Background: Atrial fibrillation (AF) and atrial flutter (AFL) are common cardiac conduction disorders affecting many people. Recent studies on sporadic cases of AF/AFL showed a significant association of the single nucleotide polymorphism rs2200733T with the disease, suggesting a genetic factor in the development of the disease. Objectives: To determine the association of rs2200733 with AF/AFL derived from an Italian population sample. Subjects: 78 patients with AF/AFL and 348 controls took part in the study. Design: Genetic case-control study. Results: The results indicate that there is a positive, significant association between the rs2200733 T allele and patients with AF/AFL of Italian origin (allelic p < 0.001 with OR = 2.17). Conclusion: These results derived from a sample of the Italian population agree with previously reported findings from an Icelandic study, which also found that the minor allele rs2200733 was associated with AF/AFL disease.

Association of rs2200733 at 4q25 with atrial flutter/fibrillation diseases in Italian population

G. Condorelli;
2008-01-01

Abstract

Background: Atrial fibrillation (AF) and atrial flutter (AFL) are common cardiac conduction disorders affecting many people. Recent studies on sporadic cases of AF/AFL showed a significant association of the single nucleotide polymorphism rs2200733T with the disease, suggesting a genetic factor in the development of the disease. Objectives: To determine the association of rs2200733 with AF/AFL derived from an Italian population sample. Subjects: 78 patients with AF/AFL and 348 controls took part in the study. Design: Genetic case-control study. Results: The results indicate that there is a positive, significant association between the rs2200733 T allele and patients with AF/AFL of Italian origin (allelic p < 0.001 with OR = 2.17). Conclusion: These results derived from a sample of the Italian population agree with previously reported findings from an Icelandic study, which also found that the minor allele rs2200733 was associated with AF/AFL disease.
2008
sudden cardiac death; familial aggregation; PITX2 isoforms; fibrillation; risk; flutter; mutation; gene; expression; arrhythmia
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11699/9574
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