Literature DB >> 27767404

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

Waleed Brinjikji1, Vivek N Iyer2, Christopher P Wood1, Giuseppe Lanzino3.   

Abstract

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.

Entities:  

Keywords:  AVF = arteriovenous fistula; AVM = arteriovenous malformation; HHT = hereditary hemorrhagic telangiectasia; HHT1 = HHT Type 1; HHT2 = HHT Type 2; arteriovenous malformation; hereditary hemorrhagic telangiectasia; stroke; vascular disorders

Mesh:

Year:  2016        PMID: 27767404     DOI: 10.3171/2016.7.JNS16847

Source DB:  PubMed          Journal:  J Neurosurg        ISSN: 0022-3085            Impact factor:   5.115


  18 in total

1.  Basal Ganglia T1 Hyperintensity in Hereditary Hemorrhagic Telangiectasia.

Authors:  A Parvinian; V N Iyer; B S Pannu; D R Apala; C P Wood; W Brinjikji
Journal:  AJNR Am J Neuroradiol       Date:  2017-08-03       Impact factor: 3.825

Review 2.  Angioarchitecture of Hereditary Arteriovenous Malformations.

Authors:  Patricia E Burrows
Journal:  Semin Intervent Radiol       Date:  2017-09-11       Impact factor: 1.513

3.  Antithrombotic therapy and intracranial bleeding in subjects with sporadic brain arteriovenous malformations: preliminary results from a retrospective study.

Authors:  Carmelo Lucio Sturiale; Fabrizio Pignotti; Marzia Giordano; Angelo Porfidia; Alessio Albanese; Igor Giarretta; Alfredo Puca; Eleonora Gaetani; Sonia D'Arrigo; Ada Truma; Alessandro Olivi; Roberto Pola
Journal:  Intern Emerg Med       Date:  2018-07-30       Impact factor: 3.397

4.  Intradural spinal cord arteriovenous shunts in the pediatric population: natural history, endovascular management, and follow-up.

Authors:  Arturo Consoli; Stanislas Smajda; Johannes Trenkler; Michael Söderman; Georges Rodesch
Journal:  Childs Nerv Syst       Date:  2019-03-07       Impact factor: 1.475

Review 5.  Vis-à-vis: a focus on genetic features of cerebral cavernous malformations and brain arteriovenous malformations pathogenesis.

Authors:  Concetta Scimone; Luigi Donato; Silvia Marino; Concetta Alafaci; Rosalia D'Angelo; Antonina Sidoti
Journal:  Neurol Sci       Date:  2018-12-06       Impact factor: 3.307

Review 6.  Genetics of brain arteriovenous malformations and cerebral cavernous malformations.

Authors:  Hiroki Hongo; Satoru Miyawaki; Yu Teranishi; Daiichiro Ishigami; Kenta Ohara; Yu Sakai; Daisuke Shimada; Motoyuki Umekawa; Satoshi Koizumi; Hideaki Ono; Hirofumi Nakatomi; Nobuhito Saito
Journal:  J Hum Genet       Date:  2022-07-13       Impact factor: 3.755

Review 7.  Molecular and genetic mechanisms in brain arteriovenous malformations: new insights and future perspectives.

Authors:  Sandra Vetiska; Thomas Wälchli; Ivan Radovanovic; Moncef Berhouma
Journal:  Neurosurg Rev       Date:  2022-10-11       Impact factor: 2.800

8.  Prevalence of Intracranial Aneurysms in Hereditary Hemorrhagic Telangiectasia: Report from a Single Reference Center.

Authors:  M S Perez Akly; C Vazquez; C H Besada; M J Rodriguez; M F Conde; A R Cajal; V A Peuchot; D Dardik; M M Baccanelli; M M Serra
Journal:  AJNR Am J Neuroradiol       Date:  2022-05-19       Impact factor: 4.966

Review 9.  Maternal Genetic Disorders in Pregnancy.

Authors:  Sarah Harris; Neeta L Vora
Journal:  Obstet Gynecol Clin North Am       Date:  2018-06       Impact factor: 2.844

10.  Neonatal bilateral cerebral high flow fistulae leading to detection of a HHT-family carrier.

Authors:  Hortensia Alvarez; Muhammad H Niazi; Joshua Loewenstein; Carolyn S Quinsey
Journal:  Interv Neuroradiol       Date:  2020-12-22       Impact factor: 1.764

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.