CADISP-Genetics: An International Project Searching for Genetic Risk Factors of Cervical Artery Dissections

Author:

Debette S.1,Metso T. M.2,Pezzini A.3,Engelter S. T.4,Leys D.1,Lyrer P.4,Metso A. J.2,Brandt T.5,Kloss M.6,Lichy C.6,Hausser I.6,Touze E.7,Markus H. S.8,Abboud S.9,Caso V.10,Bersano A.11,Grau A.12,Altintas A.13,Amouyel P.14,Tatlisumak T.2,Dallongeville J.14,Grond-Ginsbach C.6,

Affiliation:

1. Department of Neurology, University Hospital of Lille, Lille, France

2. Department of Neurology, Helsinki University Central Hospital, Helsinki, Finland

3. Department of Neurology, University Hospital of Brescia, Brescia, Italy

4. Department of Neurology, University Hospital of Basel, Basel, Switzerland

5. Department of Neurology, Schmieder-Klinik Heidelberg, Heidelberg, Germany

6. Department of Neurology, University Hospital of Heidelberg, Heidelberg, Germany

7. Department of Neurology, Paris Descartes University Sainte-Anne Hospital, Paris, France

8. Department of Neurology, Saint-George's University of London, London, UK

9. Department of Neurology, Erasmus University Hospital of Brussels, Brussels, Belgium

10. Department of Neurology, University Hospital of Perugia, Perugia, Italy

11. Department of Neurology, University Hospital of Milano, Milano, Italy

12. Department of Neurology, Ludwigshafen Hospital, Ludwigshafen, Germany

13. Department of Neurology, University Hospital of Istanbul, Istanbul, Turkey

14. Inserm, U744, Pasteur Institute, Lille, France

Abstract

Background Cervical artery dissection (CAD) is a frequent cause of ischemic stroke, and occasionally death, in young adults. Several lines of evidence suggest a genetic predisposition to CAD. However, previous genetic studies have been inconclusive mainly due to insufficient numbers of patients. Our hypothesis is that CAD is a multifactorial disease caused by yet largely unidentified genetic variants and environmental factors, which may interact. Our aim is to identify genetic variants associated with an increased risk of CAD and possibly gene-environment interactions. Methods We organized a multinational European network, Cervical Artery Dissection and Ischemic Stroke Patients (CADISP), which aims at increasing our knowledge of the pathophysiological mechanisms of this disease in a large group of patients. Within this network, we are aiming to perform a de novo genetic association analysis using both a genome-wide and a candidate gene approach. For this purpose, DNA from approximately 1100 patients with CAD, and 2000 healthy controls is being collected. In addition, detailed clinical, laboratory, diagnostic, therapeutic, and outcome data are being collected from all participants applying predefined criteria and definitions in a standardized way. We are expecting to reach the above numbers of subjects by early 2009. Conclusions We present the strategy of a collaborative project searching for the genetic risk factors of CAD. The CADISP network will provide detailed and novel data on environmental risk factors and genetic susceptibility to CAD.

Publisher

SAGE Publications

Subject

Neurology

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