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Targeted genetic analysis in a large cohort of familial and sporadic cases of aneurysm or dissection of the thoracic aorta

Research output: Contribution to journalArticle

  • Ruwan Weerakkody
  • David Ross
  • David A Parry
  • Bulat Ziganshin
  • Jana Vandrovcova
  • Piyush Gampawar
  • Abdulshakur Abdullah
  • Jennifer Biggs
  • Julia Dumfarth
  • Yousef Ibrahim
  • Colin Bicknell
  • Mark Field
  • John Elefteriades
  • Nick Cheshire
  • Timothy J Aitman

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Original languageEnglish
JournalGenetics in Medicine
Early online date15 Mar 2018
Publication statusE-pub ahead of print - 15 Mar 2018


Thoracic aortic aneurysm/aortic dissection (TAAD) is a disorder with highly variable age of onset and phenotype. We sought to determine the prevalence of pathogenic variants in TAAD-associated genes in a mixed cohort of sporadic and familial TAAD patients and identify relevant genotype–phenotype relationships.

We used a targeted polymerase chain reaction and next-generation sequencing–based panel for genetic analysis of 15 TAAD-associated genes in 1,025 unrelated TAAD cases.

We identified 49 pathogenic or likely pathogenic (P/LP) variants in 47 cases (4.9% of those successfully sequenced). Almost half of the variants were in nonsyndromic cases with no known family history of aortic disease. Twenty-five variants were within FBN1 and two patients were found to harbor two P/LP variants. Presence of a related syndrome, younger age at presentation, family history of aortic disease, and involvement of the ascending aorta increased the risk of carrying a P/LP variant.

Given the poor prognosis of TAAD that is undiagnosed prior to acute rupture or dissection, genetic analysis of both familial and sporadic cases of TAAD will lead to new diagnoses, more informed management, and possibly reduced mortality through earlier, preclinical diagnosis in genetically determined cases and their family members.

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