Atrial natriuretic peptide frameshift mutation in familial atrial fibrillation

被引:263
作者
Hodgson-Zingman, Denice M. [2 ]
Karst, Margaret L. [1 ]
Zingman, Leonid V. [2 ]
Heublein, Denise M. [4 ,5 ]
Darbar, Dawood [1 ]
Herron, Kathleen J. [1 ]
Ballew, Jeffrey D. [1 ]
de Andrade, Mariza [6 ]
Burnett, John C., Jr. [4 ,5 ]
Olson, Timothy M. [1 ,3 ]
机构
[1] Mayo Clin, Coll Med, Dept Internal Med, Cardiovasc Genet Lab, Rochester, MN 55905 USA
[2] Univ Iowa, Carver Coll Med, Dept Internal Med, Iowa City, IA USA
[3] Mayo Clin, Coll Med, Dept Pediat & Adolescent Med, Rochester, MN 55905 USA
[4] Mayo Clin, Coll Med, Dept Physiol, Cardiorenal Res Lab, Rochester, MN 55905 USA
[5] Mayo Clin, Coll Med, Dept Internal Med, Cardiorenal Res Lab, Rochester, MN 55905 USA
[6] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN 55905 USA
关键词
D O I
10.1056/NEJMoa0706300
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Atrial fibrillation is a common arrhythmia that is hereditary in a small subgroup of patients. In a family with 11 clinically affected members, we mapped an atrial fibrillation locus to chromosome 1p36-p35 and identified a heterozygous frameshift mutation in the gene encoding atrial natriuretic peptide. Circulating chimeric atrial natriuretic peptide (ANP) was detected in high concentration in subjects with the mutation, and shortened atrial action potentials were seen in an isolated heart model, creating a possible substrate for atrial fibrillation. This report implicates perturbation of the atrial natriuretic peptide-cyclic guanosine monophosphate (cGMP) pathway in cardiac electrical instability. Copyright © 2008 Massachusetts Medical Society. All rights reserved.
引用
收藏
页码:158 / 165
页数:8
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