{"title":"他汀类药物治疗后动脉粥样硬化分支斑块的时间演变和临床意义的初步结果。","authors":"Yen-Chu Huang, Yuan-Hsiung Tsai, Leng-Chieh Lin, Hsu-Huei Weng, Jiann-Der Lee, Jen-Tsung Yang","doi":"10.1177/17562864241273902","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Branch atheromatous disease (BAD) is a primary cause of early neurological deterioration (END) in penetrating artery occlusion, leading to poor functional outcomes. While it has been proposed to classify BAD under large artery atherosclerosis, uncertainty exists regarding the optimal treatment strategy, including cholesterol-lowering targets.</p><p><strong>Objectives: </strong>We aimed to assess the clinical implications and temporal changes of atherosclerotic plaques before and after high-intensity statin treatment.</p><p><strong>Design: </strong>This is a high-resolution vessel-wall imaging sub-analysis of the trial of Statin and Dual Antiplatelet Therapy in Preventing Early Neurological Deterioration in Branch Atheromatous Disease (SATBRAD).</p><p><strong>Methods: </strong>In this prospective, single-group cohort study, participants in the treatment arm of the SATBRAD trial received early dual antiplatelet therapy and high-intensity statin treatment. The majority of these participants subsequently underwent high-resolution vessel-wall magnetic resonance imaging (MRI). Those with atheromatous plaques in the parent artery continued high-intensity statin treatment for 6 months, followed by a repeat MRI to monitor plaque changes.</p><p><strong>Results: </strong>There were 57 patients who underwent vessel-wall imaging and 24 exhibited contrast-enhanced plaques. Patients with contrast-enhanced plaques showed higher rates of END (29.2% vs 6.1%, <i>p</i> = 0.027), perfusion defects (62.5% vs 24.2%, <i>p</i> = 0.004), and lower rates of good outcomes at 3 months (50.0% vs 81.8%, <i>p</i> = 0.011). After adjusting for confounding factors, contrast-enhanced plaque had a negative impact on achieving a good outcome at 3 months (adjusted odds ratio = 0.04; 95% confidence interval = <0.01-0.60). Following high-intensity statin treatment in 36 patients, there was a notable reduction in stenosis (33.7% vs 29.3%, <i>p</i> = 0.005) and contrast-enhanced plaque volume (16.3 vs 11.6 mm<sup>3</sup>, <i>p</i> = 0.015).</p><p><strong>Conclusion: </strong>The study highlighted the association between contrast-enhanced atherosclerotic plaques, END, and poor functional outcomes, with high-intensity treatment leading to plaque volume reduction. These results underscore the shared pathology between BAD and intracranial atherosclerosis, emphasizing the necessity for further research and tailored treatment strategies for BAD.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov; Identifier: NCT04824911 (https://clinicaltrials.gov/study/NCT04824911).</p>","PeriodicalId":22980,"journal":{"name":"Therapeutic Advances in Neurological Disorders","volume":"17 ","pages":"17562864241273902"},"PeriodicalIF":4.7000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11418250/pdf/","citationCount":"0","resultStr":"{\"title\":\"Preliminary results on temporal evolution and clinical implications of atherosclerotic plaque in branch atheromatous disease after statin treatment.\",\"authors\":\"Yen-Chu Huang, Yuan-Hsiung Tsai, Leng-Chieh Lin, Hsu-Huei Weng, Jiann-Der Lee, Jen-Tsung Yang\",\"doi\":\"10.1177/17562864241273902\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Branch atheromatous disease (BAD) is a primary cause of early neurological deterioration (END) in penetrating artery occlusion, leading to poor functional outcomes. While it has been proposed to classify BAD under large artery atherosclerosis, uncertainty exists regarding the optimal treatment strategy, including cholesterol-lowering targets.</p><p><strong>Objectives: </strong>We aimed to assess the clinical implications and temporal changes of atherosclerotic plaques before and after high-intensity statin treatment.</p><p><strong>Design: </strong>This is a high-resolution vessel-wall imaging sub-analysis of the trial of Statin and Dual Antiplatelet Therapy in Preventing Early Neurological Deterioration in Branch Atheromatous Disease (SATBRAD).</p><p><strong>Methods: </strong>In this prospective, single-group cohort study, participants in the treatment arm of the SATBRAD trial received early dual antiplatelet therapy and high-intensity statin treatment. The majority of these participants subsequently underwent high-resolution vessel-wall magnetic resonance imaging (MRI). Those with atheromatous plaques in the parent artery continued high-intensity statin treatment for 6 months, followed by a repeat MRI to monitor plaque changes.</p><p><strong>Results: </strong>There were 57 patients who underwent vessel-wall imaging and 24 exhibited contrast-enhanced plaques. Patients with contrast-enhanced plaques showed higher rates of END (29.2% vs 6.1%, <i>p</i> = 0.027), perfusion defects (62.5% vs 24.2%, <i>p</i> = 0.004), and lower rates of good outcomes at 3 months (50.0% vs 81.8%, <i>p</i> = 0.011). After adjusting for confounding factors, contrast-enhanced plaque had a negative impact on achieving a good outcome at 3 months (adjusted odds ratio = 0.04; 95% confidence interval = <0.01-0.60). Following high-intensity statin treatment in 36 patients, there was a notable reduction in stenosis (33.7% vs 29.3%, <i>p</i> = 0.005) and contrast-enhanced plaque volume (16.3 vs 11.6 mm<sup>3</sup>, <i>p</i> = 0.015).</p><p><strong>Conclusion: </strong>The study highlighted the association between contrast-enhanced atherosclerotic plaques, END, and poor functional outcomes, with high-intensity treatment leading to plaque volume reduction. These results underscore the shared pathology between BAD and intracranial atherosclerosis, emphasizing the necessity for further research and tailored treatment strategies for BAD.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov; Identifier: NCT04824911 (https://clinicaltrials.gov/study/NCT04824911).</p>\",\"PeriodicalId\":22980,\"journal\":{\"name\":\"Therapeutic Advances in Neurological Disorders\",\"volume\":\"17 \",\"pages\":\"17562864241273902\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11418250/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Therapeutic Advances in Neurological Disorders\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1177/17562864241273902\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Therapeutic Advances in Neurological Disorders","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/17562864241273902","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景:分支动脉粥样硬化症(BAD)是穿透性动脉闭塞早期神经功能恶化(END)的主要原因,会导致不良的功能预后。虽然有人建议将 BAD 归为大动脉粥样硬化,但最佳治疗策略(包括降低胆固醇目标)仍存在不确定性:我们旨在评估高强度他汀治疗前后动脉粥样硬化斑块的临床意义和时间变化:设计:这是他汀类药物和双联抗血小板疗法预防动脉粥样硬化性疾病早期神经功能恶化试验(SATBRAD)的一项高分辨率血管壁成像子分析:在这项前瞻性单组队列研究中,SATBRAD 试验治疗组的参与者接受了早期双联抗血小板疗法和高强度他汀类药物治疗。大多数参与者随后接受了高分辨率血管壁磁共振成像(MRI)检查。母动脉中有粥样斑块的患者继续接受高强度他汀类药物治疗6个月,然后再次接受磁共振成像检查以监测斑块的变化:共有 57 名患者接受了血管壁成像检查,其中 24 名患者的斑块呈对比增强。对比增强斑块患者的END(29.2% vs 6.1%,p = 0.027)和灌注缺损(62.5% vs 24.2%,p = 0.004)发生率较高,3个月后的良好预后发生率较低(50.0% vs 81.8%,p = 0.011)。调整混杂因素后,对比度增强斑块对3个月后的良好预后有负面影响(调整赔率=0.04;95%置信区间=p=0.005),对比度增强斑块体积(16.3 vs 11.6 mm3,p=0.015)也有负面影响:该研究强调了造影剂增强型动脉粥样硬化斑块、END和不良功能预后之间的关联,高强度治疗可减少斑块体积。这些结果突出了BAD与颅内动脉粥样硬化之间的共同病理,强调了进一步研究和针对BAD的治疗策略的必要性:试验注册:ClinicalTrials.gov;Identifier:NCT04824911 (https://clinicaltrials.gov/study/NCT04824911)。
Preliminary results on temporal evolution and clinical implications of atherosclerotic plaque in branch atheromatous disease after statin treatment.
Background: Branch atheromatous disease (BAD) is a primary cause of early neurological deterioration (END) in penetrating artery occlusion, leading to poor functional outcomes. While it has been proposed to classify BAD under large artery atherosclerosis, uncertainty exists regarding the optimal treatment strategy, including cholesterol-lowering targets.
Objectives: We aimed to assess the clinical implications and temporal changes of atherosclerotic plaques before and after high-intensity statin treatment.
Design: This is a high-resolution vessel-wall imaging sub-analysis of the trial of Statin and Dual Antiplatelet Therapy in Preventing Early Neurological Deterioration in Branch Atheromatous Disease (SATBRAD).
Methods: In this prospective, single-group cohort study, participants in the treatment arm of the SATBRAD trial received early dual antiplatelet therapy and high-intensity statin treatment. The majority of these participants subsequently underwent high-resolution vessel-wall magnetic resonance imaging (MRI). Those with atheromatous plaques in the parent artery continued high-intensity statin treatment for 6 months, followed by a repeat MRI to monitor plaque changes.
Results: There were 57 patients who underwent vessel-wall imaging and 24 exhibited contrast-enhanced plaques. Patients with contrast-enhanced plaques showed higher rates of END (29.2% vs 6.1%, p = 0.027), perfusion defects (62.5% vs 24.2%, p = 0.004), and lower rates of good outcomes at 3 months (50.0% vs 81.8%, p = 0.011). After adjusting for confounding factors, contrast-enhanced plaque had a negative impact on achieving a good outcome at 3 months (adjusted odds ratio = 0.04; 95% confidence interval = <0.01-0.60). Following high-intensity statin treatment in 36 patients, there was a notable reduction in stenosis (33.7% vs 29.3%, p = 0.005) and contrast-enhanced plaque volume (16.3 vs 11.6 mm3, p = 0.015).
Conclusion: The study highlighted the association between contrast-enhanced atherosclerotic plaques, END, and poor functional outcomes, with high-intensity treatment leading to plaque volume reduction. These results underscore the shared pathology between BAD and intracranial atherosclerosis, emphasizing the necessity for further research and tailored treatment strategies for BAD.
期刊介绍:
Therapeutic Advances in Neurological Disorders is a peer-reviewed, open access journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of neurology. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in neurology, providing a forum in print and online for publishing the highest quality articles in this area.