Coarctation of Aorta With Tricuspid Aortic Valve Is Not Associated With Ascending Aortic Aneurysm.

bicuspid aortic valve coarctation of aorta thoracic aorta aneurysms

Journal

Journal of the American College of Cardiology
ISSN: 1558-3597
Titre abrégé: J Am Coll Cardiol
Pays: United States
ID NLM: 8301365

Informations de publication

Date de publication:
26 Mar 2024
Historique:
received: 11 10 2023
revised: 05 01 2024
accepted: 29 01 2024
medline: 21 3 2024
pubmed: 21 3 2024
entrez: 20 3 2024
Statut: ppublish

Résumé

Aortic aneurysm is common in patients with coarctation of aorta (COA), but it is unclear whether the risk of aortic aneurysms is due to COA or related to the presence of other risk factors such as bicuspid aortic valve (BAV) and hypertension. The purpose of this study was to assess the relationship among COA, BAV, and thoracic aortic aneurysms. A total of 867 patients with COA (COA group) were matched 1:1:1 to 867 patients with isolated BAV (BAV group) and 867 patients without structural heart disease (SHD) (no-SHD group). The COA group was further subdivided into a COA+BAV subgroup (n = 304 [35%]), and COA with tricuspid aortic valve (TAV) (COA+TAV subgroup [n = 563 (65%)]). Aortic dimensions were assessed at baseline and at 3, 5, and 7 years. Compared with the no-SHD group, the COA+BAV subgroup had larger aortic root diameter (37 mm [Q1-Q3: 30-43 mm] vs 32 mm [Q1-Q3: 27-35 mm]; P < 0.001) and mid ascending aorta dimeter (34 mm [Q1-Q3: 29-40 mm] vs 28 mm [Q1-Q3: 24-31 mm]; P = 0.008). Similarly, the BAV group had larger aortic root diameter (37 mm [Q1-Q3: 30-42 mm] vs 32 mm [Q1-Q3: 27-35 mm]; P < 0.001), and mid ascending aorta dimeter (35 mm [Q1-Q3: 30-40 mm] vs 28 mm [Q1-Q3: 24-31 mm]; P < 0.001). Compared with the COA+TAV subgroup, the COA+BAV subgroup and BAV group were associated with larger aortic root and mid ascending aorta diameter at baseline and follow-up. The risk of acute aortic complications was low in all groups. These findings suggest that BAV (and not COA) was associated with ascending thoracic aorta dimensions, and that patients with COA+TAV were not at a greater risk of developing ascending aortic aneurysms as compared with patients without SHD.

Sections du résumé

BACKGROUND BACKGROUND
Aortic aneurysm is common in patients with coarctation of aorta (COA), but it is unclear whether the risk of aortic aneurysms is due to COA or related to the presence of other risk factors such as bicuspid aortic valve (BAV) and hypertension.
OBJECTIVES OBJECTIVE
The purpose of this study was to assess the relationship among COA, BAV, and thoracic aortic aneurysms.
METHODS METHODS
A total of 867 patients with COA (COA group) were matched 1:1:1 to 867 patients with isolated BAV (BAV group) and 867 patients without structural heart disease (SHD) (no-SHD group). The COA group was further subdivided into a COA+BAV subgroup (n = 304 [35%]), and COA with tricuspid aortic valve (TAV) (COA+TAV subgroup [n = 563 (65%)]). Aortic dimensions were assessed at baseline and at 3, 5, and 7 years.
RESULTS RESULTS
Compared with the no-SHD group, the COA+BAV subgroup had larger aortic root diameter (37 mm [Q1-Q3: 30-43 mm] vs 32 mm [Q1-Q3: 27-35 mm]; P < 0.001) and mid ascending aorta dimeter (34 mm [Q1-Q3: 29-40 mm] vs 28 mm [Q1-Q3: 24-31 mm]; P = 0.008). Similarly, the BAV group had larger aortic root diameter (37 mm [Q1-Q3: 30-42 mm] vs 32 mm [Q1-Q3: 27-35 mm]; P < 0.001), and mid ascending aorta dimeter (35 mm [Q1-Q3: 30-40 mm] vs 28 mm [Q1-Q3: 24-31 mm]; P < 0.001). Compared with the COA+TAV subgroup, the COA+BAV subgroup and BAV group were associated with larger aortic root and mid ascending aorta diameter at baseline and follow-up. The risk of acute aortic complications was low in all groups.
CONCLUSIONS CONCLUSIONS
These findings suggest that BAV (and not COA) was associated with ascending thoracic aorta dimensions, and that patients with COA+TAV were not at a greater risk of developing ascending aortic aneurysms as compared with patients without SHD.

Identifiants

pubmed: 38508846
pii: S0735-1097(24)00230-4
doi: 10.1016/j.jacc.2024.01.026
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1136-1146

Informations de copyright

Copyright © 2024 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Funding Support and Author Disclosures The MACHD registry is supported by the Al-Bahar Research grant. Dr Egbe is supported by National Heart, Lung, and Blood Institute grants (R01 HL158517, R01 HL160761, and R01 HL162830). All other authors have reported that they have no relationships relevant to the contents of this paper to disclose.

Auteurs

Alexander C Egbe (AC)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA. Electronic address: egbe.alexander@mayo.edu.

William R Miranda (WR)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA.

Omar Abozied (O)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA.

C Charles Jain (CC)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA.

Luke J Burchill (LJ)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA.

Snigdha Karnakoti (S)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA.

Marwan H Ahmed (MH)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA.

Christopher J Francois (CJ)

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Heidi M Connolly (HM)

Department of Cardiovascular Medicine Mayo Clinic, Rochester, Minnesota, USA.

Classifications MeSH