Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia |
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Authors: | Splawski Igor Timothy Katherine W Tateyama Michihiro Clancy Colleen E Malhotra Alka Beggs Alan H Cappuccio Francesco P Sagnella Giuseppe A Kass Robert S Keating Mark T |
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Affiliation: | Department of Cardiology, Children's Hospital, Harvard Medical School and Howard Hughes Medical Institute, Boston, MA 02115, USA. igor@enders.tch.harvard.edu |
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Abstract: | Every year, approximately 450,000 individuals in the United States die suddenly of cardiac arrhythmia. We identified a variant of the cardiac sodium channel gene SCN5A that is associated with arrhythmia in African Americans (P = 0.000028) and linked with arrhythmia risk in an African-American family (P = 0.005). In transfected cells, the variant allele (Y1102) accelerated channel activation, increasing the likelihood of abnormal cardiac repolarization and arrhythmia. About 13.2% of African Americans carry the Y1102 allele. Because Y1102 has a subtle effect on risk, most carriers will never have an arrhythmia. However, Y1102 may be a useful molecular marker for the prediction of arrhythmia susceptibility in the context of additional acquired risk factors such as the use of certain medications. |
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