One-Year Radiologic Progression in Sporadic and Hereditary Cerebral Amyloid Angiopathy.

IF 7.7 1区 医学 Q1 CLINICAL NEUROLOGY
Neurology Pub Date : 2025-05-13 Epub Date: 2025-04-08 DOI:10.1212/WNL.0000000000213546
Maaike C van der Plas, Emma A Koemans, Manon R Schipper, Sabine Voigt, Ingeborg Rasing, Reinier G J van der Zwet, Kanishk Kaushik, Rosemarie van Dort, Sanne Schriemer, Thijs W van Harten, Erik van Zwet, Ellis S van Etten, Matthias J P van Osch, Gisela M Terwindt, Marianne van Walderveen, Marieke J H Wermer
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引用次数: 0

Abstract

Background and objectives: Knowledge on the short-term progression of cerebral amyloid angiopathy (CAA) is important for clinical practice and the design of clinical treatment trials. We investigated the 1-year progression of CAA-related MRI markers in sporadic (sCAA) and Dutch-type hereditary (D-CAA).

Methods: Participants were included from 2 prospective cohort studies. 3T-MRI was performed at baseline and after 1 year. We assessed macrobleeds, cerebral microbleeds (CMBs), cortical superficial siderosis (cSS), convexity subarachnoid hemorrhages (cSAHs), white matter hyperintensities (WMH), enlarged centrum semiovale perivascular spaces (CSO-EPVS), and visually stimulated blood oxygenation level-dependent (BOLD) fMRI parameters. Progression was defined as increase in number of macrobleeds or CMBs, new focus or extension of cSS, increase in CSO-EPVS category, or volume increase of >10% of WMH. Multivariable regression analyses were performed to determine factors associated with progression and the association between events related to parenchymal injury (cSAH, macrobleeds) and radiologic progression.

Results: We included 98 participants (47% women): 55 with sCAA (mean age 70 years), 28 with symptomatic D-CAA (mean age 59 years), and 15 with presymptomatic D-CAA (mean age 45 years). Progression of >1 MRI markers was seen in all 83 (100%) participants with sCAA and symptomatic D-CAA and in 9 (60%) with presymptomatic D-CAA. The number of CMBs showed the largest progression in sCAA (98%; median increase 24) and symptomatic D-CAA (100%; median increase 58). WMH volume (>10% increase in 70%; mean increase 1.2 mL) was most progressive in presymptomatic D-CAA. A decrease in the upslope of the visually evoked BOLD response was observed for most patients. Symptomatic D-CAA status was associated with more overall progression (adjusted odds ratio [aOR] 9.7; 95% CI 1.7-54.2), CMB (adjusted relative risk [aRR] 2.47; 95% CI 1.5-4.1), and WMH volume progression (β 2.52; 95% CI 0.3-4.8). Baseline CMB count (aRR 1.002; 95% CI 1.001-1.002) was associated with CMB progression and cSS presence at baseline (aOR 8.16; 95% CI 2.6-25.4) with cSS progression. cSS progression was also associated with cSAH and macrobleeds (aOR 21,029; 95% CI 2.042-216.537).

Discussion: CAA is a radiologically progressive disease even in the short-term. After 1 year, all symptomatic and most of the presymptomatic participants showed progression of at least 1 MRI-marker. CMBs and WMH volume (in symptomatic CAA) and WMH volume (in presymptomatic CAA) are the most promising markers to track short-term progression in future trials.

散发性和遗传性脑淀粉样血管病的一年影像学进展。
背景与目的:了解脑淀粉样血管病(CAA)的短期进展对临床实践和临床治疗试验的设计具有重要意义。我们研究了散发性(sCAA)和荷兰型遗传性(D-CAA)中caa相关MRI标志物的1年进展情况。方法:参与者来自2项前瞻性队列研究。在基线和1年后分别进行3T-MRI检查。我们评估了大出血、脑微出血(CMBs)、皮质浅表性铁质沉积(cSS)、凸出性蛛网膜下腔出血(cSAHs)、白质高信号(WMH)、半瓣膜中心周围血管间隙增大(CSO-EPVS)和视觉刺激血氧水平依赖(BOLD)功能磁共振成像参数。进展被定义为大出血或CMBs数量的增加,cSS的新焦点或扩展,CSO-EPVS类别的增加,或WMH体积增加10 ~ 10%。进行多变量回归分析以确定与进展相关的因素以及与实质损伤(cSAH、大出血)相关的事件与放射学进展之间的关联。结果:我们纳入了98名参与者(47%为女性):55名sCAA患者(平均年龄70岁),28名症状性D-CAA患者(平均年龄59岁),15名症状前D-CAA患者(平均年龄45岁)。83名sCAA和症状性D-CAA患者(100%)和9名症状前D-CAA患者(60%)的bbb1 MRI标志物进展。CMBs的数量在sCAA中表现出最大的进展(98%;中位数增加24)和症状性D-CAA (100%;中位数增加58)。WMH体积(bbb10 %)增加70%;平均升高1.2 mL)在症状前D-CAA中最具进展性。在大多数患者中观察到视觉诱发的BOLD反应的上坡下降。症状性D-CAA状态与更大的总体进展相关(调整优势比[aOR] 9.7;95% CI 1.7-54.2), CMB(调整相对危险度[aRR] 2.47;95% CI 1.5-4.1), WMH体积进展(β 2.52;95% ci 0.3-4.8)。基线CMB计数(aRR 1.002;95% CI 1.001-1.002)与基线时CMB进展和cSS存在相关(aOR 8.16;95% CI为2.6-25.4)。cSS进展也与cah和大出血相关(aOR 21,029;95% ci 2.042-216.537)。讨论:即使在短期内,CAA也是一种放射学进展性疾病。1年后,所有有症状的和大多数有症状前的参与者显示出至少1个mri标记物的进展。CMBs和WMH体积(症状性CAA)和WMH体积(症状前CAA)是未来试验中最有希望追踪短期进展的标志物。
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来源期刊
Neurology
Neurology 医学-临床神经学
CiteScore
12.20
自引率
4.00%
发文量
1973
审稿时长
2-3 weeks
期刊介绍: Neurology, the official journal of the American Academy of Neurology, aspires to be the premier peer-reviewed journal for clinical neurology research. Its mission is to publish exceptional peer-reviewed original research articles, editorials, and reviews to improve patient care, education, clinical research, and professionalism in neurology. As the leading clinical neurology journal worldwide, Neurology targets physicians specializing in nervous system diseases and conditions. It aims to advance the field by presenting new basic and clinical research that influences neurological practice. The journal is a leading source of cutting-edge, peer-reviewed information for the neurology community worldwide. Editorial content includes Research, Clinical/Scientific Notes, Views, Historical Neurology, NeuroImages, Humanities, Letters, and position papers from the American Academy of Neurology. The online version is considered the definitive version, encompassing all available content. Neurology is indexed in prestigious databases such as MEDLINE/PubMed, Embase, Scopus, Biological Abstracts®, PsycINFO®, Current Contents®, Web of Science®, CrossRef, and Google Scholar.
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