Histologic differences between the ascending and descending aortas in young adults with fibrillin-1 mutations.


Journal

The Journal of thoracic and cardiovascular surgery
ISSN: 1097-685X
Titre abrégé: J Thorac Cardiovasc Surg
Pays: United States
ID NLM: 0376343

Informations de publication

Date de publication:
04 2020
Historique:
received: 11 04 2018
revised: 28 01 2019
accepted: 31 01 2019
pubmed: 25 3 2019
medline: 31 3 2020
entrez: 26 3 2019
Statut: ppublish

Résumé

This study aimed to review the clinical results of young adult patients with aortic disease associated with mutations in the fibrillin-1 gene (FBN1) and disclose the histologic differences between the ascending and descending aortas. Between 2012 and 2015, 94 patients aged less than 50 years underwent surgery for thoracic aortic diseases. Forty-two patients (44.7%) had FBN-1 mutations. Of these, 40 patients (42.5%) with surgical specimens for histologic evaluation were included in the study. With the histologic results including the specimen sampled at their previous operations, cystic medial necrosis was classified into 3 grades according to the degree of the cystic area. Thirty-nine patients (97.5%) had aortic root dilatation (Z ≥2), and 13 patients (32.5%) had ectopia lentis. Thirty-nine patients (97.5%) fulfilled the diagnostic criteria for Marfan syndrome. There were no in-hospital deaths. The majority (27/29: 93.1%) of the specimens of the ascending aorta revealed cystic medial necrosis pattern. With grade III being the most severe condition, these cases were classified into grade I (n = 2), grade II (n = 5), and grade III (n = 20). In contrast, only 6 specimens (6/17: 35.3%) of the descending aorta showed a cystic medial necrosis pattern that was classified into grade I (n = 2) and grade III (n = 4), (P < .00001). Fewer specimens of the descending aorta revealed cystic medial necrosis compared with those of the ascending aorta. This difference might influence the characteristic aortic disease in Marfan syndrome associated with FBN-1 mutations.

Identifiants

pubmed: 30905418
pii: S0022-5223(19)30361-7
doi: 10.1016/j.jtcvs.2019.01.126
pii:
doi:

Substances chimiques

Fibrillin-1 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1214-1220.e1

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2019 The American Association for Thoracic Surgery. Published by Elsevier Inc. All rights reserved.

Auteurs

Yoshimasa Seike (Y)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.

Kenji Minatoya (K)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan; Department of Cardiovascular Surgery, Graduate School of Medicine, Kyoto University, Shogoin, Sakyo-ku, Japan. Electronic address: minatoya@kuhp.kyoto-u.ac.jp.

Hitoshi Matsuda (H)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.

Hatsue Ishibashi-Ueda (H)

Department of Pathology, National Cerebral and Cardiovascular Center, Osaka, Japan.

Hiroko Morisaki (H)

Department of Genetics and Bioscience, National Cerebral and Cardiovascular Center, Osaka, Japan.

Takayuki Morisaki (T)

Department of Genetics and Bioscience, National Cerebral and Cardiovascular Center, Osaka, Japan.

Junjiro Kobayashi (J)

Department of Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Osaka, Japan.

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Classifications MeSH