International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium). (December 2016)
- Record Type:
- Journal Article
- Title:
- International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium). (December 2016)
- Main Title:
- International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations
- Authors:
- Jondeau, Guillaume
Ropers, Jacques
Regalado, Ellen
Braverman, Alan
Evangelista, Arturo
Teixedo, Guisela
De Backer, Julie
Muiño-Mosquera, Laura
Naudion, Sophie
Zordan, Cecile
Morisaki, Takayuki
Morisaki, Hiroto
Von Kodolitsch, Yskert
Dupuis-Girod, Sophie
Morris, Shaine A.
Jeremy, Richmond
Odent, Sylvie
Adès, Leslie C.
Bakshi, Madhura
Holman, Katherine
LeMaire, Scott
Milleron, Olivier
Langeois, Maud
Spentchian, Myrtille
Aubart, Melodie
Boileau, Catherine
Pyeritz, Reed
Milewicz, Dianna M. - Abstract:
- Abstract : Background—: The natural history of aortic diseases in patients with TGFBR1 or TGFBR2 mutations reported by different investigators has varied greatly. In particular, the current recommendations for the timing of surgical repair of the aortic root aneurysms may be overly aggressive. Methods and Results—: The Montalcino Aortic Consortium, which includes 15 centers worldwide that specialize in heritable thoracic aortic diseases, was used to gather data on 441 patients from 228 families, with 176 cases harboring a mutation in TGBR1 and 265 in TGFBR2 . Patients harboring a TGFBR1 mutation have similar survival rates (80% survival at 60 years), aortic risk (23% aortic dissection and 18% preventive aortic surgery), and prevalence of extra-aortic features (29% hypertelorism, 53% cervical arterial tortuosity, and 27% wide scars) when compared with patients harboring a TGFBR2 mutation. However, TGFBR1 males had a greater aortic risk than females, whereas TGFBR2 males and females had a similar aortic risk. Additionally, aortic root diameter prior to or at the time of type A aortic dissection tended to be smaller in patients carrying a TGFBR2 mutation and was ⩽45 mm in 6 women with TGFBR2 mutations, presenting with marked systemic features and low body surface area. Aortic dissection was observed in 1.6% of pregnancies. Conclusions—: Patients with TGFBR1 or TGFBR2 mutations show the same prevalence of systemic features and the same global survival. Preventive aortic surgeryAbstract : Background—: The natural history of aortic diseases in patients with TGFBR1 or TGFBR2 mutations reported by different investigators has varied greatly. In particular, the current recommendations for the timing of surgical repair of the aortic root aneurysms may be overly aggressive. Methods and Results—: The Montalcino Aortic Consortium, which includes 15 centers worldwide that specialize in heritable thoracic aortic diseases, was used to gather data on 441 patients from 228 families, with 176 cases harboring a mutation in TGBR1 and 265 in TGFBR2 . Patients harboring a TGFBR1 mutation have similar survival rates (80% survival at 60 years), aortic risk (23% aortic dissection and 18% preventive aortic surgery), and prevalence of extra-aortic features (29% hypertelorism, 53% cervical arterial tortuosity, and 27% wide scars) when compared with patients harboring a TGFBR2 mutation. However, TGFBR1 males had a greater aortic risk than females, whereas TGFBR2 males and females had a similar aortic risk. Additionally, aortic root diameter prior to or at the time of type A aortic dissection tended to be smaller in patients carrying a TGFBR2 mutation and was ⩽45 mm in 6 women with TGFBR2 mutations, presenting with marked systemic features and low body surface area. Aortic dissection was observed in 1.6% of pregnancies. Conclusions—: Patients with TGFBR1 or TGFBR2 mutations show the same prevalence of systemic features and the same global survival. Preventive aortic surgery at a diameter of 45 mm, lowered toward 40 in females with low body surface area, TGFBR2 mutation, and severe extra-aortic features may be considered. Abstract : Supplemental Digital Content is available in the text. … (more)
- Is Part Of:
- Circulation. Volume 9:Number 6(2016)
- Journal:
- Circulation
- Issue:
- Volume 9:Number 6(2016)
- Issue Display:
- Volume 9, Issue 6 (2016)
- Year:
- 2016
- Volume:
- 9
- Issue:
- 6
- Issue Sort Value:
- 2016-0009-0006-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-12
- Subjects:
- acute aortic dissection gene -- aneurysm -- aortic disease -- aortic dissection -- aortic surgery -- diagnostics -- genetics -- human -- Marfan syndrome -- peripheral vascular disease -- sex differences
Arrhythmia -- Periodicals
Heart -- Electric properties -- Periodicals
616.1042 - Journal URLs:
- http://gateway.ovid.com/ovidweb.cgi?T=JS&MODE=ovid&PAGE=toc&D=ovft&AN=01337497-000000000-00000 ↗
http://journals.lww.com ↗ - DOI:
- 10.1161/CIRCGENETICS.116.001485 ↗
- Languages:
- English
- ISSNs:
- 1942-325X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3265.262520
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 2309.xml