Literature DB >> 27687326

Arterial complications of vascular Ehlers-Danlos syndrome.

Matthew J Eagleton1.   

Abstract

BACKGROUND: Vascular Ehlers-Danlos syndrome (EDS) is a relatively rare genetic syndrome that occurs owing to disorders in the metabolism of fibrillary collagen. These defects affect the soft connective tissues resulting in abnormalities in the skin, joints, hollow organs, and blood vessels. Patients with these defects frequently present at a young age with spontaneous arterial complications involving the medium-sized arteries. Complications involving the hollow organs, such as spontaneous colonic perforation, are observed as well. Given the fragility of the soft tissue, open and endovascular intervention on patients with vascular EDS is fraught with high complication rates.
METHODS: A PubMed search was performed to identify manuscripts published related to vascular EDS. This search included more than 747 articles. These findings were cross-referenced using key terms, including endovascular, embolization, surgery, genetics, pathophysiology, connective tissue disorders, vascular complications, systematic review, type III collagen, and COL3A1.
RESULTS: The references in key articles and review articles were evaluated for additional resources not identified in the PubMed search. Care must be taken to balance the risk of intervention vs the risk of continued observation. Life-threatening hemorrhage, however, mandates intervention.
CONCLUSIONS: With careful, altered approaches to tissue handling, endovascular approaches may provide a safer option for managing the arterial complications observed in patients with vascular EDS. Additional hope may also be found in the use of pharmacologic agents that reduce the incidence and severity of the arterial complications.
Copyright © 2016 Society for Vascular Surgery. Published by Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27687326     DOI: 10.1016/j.jvs.2016.06.120

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


  14 in total

1.  A multi-institutional experience in vascular Ehlers-Danlos syndrome diagnosis.

Authors:  Sherene Shalhub; Peter H Byers; Kelli L Hicks; Dawn M Coleman; Frank M Davis; Giovanni De Caridi; K Nicole Weaver; Erin M Miller; Marc L Schermerhorn; Katie Shean; Gustavo Oderich; Mauricio Ribeiro; Cole Nishikawa; Kristofer Charlton-Ouw; Christian-Alexander Behrendt; E Sebastian Debus; Yskert von Kodolitsch; Devin Zarkowsky; Richard J Powell; Melanie Pepin; Dianna M Milewicz; Ellen S Regalado; Peter F Lawrence; Karen Woo
Journal:  J Vasc Surg       Date:  2019-07-26       Impact factor: 4.268

Review 2.  Diagnostic approach and management of genetic aortopathies.

Authors:  Rohan Bhandari; Rajani D Aatre; Yogendra Kanthi
Journal:  Vasc Med       Date:  2020-02       Impact factor: 3.239

Review 3.  Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome.

Authors:  Josephina A N Meester; Aline Verstraeten; Dorien Schepers; Maaike Alaerts; Lut Van Laer; Bart L Loeys
Journal:  Ann Cardiothorac Surg       Date:  2017-11

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

Authors:  Sherene Shalhub; Peter H Byers; Kelli L Hicks; Kristofer Charlton-Ouw; Devin Zarkowsky; Dawn M Coleman; Frank M Davis; Ellen S Regalado; Giovanni De Caridi; K Nicole Weaver; Erin M Miller; Marc L Schermerhorn; Katie Shean; Gustavo Oderich; Mauricio Ribeiro; Cole Nishikawa; Christian-Alexander Behrendt; E Sebastian Debus; Yskert von Kodolitsch; Richard J Powell; Melanie Pepin; Dianna M Milewicz; Peter F Lawrence; Karen Woo
Journal:  J Vasc Surg       Date:  2019-05-21       Impact factor: 4.268

Review 5.  Type III collagen (COL3A1): Gene and protein structure, tissue distribution, and associated diseases.

Authors:  Helena Kuivaniemi; Gerard Tromp
Journal:  Gene       Date:  2019-05-07       Impact factor: 3.688

Review 6.  Dissecting the Heterogeneity of Human Thoracic Aortic Aneurysms Using Single-Cell Transcriptomics.

Authors:  Dogukan Mizrak; Hao Feng; Bo Yang
Journal:  Arterioscler Thromb Vasc Biol       Date:  2022-06-16       Impact factor: 10.514

Review 7.  Disorders of the Aorta and Aortic Valve in Connective Tissue Diseases.

Authors:  Bogna Grygiel-Górniak; Mary-Tiffany Oduah; Abdulbaril Olagunju; Michal Klokner
Journal:  Curr Cardiol Rep       Date:  2020-06-19       Impact factor: 2.931

8.  Arrhythmias and myocardial fragility in Ehlers-Danlos syndrome: Complications after routine ICD placement.

Authors:  Vinisha Garg; Malcolm Bersohn; Janet K Han
Journal:  HeartRhythm Case Rep       Date:  2018-04-05

9.  Vascular Ehlers-Danlos Syndrome with a Novel Missense Mutation in COL3A1: A Man in His 50s with Aortic Dissection after Interventional Treatment for Hemothorax as the First Manifestation.

Authors:  Kosuke Sakai; Maiko Toda; Hiroyuki Kyoyama; Hiroaki Nishimura; Akitoshi Kojima; Yoshiki Kuwabara; Yumiko Kobayashi; Satoshi Kikuchi; Yusuke Hirata; Gaku Moriyama; Wataru Watanabe; Koichi Akutsu; Maki Nakai; Takeshi Yamada; Akihiko Gemma; Kazutsugu Uematsu
Journal:  Intern Med       Date:  2019-08-06       Impact factor: 1.271

Review 10.  The Role of Cell Adhesion and Cytoskeleton Dynamics in the Pathogenesis of the Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders.

Authors:  Sabeeha Malek; Darius V Köster
Journal:  Front Cell Dev Biol       Date:  2021-04-21
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