Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms

Naomasa Makita, Koji Sasaki, W. Antoinette Groenewegen, Takashi Yokota, Hisashi Yokoshiki, Tomoaki Murakami, Hiroyuki Tsutsui

Research output: Contribution to journalArticle

66 Citations (Scopus)

Abstract

Background: Congenital atrial standstill has been linked to SCN5A. Incomplete penetrance observed in atrial standstill has been attributed in part to the digenic inheritance of polymorphisms in the atrial-specific gap junction connexin 40 (Cx40) in conjunction with an SCN5A mutation. Objectives: The purpose of this study was to determine the clinical and biophysical characteristics of a novel SCN5A mutation identified in a family with atrial standstill. Methods: Family members of an apparently sporadic case of atrial standstill underwent genetic screening of SCN5A and atrial-specific genes including Cx40. Biophysical properties of the wild-type (WT) and mutant SCN5A channels in a heterologous expression system were studied using the whole-cell patch clamp technique. Results: The novel SCN5A mutation L212P was identified in the proband (age 11 years) and his father. The father was in normal sinus rhythm. The proband had no P waves on surface ECG, and his right atrium could not be captured by pacing. The recombinant L212P Na channel showed a large hyperpolarizing shift in both the voltage dependence of activation (WT: -48.1 ± 0.9 mV; L212P: -63.5 ± 1.5 mV; P < .001) and inactivation (WT: -86.6 ± 0.9 mV; L212P: -95.6 ± 0.8 mV; P < .001) and delayed recovery from inactivation. Further screenings for genetic variations that might mitigate L212P dysfunction revealed that the proband, but not his father, carries Cx40 polymorphisms inherited from his asymptomatic mother. Conclusion: These results suggest that genetic defects in SCN5A most likely underlie atrial standstill. Coinheritance of Cx40 polymorphisms is a possible genetic factor that modifies the clinical manifestation of this inherited arrhythmia.

Original languageEnglish
Pages (from-to)1128-1134
Number of pages7
JournalHeart Rhythm
Volume2
Issue number10
DOIs
Publication statusPublished - Oct 1 2005

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Mutation
Fathers
Penetrance
Gap Junctions
Genetic Testing
Patch-Clamp Techniques
Heart Atria
Cardiac Arrhythmias
Electrocardiography
Mothers
Atrial Standstill
connexin 40
Genes

All Science Journal Classification (ASJC) codes

  • Cardiology and Cardiovascular Medicine
  • Physiology (medical)

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Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms. / Makita, Naomasa; Sasaki, Koji; Groenewegen, W. Antoinette; Yokota, Takashi; Yokoshiki, Hisashi; Murakami, Tomoaki; Tsutsui, Hiroyuki.

In: Heart Rhythm, Vol. 2, No. 10, 01.10.2005, p. 1128-1134.

Research output: Contribution to journalArticle

Makita, Naomasa ; Sasaki, Koji ; Groenewegen, W. Antoinette ; Yokota, Takashi ; Yokoshiki, Hisashi ; Murakami, Tomoaki ; Tsutsui, Hiroyuki. / Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms. In: Heart Rhythm. 2005 ; Vol. 2, No. 10. pp. 1128-1134.
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AU - Makita, Naomasa

AU - Sasaki, Koji

AU - Groenewegen, W. Antoinette

AU - Yokota, Takashi

AU - Yokoshiki, Hisashi

AU - Murakami, Tomoaki

AU - Tsutsui, Hiroyuki

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AB - Background: Congenital atrial standstill has been linked to SCN5A. Incomplete penetrance observed in atrial standstill has been attributed in part to the digenic inheritance of polymorphisms in the atrial-specific gap junction connexin 40 (Cx40) in conjunction with an SCN5A mutation. Objectives: The purpose of this study was to determine the clinical and biophysical characteristics of a novel SCN5A mutation identified in a family with atrial standstill. Methods: Family members of an apparently sporadic case of atrial standstill underwent genetic screening of SCN5A and atrial-specific genes including Cx40. Biophysical properties of the wild-type (WT) and mutant SCN5A channels in a heterologous expression system were studied using the whole-cell patch clamp technique. Results: The novel SCN5A mutation L212P was identified in the proband (age 11 years) and his father. The father was in normal sinus rhythm. The proband had no P waves on surface ECG, and his right atrium could not be captured by pacing. The recombinant L212P Na channel showed a large hyperpolarizing shift in both the voltage dependence of activation (WT: -48.1 ± 0.9 mV; L212P: -63.5 ± 1.5 mV; P < .001) and inactivation (WT: -86.6 ± 0.9 mV; L212P: -95.6 ± 0.8 mV; P < .001) and delayed recovery from inactivation. Further screenings for genetic variations that might mitigate L212P dysfunction revealed that the proband, but not his father, carries Cx40 polymorphisms inherited from his asymptomatic mother. Conclusion: These results suggest that genetic defects in SCN5A most likely underlie atrial standstill. Coinheritance of Cx40 polymorphisms is a possible genetic factor that modifies the clinical manifestation of this inherited arrhythmia.

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