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Multicenter Study
. 2016 Dec;9(6):548-558.
doi: 10.1161/CIRCGENETICS.116.001485. Epub 2016 Nov 21.

International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium)

Multicenter Study

International Registry of Patients Carrying TGFBR1 or TGFBR2 Mutations: Results of the MAC (Montalcino Aortic Consortium)

Guillaume Jondeau et al. Circ Cardiovasc Genet. 2016 Dec.

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 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.

Keywords: Marfan syndrome; acute aortic dissection gene; aneurysm; aortic disease; aortic dissection; aortic surgery; diagnostics; genetics; human; peripheral vascular disease; sex differences.

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Figures

Figure 1
Figure 1
Survival of the population: A : survival free of cardiovascular death (excluded cancer, septicemia, death of unknown cause). B: survival (all deaths included).
Figure 2
Figure 2
Survival free of vascular features: A: survival free of any vascular feature (including discovery of arterial or aortic aneurysm, surgery or dissection). B:survival free of vascular or aortic event (including surgery or dissection)
Figure 3
Figure 3
Survival free of any aortic event (surgery or dissection) in males compared to females. A population with a TGFBR1 mutation. B: population with a TGFBR2 mutation.
Figure 4
Figure 4
Relation between age and aortic diameter measured before or at the time of event on the ascending aorta. A: surgery or dissection. Dissec A: dissection type A, Preventive Surg: preventive surgery of the ascending aorta. TGFBR1 and TGFBR2 refer to the mutation. X is age in year, Y is last aortic diameter measured before or at the time of the event (mm). B: diameter of the ascending aorta (mm) in patients with type A aortic dissection, according to the sex (M males, F females) and the gene mutated (TGFBR1 and TGFBR2). Only patients with aortic measures performed at a maximum of 1 year prior to aortic dissection are displayed.

References

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