The differences in surgical long-term outcomes between Marfan syndrome and Loeys-Dietz syndrome

J Thorac Cardiovasc Surg. 2022 Jul;164(1):16-25.e2. doi: 10.1016/j.jtcvs.2020.07.089. Epub 2020 Aug 7.

Abstract

Objective: The aim of this study was to disclose the differences of surgical outcomes between Marfan syndrome with mutations in fibrillin-1 gene and Loeys-Dietz syndrome with mutations in transforming growth factor-beta receptor 1 and 2.

Methods: We reviewed 368 patients aged less than 50 years who underwent surgery for thoracic aortic diseases between 1988 and 2019, and enrolled 99 patients with Marfan syndrome (26.9%; 57 men, 33 ± 7.5 years) and 24 patients with Loeys-Dietz syndrome (6.5%; 13 men, 28 ± 11 years).

Results: Freedom from all causes of mortality was similar between the 2 groups (P = .40, log-rank). The cumulative incidence of reintervention was significantly lower in the Marfan syndrome group than in the Loeys-Dietz syndrome group (P = .016, Gray). The cumulative incidence of first aortic arch reoperation for aortic arch aneurysm was significantly lower in the Marfan syndrome group than in the Loeys-Dietz syndrome group (P < .001, Gray). The cumulative incidence of first aortic root reoperation for aortic root aneurysm (P = .57, Gray) and first descending aorta reoperation for descending aortic aneurysm (P = .76, Gray) was similar between the 2 groups. The cumulative incidence of aortic dissection after initial surgery was significantly lower in Marfan syndrome than in Loeys-Dietz syndrome (P = .0059, Gray).

Conclusions: Loeys-Dietz syndrome with mutations in transforming growth factor-beta receptor 1 and 2 revealed higher rates of reoperation, and more specifically the arch reoperation was higher in those with Loeys-Dietz syndrome than those with Marfan syndrome. Aggressive arch surgery in the initial operation on the proximal aorta is recommendable in Loeys-Dietz syndrome to avoid additional aortic events. In Marfan syndrome, this is controversial in patients without dissection because of a low possibility to expand.

Keywords: Loeys–Dietz syndrome; Marfan syndrome; fibrillin-1; reoparation; transforming growth factor-beta receptor.

MeSH terms

  • Adolescent
  • Adult
  • Aorta / surgery
  • Aortic Dissection*
  • Female
  • Humans
  • Loeys-Dietz Syndrome* / epidemiology
  • Loeys-Dietz Syndrome* / surgery
  • Male
  • Marfan Syndrome* / complications
  • Marfan Syndrome* / genetics
  • Marfan Syndrome* / surgery
  • Receptor, Transforming Growth Factor-beta Type I / genetics
  • Receptor, Transforming Growth Factor-beta Type II / genetics
  • Young Adult

Substances

  • Receptor, Transforming Growth Factor-beta Type I
  • Receptor, Transforming Growth Factor-beta Type II
  • TGFBR1 protein, human
  • TGFBR2 protein, human