrel sensitive groups (12.94% vs. 11.44%, HR<!--> <!-->=<!--> <!-->1.22, 95% CI: 0.57–2.62, <em>P</em> <!-->=<!--> <!-->0.603). A similar result was observed between ABCD-GENE score<!--> <!-->≥<!--> <!-->10 and ABCD-GENE score<!--> <!--><<!--> <!-->10 groups (10.38% vs. 12.64%, HR<!--> <!-->=<!--> <!-->1.19, 95% CI: 0.55–2.60, <em>P</em> <!-->=<!--> <!-->0.666).</p></div><div><h3>Conclusions</h3><p>In ischemic stroke or TIA patients, the ABCD-GENE score could identify the risk of CR. CR was not associated with long-term adverse clinical outcomes.</p></div>\",\"PeriodicalId\":21321,\"journal\":{\"name\":\"Revue neurologique\",\"volume\":\"180 7\",\"pages\":\"Pages 682-688\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-05-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Revue neurologique\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0035378724005162\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revue neurologique","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0035378724005162","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:氯吡格雷耐药(CR)与急性缺血性卒中或短暂性脑缺血发作(TIA)患者的不良临床结局有关。然而,CR 是否会影响长期临床预后仍有待明确。ABCD-GENE 评分是一种新型风险模型,可识别心血管疾病患者的 CR,但其在缺血性卒中或 TIA 中的诊断能力和应用仍有待研究。本研究旨在探讨ABCD-GENE评分对CR的诊断能力,并分析缺血性卒中或TIA患者CR与长期临床预后的关系:从2018年1月至2021年1月,入选251例缺血性卒中或TIA患者,这些患者在发病后接受氯吡格雷治疗3个月以上,并坚持服药至随访时间,通过血栓弹力图检测血小板反应性。进行了 CYP2C19 基因分析。从发病后 3 个月开始记录不良临床结果。中位随访时间为 878 天:结果:CR的发病率为33.9%。结果:CR的发病率为33.9%,CYP2C19功能缺失携带者的比例为62.2%。ABCD-GENE评分≥10与CR独立相关(OR=1.82,95% CI:1.02-3.24,P=0.041),评分(二元变量和整数变量)对CR的C统计值分别为0.58和0.63。CR组和氯吡格雷敏感组的长期不良临床结局风险无明显差异(12.94% vs. 11.44%,HR=1.22,95% CI:0.57-2.62,P=0.603)。在 ABCD-GENE 评分≥10 和 ABCD-GENE 评分之间也观察到类似的结果:在缺血性卒中或 TIA 患者中,ABCD-GENE 评分可识别 CR 风险。CR 与长期不良临床结局无关。
Association of clopidogrel resistance and ABCD-GENE score with long-term clinical prognosis in patients with ischemic stroke or TIA
Background
Clopidogrel resistance (CR) is associated with adverse clinical outcomes in acute ischemic stroke or transient ischemic attack (TIA) patients. However, whether CR affects the long-term clinical prognosis remains to be clarified. The ABCD-GENE score is a novel risk model that identifies CR in cardiovascular disease patients; its diagnostic ability and application in ischemic stroke or TIA remain to be studied. This study aimed to investigate the diagnostic ability of the ABCD-GENE score for CR and analyze the relationship between CR and long-term clinical prognosis in patients with ischemic stroke or TIA.
Methods
From January 2018 to January 2021, 251 ischemic stroke or TIA patients who were treated with clopidogrel for more than three months after onset and maintained the medication until the follow-up time were enrolled, and platelet reactivity was detected by thromboelastography. CYP2C19 gene analysis was performed. Adverse clinical outcomes were recorded from 3 months after onset. The median follow-up time was 878 days.
Results
The prevalence of CR was 33.9%. The proportion of CYP2C19 loss-of-function carriers was 62.2%. The ABCD-GENE score ≥ 10 was independently associated with CR (OR = 1.82, 95% CI: 1.02–3.24, P = 0.041), and the C-statistic value of the score (as a binary and integer variable) on CR was 0.58 and 0.63, respectively. The risk of long-term adverse clinical outcomes was not significantly different between CR and clopidogrel sensitive groups (12.94% vs. 11.44%, HR = 1.22, 95% CI: 0.57–2.62, P = 0.603). A similar result was observed between ABCD-GENE score ≥ 10 and ABCD-GENE score < 10 groups (10.38% vs. 12.64%, HR = 1.19, 95% CI: 0.55–2.60, P = 0.666).
Conclusions
In ischemic stroke or TIA patients, the ABCD-GENE score could identify the risk of CR. CR was not associated with long-term adverse clinical outcomes.
期刊介绍:
The first issue of the Revue Neurologique, featuring an original article by Jean-Martin Charcot, was published on February 28th, 1893. Six years later, the French Society of Neurology (SFN) adopted this journal as its official publication in the year of its foundation, 1899.
The Revue Neurologique was published throughout the 20th century without interruption and is indexed in all international databases (including Current Contents, Pubmed, Scopus). Ten annual issues provide original peer-reviewed clinical and research articles, and review articles giving up-to-date insights in all areas of neurology. The Revue Neurologique also publishes guidelines and recommendations.
The Revue Neurologique publishes original articles, brief reports, general reviews, editorials, and letters to the editor as well as correspondence concerning articles previously published in the journal in the correspondence column.