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Prevalence and Complications of Aberrant Subclavian Artery in Patients With Heritable and Nonheritable Arteriopathies.
Giuliani, Lorenzo; Di Toro, Alessandro; Urtis, Mario; Narula, Nupoor; Grasso, Maurizia; Pelenghi, Stefano; Belliato, Mirko; Bozzani, Antonio; Arici, Vittorio; Pellegrini, Carlo; Serio, Alessandra; Pilotto, Andrea; Fergnani, Viola; Antoniazzi, Elena; Magrassi, Lorenzo; Dore, Roberto; Valentini, Adele; Preda, Lorenzo; Calliada, Fabrizio; Quaretti, Pietro; Pirrelli, Stefano; Kodama, Takaide; Vricella, Luca; Cameron, Duke; Arbustini, Eloisa.
Afiliação
  • Giuliani L; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy.
  • Di Toro A; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy.
  • Urtis M; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy.
  • Narula N; Division of Cardiology and Weill Cornell Women's Heart Program, Weill Cornell Medicine, New York, New York, USA.
  • Grasso M; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy.
  • Pelenghi S; Cardiac 1 Surgery Unit, Cardiothorax and Vascular Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Belliato M; AR2-Cardiothoracic ICU, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Bozzani A; Vascular and Endovascular Surgery Unit, Department of Surgical Science, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Arici V; Vascular and Endovascular Surgery Unit, Department of Surgical Science, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Pellegrini C; Cardiac 1 Surgery Unit, Cardiothorax and Vascular Department, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy; Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, Università degli Studi di Pavia, Pavia, Italy.
  • Serio A; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy.
  • Pilotto A; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy.
  • Fergnani V; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy.
  • Antoniazzi E; Ophthalmology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Magrassi L; Neurosurgery, Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, Università degli Studi di Pavia, Pavia, Italy.
  • Dore R; Unit of Radiology, Clinical Institute, Città di Pavia, Pavia, Italy.
  • Valentini A; Department of Radiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Preda L; Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, Università degli Studi di Pavia, Pavia, Italy; Department of Radiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Calliada F; Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, Università degli Studi di Pavia, Pavia, Italy.
  • Quaretti P; Unit of Interventional Radiology-Department of Radiology, Fondazione IRCCS Policlinico San Matteo, Pavia, Italy.
  • Pirrelli S; Division of Vascular Surgery-Cardiovascular Department, ASST Papa Giovanni XXIII, Bergamo, Italy.
  • Kodama T; Department of Cardiology, Toranomon Hospital, Tokyo, Japan.
  • Vricella L; The Heart Institute for Children, Advocate Children's Hospital, Oak Lawn, Illinois, USA; Department of Surgery, University of Chicago Medicine, Chicago, Illinois, USA.
  • Cameron D; Division of Cardiac Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, USA.
  • Arbustini E; Transplant Research Area and Centre for Inherited Cardiovascular Diseases, Fondazione IRCCS Policlinico San Matteo, VASCERN HTAD European Reference Centre, Pavia, Italy. Electronic address: e.arbustini@smatteo.pv.it.
J Am Coll Cardiol ; 81(10): 979-991, 2023 03 14.
Article em En | MEDLINE | ID: mdl-36889877
ABSTRACT

BACKGROUND:

An aberrant subclavian artery (ASA) (or lusoria) is the most common congenital anomaly of the aortic arch (0.5%-2.2%; female-to-male ratio 21 to 31). ASA can become aneurysmal and result in dissection, involving Kommerell's diverticulum when present and the aorta. Data of its significance in genetic arteriopathies are not available.

OBJECTIVES:

The purpose of this study was to assess the prevalence and complications of ASA in gene-positive and -negative nonatherosclerotic arteriopathies. MATERIALS The series includes 1,418 consecutive patients with gene-positive (n = 854) and gene-negative arteriopathies (n = 564) diagnosed as part of institutional work-up for nonatherosclerotic syndromic and nonsyndromic arteriopathies. Comprehensive evaluation includes genetic counseling, next-generation sequencing multigene testing, cardiovascular and multidisciplinary assessment, and whole-body computed tomography angiography.

RESULTS:

ASA was found in 34 of 1,418 cases (2.4%), with a similar prevalence in gene-positive (n = 21 of 854, 2.5%) and gene-negative (n = 13 of 564, 2.3%) arteriopathies. Of the former 21 patients, 14 had Marfan syndrome, 5 had Loeys-Dietz syndrome, 1 had type-IV Ehlers-Danlos syndrome, and 1 had periventricular heterotopia type 1. ASA did not segregate with genetic defects. Dissection occurred in 5 of 21 patients with genetic arteriopathies (23.8%; 2 Marfan syndrome and 3 Loeys-Dietz syndrome), all with associated Kommerell's diverticulum. No dissections occurred in gene-negative patients. At baseline, none of the 5 patients with ASA dissection fulfilled criteria for elective repair according to guidelines.

CONCLUSIONS:

The risk of complications of ASA is higher in patients with genetic arteriopathies and is difficult to predict. In these diseases, imaging of the supra-aortic trunks should enter baseline investigations. Determination of precise indications for repair can prevent unexpected acute events such as those described.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Divertículo / Síndrome de Loeys-Dietz / Cardiopatias Congênitas / Síndrome de Marfan Tipo de estudo: Guideline / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Vasculares / Divertículo / Síndrome de Loeys-Dietz / Cardiopatias Congênitas / Síndrome de Marfan Tipo de estudo: Guideline / Prevalence_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article