SMAD3 pathogenic variants: Risk for thoracic aortic disease and associated complications from the Montalcino Aortic Consortium

Ellen M. Hostetler, Ellen S. Regalado, Dong Chuan Guo, Nadine Hanna, Pauline Arnaud, Laura Muiño-Mosquera, Bert Louis Callewaert, Kwanghyuk Lee, Suzanne M. Leal, Stephanie E. Wallace, Andrea L. Rideout, Sarah Dyack, Rajani D. Aatre, Catherine Boileau, Julie De Backer, Guillaume Jondeau, Dianna M. Milewicz

Résultat de recherche: Articleexamen par les pairs

49 Citations (Scopus)

Résumé

Background Pathogenic variants in SMAD3 cause thoracic aortic aneurysms and dissections, along with aneurysms and rupture of other arteries. Here, we examined differences in clinical presentation of aortic events (dissection or surgical repair of an aneurysm) with respect to age and variant type in an international cohort of individuals with SMAD3 variants. Methods Aortic status and events, vital status and clinical features were abstracted through retrospective review of medical records of 212 individuals with 51 unique SMAD3 variants, including haploinsufficiency (HI) and missense substitutions in the MH2 domain, as well as novel in-frame deletions and missense variants in the MH1 domain. Results Aortic events were documented in 37% of cases, with dissections accounting for 70% of events. The median age at first aortic event was significantly lower in individuals with SMAD3 MH2 missense variants than those with HI variants (42years vs 49 years; p=0.003), but there was no difference in frequency of aortic events by variant type. The cumulative risk of an aortic event was 50% at 54 years of age. No aortic events in childhood were observed. Conclusions SMAD3 pathogenic variants cause thoracic aortic aneurysms and dissections in the majority of individuals with variable age of onset and reduced penetrance. Of the covariates examined, the type of underlying SMAD3 variant was responsible for some of this variation. Later onset of aortic events and the absence of aortic events in children associated with SMAD3 variants support gene-specific management of this disorder.

Langue d'origineEnglish
Pages (de-à)252-260
Nombre de pages9
JournalJournal of Medical Genetics
Volume56
Numéro de publication4
DOI
Statut de publicationPublished - avr. 1 2019

Note bibliographique

Funding Information:
Funding the following provided funding for this study: national institutes of Health (rO1 Hl62594 and P01Hl110869-01), the John ritter research Foundation, genetic aortic Disorders association of canada, the temerty Family Fund, French Ministry of Health (PHrc aOM09093;aOM10108); French agency for research (anr-14-ce15-0012).

Publisher Copyright:
© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.

ASJC Scopus Subject Areas

  • Genetics
  • Genetics(clinical)

PubMed: MeSH publication types

  • Journal Article
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

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