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November 25, 2014; 83 (22) Article

Familial occurrence and heritable connective tissue disorders in cervical artery dissection

Stéphanie Debette, Barbara Goeggel Simonetti, Sabrina Schilling, Juan José Martin, Manja Kloss, Hakan Sarikaya, Ingrid Hausser, Stefan Engelter, Tiina M. Metso, Alessandro Pezzini, Vincent Thijs, Emmanuel Touzé, Stefano Paolucci, Paolo Costa, Maria Sessa, Yves Samson, Yannick Béjot, Ayse Altintas, Antti J. Metso, Dominique Hervé, Christoph Lichy, Simon Jung, Urs Fischer, Chantal Lamy, Armin Grau, Hugues Chabriat, Valeria Caso, Philippe A. Lyrer, Christian Stapf, Turgut Tatlisumak, Tobias Brandt, Elisabeth Tournier-Lasserve, Dominique P. Germain, Michael Frank, Ralf W. Baumgartner, Caspar Grond-Ginsbach, Marie-Germaine Bousser, Didier Leys, Jean Dallongeville, Anna Bersano, Marcel Arnold, For the CADISP-plus consortium
First published October 29, 2014, DOI: https://doi.org/10.1212/WNL.0000000000001027
Stéphanie Debette
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Barbara Goeggel Simonetti
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Sabrina Schilling
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Juan José Martin
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Manja Kloss
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Hakan Sarikaya
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Ingrid Hausser
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Stefan Engelter
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Tiina M. Metso
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Alessandro Pezzini
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Vincent Thijs
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Emmanuel Touzé
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Stefano Paolucci
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Paolo Costa
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Maria Sessa
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Yves Samson
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Yannick Béjot
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Ayse Altintas
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Antti J. Metso
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Dominique Hervé
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Christoph Lichy
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Simon Jung
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Urs Fischer
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Chantal Lamy
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Armin Grau
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Hugues Chabriat
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Valeria Caso
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Philippe A. Lyrer
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Christian Stapf
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Turgut Tatlisumak
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Tobias Brandt
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Elisabeth Tournier-Lasserve
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Dominique P. Germain
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Michael Frank
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Ralf W. Baumgartner
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Caspar Grond-Ginsbach
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Marie-Germaine Bousser
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Didier Leys
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Jean Dallongeville
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Anna Bersano
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Marcel Arnold
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Familial occurrence and heritable connective tissue disorders in cervical artery dissection
Stéphanie Debette, Barbara Goeggel Simonetti, Sabrina Schilling, Juan José Martin, Manja Kloss, Hakan Sarikaya, Ingrid Hausser, Stefan Engelter, Tiina M. Metso, Alessandro Pezzini, Vincent Thijs, Emmanuel Touzé, Stefano Paolucci, Paolo Costa, Maria Sessa, Yves Samson, Yannick Béjot, Ayse Altintas, Antti J. Metso, Dominique Hervé, Christoph Lichy, Simon Jung, Urs Fischer, Chantal Lamy, Armin Grau, Hugues Chabriat, Valeria Caso, Philippe A. Lyrer, Christian Stapf, Turgut Tatlisumak, Tobias Brandt, Elisabeth Tournier-Lasserve, Dominique P. Germain, Michael Frank, Ralf W. Baumgartner, Caspar Grond-Ginsbach, Marie-Germaine Bousser, Didier Leys, Jean Dallongeville, Anna Bersano, Marcel Arnold, For the CADISP-plus consortium
Neurology Nov 2014, 83 (22) 2023-2031; DOI: 10.1212/WNL.0000000000001027

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This article has a correction. Please see:

  • Familial occurrence and heritable connective tissue disorders in cervical artery dissection - December 06, 2016
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Abstract

Objective: In a large series of patients with cervical artery dissection (CeAD), a major cause of ischemic stroke in young and middle-aged adults, we aimed to examine frequencies and correlates of family history of CeAD and of inherited connective tissue disorders.

Methods: We combined data from 2 large international multicenter cohorts of consecutive patients with CeAD in 23 neurologic departments participating in the CADISP-plus consortium, following a standardized protocol. Frequency of reported family history of CeAD and of inherited connective tissue disorders was assessed. Putative risk factors, baseline features, and 3-month outcome were compared between groups.

Results: Among 1,934 consecutive patients with CeAD, 20 patients (1.0%, 95% confidence interval: 0.6%–1.5%) from 17 families (0.9%, 0.5%–1.3%) had a family history of CeAD. Family history of CeAD was significantly more frequent in patients with carotid location of the dissection and elevated cholesterol levels. Two patients without a family history of CeAD had vascular Ehlers-Danlos syndrome with a mutation in COL3A1. This diagnosis was suspected in 2 additional patients, but COL3A1 sequencing was negative. Two patients were diagnosed with classic and hypermobile Ehlers-Danlos syndrome, one patient with Marfan syndrome, and one with osteogenesis imperfecta, based on clinical criteria only.

Conclusions: In this largest series of patients with CeAD to date, family history of symptomatic CeAD was rare and inherited connective tissue disorders seemed exceptional. This finding supports the notion that CeAD is a multifactorial disease in the vast majority of cases.

GLOSSARY

CADISP=
Cervical Artery Dissection and Ischemic Stroke Patients;
CeAD=
cervical artery dissection;
CI=
confidence interval;
CTD=
connective tissue disorder;
EDS=
Ehlers-Danlos syndrome;
vEDS=
vascular Ehlers-Danlos syndrome

Footnotes

  • ↵* These authors contributed equally to this work.

  • ↵‡ These authors jointly directed this work.

  • CADISP-plus consortium coinvestigators are listed on the Neurology® Web site at Neurology.org.

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Supplemental data at Neurology.org

  • Received March 10, 2014.
  • Accepted in final form August 26, 2014.
  • © 2014 American Academy of Neurology
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