Literature DB >> 31126764

A multi-institutional experience in the aortic and arterial pathology in individuals with genetically confirmed vascular Ehlers-Danlos syndrome.

Sherene Shalhub1, Peter H Byers2, Kelli L Hicks3, Kristofer Charlton-Ouw4, Devin Zarkowsky5, Dawn M Coleman6, Frank M Davis6, Ellen S Regalado7, Giovanni De Caridi8, K Nicole Weaver9, Erin M Miller10, Marc L Schermerhorn11, Katie Shean11, Gustavo Oderich12, Mauricio Ribeiro13, Cole Nishikawa14, Christian-Alexander Behrendt15, E Sebastian Debus16, Yskert von Kodolitsch16, Richard J Powell17, Melanie Pepin2, Dianna M Milewicz7, Peter F Lawrence18, Karen Woo18.   

Abstract

OBJECTIVE: Vascular Ehlers-Danlos syndrome (vEDS) is a rare connective tissue disorder owing to pathogenic variants in COL3A1 that lead to impaired type III collagen production. We aim to describe the contemporary multi-institutional experience of aortic and arterial pathology in individuals with vEDS, to evaluate disease patterns and refine management recommendations.
METHODS: This cross-sectional, retrospective study of individuals with genetically confirmed vEDS was conducted between 2000 and 2015 at multiple institutions participating in the Vascular Low Frequency Disease Consortium. Aortic and arterial events including aneurysms, pseudoaneurysms, dissections, fistulae, or ruptures were studied. Demographics, COL3A1 variants, management, and outcomes data were collected and analyzed. Individuals with and without arterial events were compared.
RESULTS: Eleven institutions identified 86 individuals with pathogenic variants in COL3A1 (47.7% male, 86% Caucasian; median age, 41 years; interquartile range [IQR], 31.0-49.5 years; 65.1% missense COL3A1 variants). The median follow-up from the time of vEDS diagnosis was 7.5 years (IQR, 3.5-12.0 years). A total of 139 aortic/arterial pathologies were diagnosed in 53 individuals (61.6%; 50.9% male; 88.5% Caucasian; median age, 33 years; IQR, 25.0-42.3 years). The aortic/arterial events presented as an emergency in 52 cases (37.4%). The most commonly affected arteries were the mesenteric arteries (31.7%), followed by cerebrovascular (16.5%), iliac (16.5%), and renal arteries (12.2%). The most common management was medical management. When undertaken, the predominant endovascular interventions were arterial embolization of medium sized arteries (13.4%), followed by stenting (2.5%). Aortic pathology was noted in 17 individuals (32%; 58.8% male; 94.1% Caucasian; median age, 38.5 years; IQR, 30.8-44.7 years). Most notably, four individuals underwent successful abdominal aortic aneurysm repair with excellent results on follow-up. Individuals with missense mutations, in which glycine was substituted with a large amino acid, had an earlier onset of aortic/arterial pathology (median age, 30 years; IQR, 23.5-37 years) compared with the other pathogenic COL3A1 variants (median age, 36 years; IQR, 29.5-44.8 years; P = .065). There were 12 deaths (22.6%) at a median age of 36 years (IQR, 28-51 years).
CONCLUSIONS: Most of the vEDS arterial manifestations were managed medically in this cohort. When intervention is required for an enlarging aneurysm or rupture, embolization, and less frequently stenting, seem to be well-tolerated. Open repair of abdominal aortic aneurysm seems to be as well-tolerated as in those without vEDS; vEDS should not be a deterrent to offering an operation. Future work to elucidate the role of surgical interventions and refine management recommendations in the context of patient centered outcomes is warranted.
Copyright © 2019 Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Arterial aneurysm; Arterial dissection; Arterial rupture; COL3A1 mutation; Vascular Ehlers-Danlos syndrome

Mesh:

Substances:

Year:  2019        PMID: 31126764      PMCID: PMC8240141          DOI: 10.1016/j.jvs.2019.01.069

Source DB:  PubMed          Journal:  J Vasc Surg        ISSN: 0741-5214            Impact factor:   4.268


  28 in total

1.  Embolization of life-threatening arterial rupture in patients with vascular Ehlers-Danlos syndrome.

Authors:  Takuya Okada; Michael Frank; Olivier Pellerin; Massimiliano Di Primio; Georgios Angelopoulos; Marie-Fazia Boughenou; Jean-Yves Pagny; Emmanuel Messas; Marc Sapoval
Journal:  Cardiovasc Intervent Radiol       Date:  2013-05-09       Impact factor: 2.740

2.  Mutations in the COL3A1 gene result in the Ehlers-Danlos syndrome type IV and alterations in the size and distribution of the major collagen fibrils of the dermis.

Authors:  L T Smith; U Schwarze; J Goldstein; P H Byers
Journal:  J Invest Dermatol       Date:  1997-03       Impact factor: 8.551

3.  The type of variants at the COL3A1 gene associates with the phenotype and severity of vascular Ehlers-Danlos syndrome.

Authors:  Michael Frank; Juliette Albuisson; Brigitte Ranque; Lisa Golmard; Jean-Michael Mazzella; Laurence Bal-Theoleyre; Anne-Laure Fauret; Tristan Mirault; Nicolas Denarié; Elie Mousseaux; Pierre Boutouyrie; Jean-Noël Fiessinger; Joseph Emmerich; Emmanuel Messas; Xavier Jeunemaitre
Journal:  Eur J Hum Genet       Date:  2015-03-11       Impact factor: 4.246

4.  Endovascular thoracic aortic repair in confirmed or suspected genetically triggered thoracic aortic dissection.

Authors:  Sherene Shalhub; Kim A Eagle; Federico M Asch; Scott A LeMaire; Dianna M Milewicz
Journal:  J Vasc Surg       Date:  2018-03-19       Impact factor: 4.268

Review 5.  Treatment of spontaneous carotid-cavernous fistula in Ehlers-Danlos syndrome by transvenous occlusion with Guglielmi detachable coils. Case report and review of the literature.

Authors:  A A Kanner; S Maimon; Z H Rappaport
Journal:  J Neurosurg       Date:  2000-10       Impact factor: 5.115

6.  Splicing defects in the COL3A1 gene: marked preference for 5' (donor) spice-site mutations in patients with exon-skipping mutations and Ehlers-Danlos syndrome type IV.

Authors:  U Schwarze; J A Goldstein; P H Byers
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

7.  Effect of celiprolol on prevention of cardiovascular events in vascular Ehlers-Danlos syndrome: a prospective randomised, open, blinded-endpoints trial.

Authors:  Kim-Thanh Ong; Jérôme Perdu; Julie De Backer; Erwan Bozec; Patrick Collignon; Joseph Emmerich; Anne-Laure Fauret; Jean-Noël Fiessinger; Dominique P Germain; Gabriella Georgesco; Jean-Sebastien Hulot; Anne De Paepe; Henri Plauchu; Xavier Jeunemaitre; Stéphane Laurent; Pierre Boutouyrie
Journal:  Lancet       Date:  2010-09-07       Impact factor: 79.321

Review 8.  Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome.

Authors:  Peter H Byers; John Belmont; James Black; Julie De Backer; Michael Frank; Xavier Jeunemaitre; Diana Johnson; Melanie Pepin; Leema Robert; Lynn Sanders; Nigel Wheeldon
Journal:  Am J Med Genet C Semin Med Genet       Date:  2017-03       Impact factor: 3.908

9.  Desmopressin responsiveness in children with Ehlers-Danlos syndrome associated bleeding symptoms.

Authors:  Kelley J Mast; Mark E Nunes; Frederick B Ruymann; Bryce A Kerlin
Journal:  Br J Haematol       Date:  2008-11-19       Impact factor: 6.998

10.  Patients with Ehlers-Danlos syndrome type IV lack type III collagen.

Authors:  F M Pope; G R Martin; J R Lichtenstein; R Penttinen; B Gerson; D W Rowe; V A McKusick
Journal:  Proc Natl Acad Sci U S A       Date:  1975-04       Impact factor: 11.205

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  2 in total

1.  A Newly Discovered Genetic Disorder Associated With Life-Threatening Aortic Disease in a 6-Year-Old Boy.

Authors:  Mohanad Hamandi; Madison L Bolin; Joy Fan; Allison T Lanfear; Seth K Woolbert; Ronald D Baxter; J Michael DiMaio; William T Brinkman
Journal:  J Investig Med High Impact Case Rep       Date:  2020 Jan-Dec

2.  Mitral Valve Prolapse and Its Motley Crew-Syndromic Prevalence, Pathophysiology, and Progression of a Common Heart Condition.

Authors:  Jordan E Morningstar; Annah Nieman; Christina Wang; Tyler Beck; Andrew Harvey; Russell A Norris
Journal:  J Am Heart Assoc       Date:  2021-06-22       Impact factor: 5.501

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