Literature DB >> 24922459

Survival is affected by mutation type and molecular mechanism in vascular Ehlers-Danlos syndrome (EDS type IV).

Melanie G Pepin1, Ulrike Schwarze1, Kenneth M Rice2, Mingdong Liu2, Dru Leistritz1, Peter H Byers3.   

Abstract

PURPOSE: We sought to characterize the natural history of vascular Ehlers-Danlos syndrome in individuals with heterozygous COL3A1 mutations.
METHODS: We reviewed clinical records for details of vascular, bowel, and organ complications in 1,231 individuals (630 index cases and 601 relatives).
RESULTS: Missense and splice-site mutations accounted for more than 90% of the 572 alterations that we had identified in COL3A1. Median survival was 51 years but was influenced by gender (lower in men) and by the type of mutation.
CONCLUSION: Although vascular Ehlers-Danlos syndrome appears to be genetically homogeneous, allelic heterogeneity is marked, and the natural history varies with gender and type of mutation in COL3A1. These findings indicate that when counseling families, confirmation of the presence of a COL3A1 mutation and its nature can help evaluate the risks of complications. These data are also important ingredients in both the selection and allocation of individuals to appropriate arms in clinical trials to assess the effects of interventions.

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Year:  2014        PMID: 24922459     DOI: 10.1038/gim.2014.72

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  58 in total

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Journal:  Cardiovasc Diagn Ther       Date:  2018-12

4.  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
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Authors:  Philipp Karschnia; Sayoko Nishimura; Angeliki Louvi
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Review 7.  Cerebral microhemorrhages: mechanisms, consequences, and prevention.

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8.  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
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9.  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
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Review 10.  Genes Associated with Thoracic Aortic Aneurysm and Dissection: An Update and Clinical Implications.

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Journal:  Aorta (Stamford)       Date:  2017-02-01
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