Departments of 1 Radiology.
Pulmonary and Critical Care Medicine, and.
J Neurosurg. 2017 Aug;127(2):302-310. doi: 10.3171/2016.7.JNS16847. Epub 2016 Oct 21.
OBJECTIVE Patients with hereditary hemorrhagic telangiectasia (HHT) are known to suffer from high rates of cerebral arteriovenous malformations (AVMs). The authors performed a systematic review and meta-analysis of the literature examining prevalence rates, characteristics, and clinical presentation of cerebral AVMs in the HHT population. METHODS To identify studies on AVM prevalence and characteristics in the HHT population, 4 databases (MEDLINE, EMBASE, Scopus and Web of Science) were searched by a reference librarian with over 30 years experience in systematic reviews and meta-analysis. The search period was January 1, 1990-March 2016. The following search terms were used: hereditary hemorrhagic telangiectasia, Osler-Weber-Rendu syndrome, AVM, brain AVM, arteriovenous malformation, arteriovenous fistula, prevalence, and epidemiology. The authors identified studies that examined the prevalence rates, characteristics, and clinical presentation of cerebral AVMs in patients with HHT. They assessed overall AVM prevalence rates as well as prevalence rates by age, sex, HHT type, and country/region. They also systematically reviewed the characteristics of AVMs, including rupture status, location, clinical presentation, angioarchitecture, and Spetzler-Martin grade. Data were analyzed using a random-effects meta-analysis model. RESULTS Thirty-nine studies were included in this meta-analysis. Thirty studies examined brain AVM prevalence rates in various HHT patient populations, and 18 studies examined AVM clinical and angiographic characteristics (9 studies examined both prevalence rates and AVM characteristics). The prevalence of brain AVMs in HHT patients was 10.4% (95% CI 7.9%-13.0%) with no significant difference between males (8.5%, 95% CI 4.9%-12.0%) and females (11.0%, 95% CI 5.9%-16.1%). Patients with HHT Type 1 (HHT1) had a significantly higher brain AVM prevalence (13.4%, 95% CI 9.5%-17.4%) compared with those with HHT Type 2 (HHT2) (2.4%, 95% CI 1.0%-3.8%) (p < 0.0001). In 55.2% (95% CI 38.3%-72.1%) of cases, the AVMs were symptomatic. Spetzler-Martin grade was 2 or less in 86.9% (95% CI 67.5%-95.2%) of patients. CONCLUSIONS The prevalence of brain AVMs in the HHT population is about 10%. HHT1 patients are significantly more likely to have brain AVMs than HHT2 patients. Most AVMs in the HHT population are symptomatic. The Spetzler-Martin grade for these lesions is 2 or less in nearly 90% of patients.
目的
遗传性出血性毛细血管扩张症(HHT)患者发生脑动静脉畸形(AVM)的比率较高。作者对评估 HHT 人群中 AVM 发生率、特征和临床表现的文献进行了系统回顾和荟萃分析。
方法
为了确定有关 HHT 人群中 AVM 发生率和特征的研究,由一位具有 30 多年系统综述和荟萃分析经验的参考馆员使用 4 个数据库(MEDLINE、EMBASE、Scopus 和 Web of Science)进行检索。检索时间为 1990 年 1 月 1 日至 2016 年 3 月。使用的检索词如下:遗传性出血性毛细血管扩张症、Osler-Weber-Rendu 综合征、AVM、脑 AVM、动静脉畸形、动静脉瘘、发生率和流行病学。作者确定了评估 HHT 患者 AVM 发生率、特征和临床表现的研究。他们评估了总体 AVM 发生率,以及按年龄、性别、HHT 类型和国家/地区划分的发生率。他们还系统地回顾了 AVM 的特征,包括破裂状态、位置、临床表现、血管构筑和 Spetzler-Martin 分级。使用随机效应荟萃分析模型进行数据分析。
结果
本荟萃分析共纳入 39 项研究。30 项研究评估了各种 HHT 患者人群中脑 AVM 的发生率,18 项研究评估了 AVM 的临床和血管造影特征(9 项研究同时评估了发生率和 AVM 特征)。HHT 患者脑 AVM 的发生率为 10.4%(95%CI 7.9%-13.0%),男性(8.5%,95%CI 4.9%-12.0%)和女性(11.0%,95%CI 5.9%-16.1%)之间无显著差异。HHT1 型(HHT1)患者脑 AVM 的发生率明显高于 HHT2 型(HHT2)患者(13.4%,95%CI 9.5%-17.4%对 2.4%,95%CI 1.0%-3.8%)(p<0.0001)。在 55.2%(95%CI 38.3%-72.1%)的病例中,AVM 有症状。86.9%(95%CI 67.5%-95.2%)的患者 Spetzler-Martin 分级为 2 级或更低。
结论
HHT 人群中脑 AVM 的发生率约为 10%。HHT1 型患者发生脑 AVM 的可能性明显高于 HHT2 型患者。HHT 人群中大多数 AVM 有症状。近 90%的患者的 Spetzler-Martin 分级为 2 级或更低。