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Multiple Arterial Dissections and Connective Tissue Abnormalities

Background: Although patients with multiple arterial dissections in distinct arterial regions rarely present with known connective tissue syndromes, we hypothesized that mild connective tissue abnormalities are common findings in these patients. Methods: From a consecutive register of 322 patients w...

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Autores principales: Erhart, Philipp, Körfer, Daniel, Dihlmann, Susanne, Qiao, Jia-Lu, Hausser, Ingrid, Ringleb, Peter, Männer, Jörg, Dikow, Nicola, Schaaf, Christian P., Grond-Ginsbach, Caspar, Böckler, Dittmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224905/
https://www.ncbi.nlm.nih.gov/pubmed/35743335
http://dx.doi.org/10.3390/jcm11123264
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author Erhart, Philipp
Körfer, Daniel
Dihlmann, Susanne
Qiao, Jia-Lu
Hausser, Ingrid
Ringleb, Peter
Männer, Jörg
Dikow, Nicola
Schaaf, Christian P.
Grond-Ginsbach, Caspar
Böckler, Dittmar
author_facet Erhart, Philipp
Körfer, Daniel
Dihlmann, Susanne
Qiao, Jia-Lu
Hausser, Ingrid
Ringleb, Peter
Männer, Jörg
Dikow, Nicola
Schaaf, Christian P.
Grond-Ginsbach, Caspar
Böckler, Dittmar
author_sort Erhart, Philipp
collection PubMed
description Background: Although patients with multiple arterial dissections in distinct arterial regions rarely present with known connective tissue syndromes, we hypothesized that mild connective tissue abnormalities are common findings in these patients. Methods: From a consecutive register of 322 patients with cervical artery dissection (CeAD), we identified and analyzed 4 patients with a history of additional dissections in other vascular beds. In three patients, dermal connective tissue was examined by electron microscopy. DNA from all four patients was studied by whole-exome sequencing and copy number variation (CNV) analysis. Results: The collagen fibers of dermal biopsies were pathologic in all three analyzed patients. One patient carried a CNV disrupting the COL3A1 and COL5A2 genes (vascular or hypermobility type of Ehlers–Danlos syndrome), and another patient a CNV in MYH11 (familial thoracic aortic aneurysms and dissections). The third patient carried a missense substitution in COL5A2. Conclusion: Three patients showed morphologic alterations of the dermal connective tissue, and two patients carried pathogenic variants in genes associated with arterial connective tissue dysfunction. The findings suggest that genetic testing should be recommended after recurrent arterial dissections, independently of apparent phenotypical signs of connective tissue disorders.
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spelling pubmed-92249052022-06-24 Multiple Arterial Dissections and Connective Tissue Abnormalities Erhart, Philipp Körfer, Daniel Dihlmann, Susanne Qiao, Jia-Lu Hausser, Ingrid Ringleb, Peter Männer, Jörg Dikow, Nicola Schaaf, Christian P. Grond-Ginsbach, Caspar Böckler, Dittmar J Clin Med Article Background: Although patients with multiple arterial dissections in distinct arterial regions rarely present with known connective tissue syndromes, we hypothesized that mild connective tissue abnormalities are common findings in these patients. Methods: From a consecutive register of 322 patients with cervical artery dissection (CeAD), we identified and analyzed 4 patients with a history of additional dissections in other vascular beds. In three patients, dermal connective tissue was examined by electron microscopy. DNA from all four patients was studied by whole-exome sequencing and copy number variation (CNV) analysis. Results: The collagen fibers of dermal biopsies were pathologic in all three analyzed patients. One patient carried a CNV disrupting the COL3A1 and COL5A2 genes (vascular or hypermobility type of Ehlers–Danlos syndrome), and another patient a CNV in MYH11 (familial thoracic aortic aneurysms and dissections). The third patient carried a missense substitution in COL5A2. Conclusion: Three patients showed morphologic alterations of the dermal connective tissue, and two patients carried pathogenic variants in genes associated with arterial connective tissue dysfunction. The findings suggest that genetic testing should be recommended after recurrent arterial dissections, independently of apparent phenotypical signs of connective tissue disorders. MDPI 2022-06-07 /pmc/articles/PMC9224905/ /pubmed/35743335 http://dx.doi.org/10.3390/jcm11123264 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Erhart, Philipp
Körfer, Daniel
Dihlmann, Susanne
Qiao, Jia-Lu
Hausser, Ingrid
Ringleb, Peter
Männer, Jörg
Dikow, Nicola
Schaaf, Christian P.
Grond-Ginsbach, Caspar
Böckler, Dittmar
Multiple Arterial Dissections and Connective Tissue Abnormalities
title Multiple Arterial Dissections and Connective Tissue Abnormalities
title_full Multiple Arterial Dissections and Connective Tissue Abnormalities
title_fullStr Multiple Arterial Dissections and Connective Tissue Abnormalities
title_full_unstemmed Multiple Arterial Dissections and Connective Tissue Abnormalities
title_short Multiple Arterial Dissections and Connective Tissue Abnormalities
title_sort multiple arterial dissections and connective tissue abnormalities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224905/
https://www.ncbi.nlm.nih.gov/pubmed/35743335
http://dx.doi.org/10.3390/jcm11123264
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