Johann Lambeck , Axel Schläger , Nils Venhoff , Cornelius Weiller , Christoph Strecker , Matthias Reinhard
{"title":"Vertebral artery involvement in giant cell arteritis: Symptoms, treatment and outcome","authors":"Johann Lambeck , Axel Schläger , Nils Venhoff , Cornelius Weiller , Christoph Strecker , Matthias Reinhard","doi":"10.1016/j.jstrokecerebrovasdis.2025.108260","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><div>Giant cell arteritis (GCA) of the vertebral artery (VA) is a rare but serious cause of ischemic stroke, however, the long-term clinical and sonographic course of GCA patients with VA involvement (VA+) is poorly understood.</div></div><div><h3>Methods</h3><div>All patients with suspected GCA who were consecutively referred to our ultrasound (US) lab over a 12-year-period were analyzed. US examination (GCA-specific) of the cranial and cervical arteries was performed. Patients with a positive US diagnosis of GCA were identified, and further analysis was restricted to VA+ patients. Follow-up data were extracted from our hospital database.</div></div><div><h3>Results</h3><div>Among the 785 patients screened for GCA, 220 showed typical US-based findings for GCA, 74 (34 %) of whom were VA+. Fourteen VA+ patients (19 %) had vertebrobasilar ischemia at presentation (11 stroke, 3 TIA). Cerebral ischemia was more frequent in patients with severe compared to moderate VA occlusive disease (35 % vs 9 %; <em>p</em> = 0.0099, OR = 5.39, 95 % CI 1.50–9.42). Two patients died from severe initial stroke. Follow-up data were available for 34 VA+ patients (46 % of all VA+ patients; median period, 740 days), where 13 (38 %) displayed stable US alterations to the VA, 14 (41 %) a regression and 7 (21 %) a progression of stenosis. Four patients (12 %) had vertebrobasilar re-stroke, 3 of them within 30days of treatment initiation.</div></div><div><h3>Conclusion</h3><div>One-third-of patients with cranial GCA were VA+, 19 % of whom had vertebrobasilar stroke, of which most had severe VA occlusive disease. Significant rates of stenosis progression and recurrent stroke therefore call for early intensive immunosuppressive treatment.</div></div>","PeriodicalId":54368,"journal":{"name":"Journal of Stroke & Cerebrovascular Diseases","volume":"34 4","pages":"Article 108260"},"PeriodicalIF":1.8000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Stroke & Cerebrovascular Diseases","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1052305725000394","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/12 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Background
Giant cell arteritis (GCA) of the vertebral artery (VA) is a rare but serious cause of ischemic stroke, however, the long-term clinical and sonographic course of GCA patients with VA involvement (VA+) is poorly understood.
Methods
All patients with suspected GCA who were consecutively referred to our ultrasound (US) lab over a 12-year-period were analyzed. US examination (GCA-specific) of the cranial and cervical arteries was performed. Patients with a positive US diagnosis of GCA were identified, and further analysis was restricted to VA+ patients. Follow-up data were extracted from our hospital database.
Results
Among the 785 patients screened for GCA, 220 showed typical US-based findings for GCA, 74 (34 %) of whom were VA+. Fourteen VA+ patients (19 %) had vertebrobasilar ischemia at presentation (11 stroke, 3 TIA). Cerebral ischemia was more frequent in patients with severe compared to moderate VA occlusive disease (35 % vs 9 %; p = 0.0099, OR = 5.39, 95 % CI 1.50–9.42). Two patients died from severe initial stroke. Follow-up data were available for 34 VA+ patients (46 % of all VA+ patients; median period, 740 days), where 13 (38 %) displayed stable US alterations to the VA, 14 (41 %) a regression and 7 (21 %) a progression of stenosis. Four patients (12 %) had vertebrobasilar re-stroke, 3 of them within 30days of treatment initiation.
Conclusion
One-third-of patients with cranial GCA were VA+, 19 % of whom had vertebrobasilar stroke, of which most had severe VA occlusive disease. Significant rates of stenosis progression and recurrent stroke therefore call for early intensive immunosuppressive treatment.
椎动脉巨细胞动脉炎(GCA)是一种罕见但严重的缺血性脑卒中病因,然而,GCA合并椎动脉累及(VA+)患者的长期临床和超声病程尚不清楚。方法对12年来我院超声实验室收治的疑似GCA患者进行分析。行颅颈动脉超声检查(gca特异性)。鉴别出美国诊断为GCA阳性的患者,进一步分析仅限于VA+患者。随访数据从我院数据库中提取。结果在筛查的785例GCA患者中,220例显示典型的基于美国的GCA表现,其中74例(34%)为VA+。14例VA+患者(19%)出现椎基底动脉缺血(11例卒中,3例TIA)。脑缺血在严重VA闭塞性疾病患者中比在中度VA闭塞性疾病患者中更常见(35% vs 9%;p = 0.0099, OR = 5.39, 95% CI 1.50-9.42)。两名患者死于严重的初期中风。34例VA+患者可获得随访数据(占所有VA+患者的46%;中位时间为740天),其中13例(38%)表现为VA的稳定US改变,14例(41%)表现为退化,7例(21%)表现为狭窄进展。4例患者(12%)发生椎基底动脉再卒中,其中3例在治疗开始后30天内发生。结论颅脑GCA患者中有1 / 3为VA+,其中19%合并椎基底动脉卒中,其中大部分合并严重的VA闭塞性疾病。因此,明显的狭窄进展率和卒中复发率要求早期强化免疫抑制治疗。
期刊介绍:
The Journal of Stroke & Cerebrovascular Diseases publishes original papers on basic and clinical science related to the fields of stroke and cerebrovascular diseases. The Journal also features review articles, controversies, methods and technical notes, selected case reports and other original articles of special nature. Its editorial mission is to focus on prevention and repair of cerebrovascular disease. Clinical papers emphasize medical and surgical aspects of stroke, clinical trials and design, epidemiology, stroke care delivery systems and outcomes, imaging sciences and rehabilitation of stroke. The Journal will be of special interest to specialists involved in caring for patients with cerebrovascular disease, including neurologists, neurosurgeons and cardiologists.