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

التفاصيل البيبلوغرافية
العنوان: CADISP-Genetics: An International Project Searching for Genetic Risk Factors of Cervical Artery Dissections
المؤلفون: S, Debette, T M, Metso, A, Pezzini, S T, Engelter, D, Leys, P, Lyrer, A J, Metso, T, Brandt, M, Kloss, C, Lichy, I, Hausser, E, Touzé, H S, Markus, S, Abboud, V, Caso, A, Bersano, A, Grau, A, Altintas, P, Amouyel, T, Tatlisumak, J, Dallongeville, C, Grond-Ginsbach, Juan Jose, Martin
المصدر: International Journal of Stroke. 4:224-230
بيانات النشر: SAGE Publications, 2009.
سنة النشر: 2009
مصطلحات موضوعية: Adult, Quality Control, Pathology, medicine.medical_specialty, Candidate gene, Genotype, Vertebral artery dissection, Genome-wide association study, CAD, Disease, Environment, Bioinformatics, Polymorphism, Single Nucleotide, White People, Brain Ischemia, Gene Frequency, Risk Factors, Genetic predisposition, Humans, Medicine, Young adult, Stroke, Vertebral Artery Dissection, Polymorphism, Genetic, business.industry, DNA, medicine.disease, Treatment Outcome, Neurology, Research Design, business, Genome-Wide Association Study
الوصف: 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.
تدمد: 1747-4949
1747-4930
DOI: 10.1111/j.1747-4949.2009.00281.x
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2c7f6f79bc4b63eb5ec4b2689d10075
https://doi.org/10.1111/j.1747-4949.2009.00281.x
Rights: CLOSED
رقم الانضمام: edsair.doi.dedup.....f2c7f6f79bc4b63eb5ec4b2689d10075
قاعدة البيانات: OpenAIRE
الوصف
تدمد:17474949
17474930
DOI:10.1111/j.1747-4949.2009.00281.x