Brain arteriovenous malformations associated with hereditary hemorrhagic telangiectasia

Gene-phenotype correlations

Takeo Nishida, Marie E. Faughnan, Timo Krings, Murali Chakinala, James R Gossage, William L. Young, Helen Kim, Tony Pourmohamad, Katharine J. Henderson, Stacy D. Schrum, Melissa James, Nancy Quinnine, Aditya Bharatha, Karel G. terBrugge, Robert I. White

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disease with a wide spectrum of vascular malformations (VMs) involving multiple organs. Nine to 16% of patients with HHT harbor brain arteriovenous malformations (AVMs), which can cause intracranial hemorrhage (ICH). Our objective was to study clinical manifestations of brain AVMs in patients with HHT and correlate these with the specific gene mutated. We reviewed records of 171 patients with HHT and brain AVMs. A history of ICH was found in 27% (41/152) patients, with a mean age of 26±18 range, (0-68) years. All of patients with ICH were neurologically asymptomatic prior to ICH. Multiple brain AVMs were found in 23% (170/39) of patients on initial examination. Genetic test results were available in 109 (64%) patients. Mutations in ENG, ACVRL1, and SMAD4 were present in 75 (69%), 18 (17%), and 2 (2%), respectively. A history of ICH was reported in 24% of patients with an ENG mutation and 27% of patients with an ACVRL1 mutation, with a mean age of 26±16 (range, 2-50) and 18±21 (0-48) years, respectively. No statistically significant differences in age at first brain AVM diagnosis, prevalence of ICH history, age at ICH, or other manifestations of brain AVMs were observed among gene groups. In conclusion, no evidence for differences in brain AVM characteristics was observed among HHT gene groups, although we cannot exclude clinically important differences. Larger studies are needed to further guide brain AVM screening decisions in patients with HHT.

Original languageEnglish (US)
Pages (from-to)2829-2834
Number of pages6
JournalAmerican Journal of Medical Genetics, Part A
Volume158 A
Issue number11
DOIs
StatePublished - Nov 1 2012

Fingerprint

Hereditary Hemorrhagic Telangiectasia
Arteriovenous Malformations
Intracranial Hemorrhages
Phenotype
Brain
Genes
Mutation
Inborn Genetic Diseases
Vascular Malformations

Keywords

  • Brain arteriovenous malformation
  • Genotype
  • Hereditary hemorrhagic telangiectasia
  • Intracranial hemorrhage

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Brain arteriovenous malformations associated with hereditary hemorrhagic telangiectasia : Gene-phenotype correlations. / Nishida, Takeo; Faughnan, Marie E.; Krings, Timo; Chakinala, Murali; Gossage, James R; Young, William L.; Kim, Helen; Pourmohamad, Tony; Henderson, Katharine J.; Schrum, Stacy D.; James, Melissa; Quinnine, Nancy; Bharatha, Aditya; terBrugge, Karel G.; White, Robert I.

In: American Journal of Medical Genetics, Part A, Vol. 158 A, No. 11, 01.11.2012, p. 2829-2834.

Research output: Contribution to journalArticle

Nishida, T, Faughnan, ME, Krings, T, Chakinala, M, Gossage, JR, Young, WL, Kim, H, Pourmohamad, T, Henderson, KJ, Schrum, SD, James, M, Quinnine, N, Bharatha, A, terBrugge, KG & White, RI 2012, 'Brain arteriovenous malformations associated with hereditary hemorrhagic telangiectasia: Gene-phenotype correlations', American Journal of Medical Genetics, Part A, vol. 158 A, no. 11, pp. 2829-2834. https://doi.org/10.1002/ajmg.a.35622
Nishida, Takeo ; Faughnan, Marie E. ; Krings, Timo ; Chakinala, Murali ; Gossage, James R ; Young, William L. ; Kim, Helen ; Pourmohamad, Tony ; Henderson, Katharine J. ; Schrum, Stacy D. ; James, Melissa ; Quinnine, Nancy ; Bharatha, Aditya ; terBrugge, Karel G. ; White, Robert I. / Brain arteriovenous malformations associated with hereditary hemorrhagic telangiectasia : Gene-phenotype correlations. In: American Journal of Medical Genetics, Part A. 2012 ; Vol. 158 A, No. 11. pp. 2829-2834.
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abstract = "Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant genetic disease with a wide spectrum of vascular malformations (VMs) involving multiple organs. Nine to 16{\%} of patients with HHT harbor brain arteriovenous malformations (AVMs), which can cause intracranial hemorrhage (ICH). Our objective was to study clinical manifestations of brain AVMs in patients with HHT and correlate these with the specific gene mutated. We reviewed records of 171 patients with HHT and brain AVMs. A history of ICH was found in 27{\%} (41/152) patients, with a mean age of 26±18 range, (0-68) years. All of patients with ICH were neurologically asymptomatic prior to ICH. Multiple brain AVMs were found in 23{\%} (170/39) of patients on initial examination. Genetic test results were available in 109 (64{\%}) patients. Mutations in ENG, ACVRL1, and SMAD4 were present in 75 (69{\%}), 18 (17{\%}), and 2 (2{\%}), respectively. A history of ICH was reported in 24{\%} of patients with an ENG mutation and 27{\%} of patients with an ACVRL1 mutation, with a mean age of 26±16 (range, 2-50) and 18±21 (0-48) years, respectively. No statistically significant differences in age at first brain AVM diagnosis, prevalence of ICH history, age at ICH, or other manifestations of brain AVMs were observed among gene groups. In conclusion, no evidence for differences in brain AVM characteristics was observed among HHT gene groups, although we cannot exclude clinically important differences. Larger studies are needed to further guide brain AVM screening decisions in patients with HHT.",
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