Identify the Genes Polymorphisms Related to Non-familial Bradyarrhythmia

China Medical University

Status: Unknown

Conditions: Bradyarrhythmia

Study type: Observational

Funder types: Other

Identifiers

NCT01310907

DMR99-IRB-315

Details and patient eligibility

About

Bradyarrhythmia, including sinus node dysfunction and atrioventricular block, is a major cause necessitating pacemaker implantation. In contrast to familial bradyarrhythmia known as by mutations at particular ion channels, limited information is available for the mechanistic study in non-familial bradyarrhythmia.

Possible gene polymorphisms related to non-familial bradyarrhythmia were studied. Comparison of multi-locus analysis and single-locus analysis will be analyzed between the cases and controls. Functional studies will perform to clarify the results of association study.

Enrollment: 400 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• The patients with non-familial bradyarrhythmia

Exclusion criteria

• Familial bradyarrhythmia Reversible bradyarrhythmia Bradyarrhythmia after open heart surgery and severe organic heart diseases

Trial design

400 participants in 3 patient groups

sinus node dysfunction

Atrioventricular block

control