Heritable Thoracic Aortic Disease

Definition

Heritable thoracic aortic disease (HTAD) is aortic aneurysm or dissection attributable to an inherited genetic predisposition — either syndromic (Marfan, Loeys-Dietz, vascular Ehlers-Danlos, Turner) or non-syndromic (familial, often with an identified variant in ACTA2, MYH11, MYLK, PRKG1, TGFBR1/2, SMAD3 or LOX). Its clinical importance is that the thresholds, growth rates and family obligations differ from sporadic disease, and that the specific gene changes the threshold. (sources/AD-AHA-2022, rating: very high)

Key Concepts

Why it is a separate category

Genetic testing and family screening

Thresholds by syndrome

Syndrome Repair threshold Class
Marfan Root ≥50 mm I/B
Marfan with additional risk features ≥45 mm IIa
Marfan, area/height ratio ≥10 cm²/m IIa
Loeys-Dietz, TGFBR1/2 or SMAD3 Root ≥45 mm; arch/descending/abdominal ≥45 mm (IIb) IIa
Loeys-Dietz, TGFB2/3 ≥45 mm before pregnancy IIa
Non-syndromic HTAD, no identified gene Gene/diameter guided by affected relatives' event diameters; ~45 mm where that information is unavailable and there are high-risk features I–IIa
ACTA2 ~45 mm (lower, ~42 mm, with risk features) IIa/IIb
PRKG1 ~42 mm (~40 mm with risk features) IIb
Turner syndrome ASI ≥2.5 cm/m² plus risk factors IIa
Vascular Ehlers-Danlos Individualised — tissue fragility dominates; celiprolol first, surgery deferred IIa

Medical therapy

Surveillance

Pregnancy

Activity and counselling

Contradictions / Open Questions

Connections

Sources