Investigation of Genetic Risk of Atrial Fibrillation
Study Details
Study Description
Brief Summary
The atrial fibrillation (AF) is the most common cardiac rhythm disturbance that is responsible for substantial morbidity and mortality independent of associated heart disease or other risk factors. Even in the absence of preexisting cardiovascular disease, AF remains significantly associated with excess mortality rates. The current unsatisfactory treatment for AF comes from lack of understanding of the pathophysiology of AF. The purpose of this study is to identify gene polymorphisms that confer susceptibility to atrial fibrillation. Patients with AF(N=500) and healthy volunteer(N=1000) without AF are enrolled in this study. Patients with coronary artery disease, severe valvular heart disease, cardiomyopathy or heart failure were excluded from the study.
Condition or Disease | Intervention/Treatment | Phase |
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Study Design
Outcome Measures
Primary Outcome Measures
Eligibility Criteria
Criteria
Inclusion Criteria:
- Clinical diagnosis of atrial fibirillation
Exclusion Criteria:
-
coronary artery disease
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severe valvular heart disease
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cardiomyopathy
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heart failure
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
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1 | Department of Bio-information Analysis, Research Institute of Enviromental Medicine, Nagoya University | Nagoya | Aichi | Japan |
Sponsors and Collaborators
- Nagoya University
Investigators
- Study Chair: Kenji Yasui, MD, Phd, Department of Bio-information Analysis, Research Institute of Enviromental Medicine, Nagoya University
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- RIEM-G-1