Prevalence and characteristics of brain arteriovenous malformations in hereditary hemorrhagic telangiectasia: a systematic review and meta-analysis

被引:70
作者
Brinjikji, Waleed [1 ]
Iyer, Vivek N. [2 ]
Wood, Christopher R. [1 ]
Lanzino, Giuseppe [3 ]
机构
[1] Mayo Clin, Dept Radiol, 200 1st St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Pulm & Crit Care Med, Rochester, MN USA
[3] Mayo Clin, Dept Neurosurg, Rochester, MN USA
关键词
arteriovenous malformation; hereditary hemorrhagic telangiectasia; stroke; vascular disorders; ENDOVASCULAR TREATMENT; GENOTYPE; CHILDREN; MANIFESTATIONS; REGRESSION; MUTATIONS; FEATURES; RISK; ENG; HHT;
D O I
10.3171/2016.7.JNS16847
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 SpetzlerMartin grade for these lesions is 2 or less in nearly 90% of patients.
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页码:302 / 310
页数:9
相关论文
共 52 条
[1]   Screening for pulmonary and cerebral arteriovenous malformations in children with hereditary haemorrhagic telangiectasia [J].
Al-Saleh, S. ;
Mei-Zahav, M. ;
Faughnan, M. E. ;
MacLusky, I. B. ;
Carpenter, S. ;
Letarte, M. ;
Ratjen, F. .
EUROPEAN RESPIRATORY JOURNAL, 2009, 34 (04) :875-881
[2]  
Anderson JL, 2014, ANN NEUROL, V76, pS239
[3]  
[Anonymous], HEMATOL REP S1
[4]  
[Anonymous], HEMATOL REP
[5]  
[Anonymous], HEMATOL REP S
[6]  
[Anonymous], HEMATOL REP
[7]  
[Anonymous], STROKE
[8]  
[Anonymous], HEMATOL REP
[9]  
[Anonymous], HAEMATOLOGICA M REPO
[10]  
[Anonymous], AJNR AM J NEURORADIO