Two siblings with early repolarization syndrome: clinical and genetic characterization by whole-exome sequencing
Abstract: Aims
The early repolarization syndrome (ERS) can cause ventricular fibrillation (VF) and sudden death in young, otherwise healthy individuals. There are limited data suggesting that ERS might be heritable. The aim of this study was to characterize the clinical phenotype and to identify a causal variant in an affected family using an exome-sequencing approach.
Methods and results
Early repolarization syndrome was diagnosed according to the recently proposed Shanghai ERS Score. After sequencing of known ERS candidate genes, whole-exome sequencing (WES) was performed. The index patient (23 years, female) showed a dynamic inferolateral early repolarization (ER) pattern and electrical storm with intractable VF. Isoproterenol enabled successful termination of electrical storm with no recurrence on hydroquinidine therapy during 33 months of follow-up. The index patient’s brother (25 years) had a persistent inferior ER pattern with malignant features and a history of syncope. Both parents were asymptomatic and showed no ER pattern. While there was no pathogenic variant in candidate genes, WES detected a novel missense variant affecting a highly conserved residue (p. H2245R) in the ANK3 gene encoding Ankyrin-G in the two siblings and the father.
Conclusion
We identified two siblings with a malignant ERS phenotype sharing a novel ANK3 variant. A potentially pathogenic role of the novel ANK3 variant is suggested by the direct interaction of Ankyrin-G with the cardiac sodium channel, however, more patients with ANK3 variants and ERS would be required to establish ANK3 as novel ERS susceptibility gene. Our study provides additional evidence that ERS might be a heritable condition
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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Europace. - 23, 5 (2021) , 775–780, ISSN: 1532-2092
- Event
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Veröffentlichung
- (where)
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Freiburg
- (who)
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Universität
- (when)
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2021
- Creator
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Steinfurt, Johannes
Bezzina, Connie R.
Biermann, Jürgen
Staudacher, Dawid
Marschall, Christoph
Trolese, Luca
Faber, Thomas
Dürschmied, Daniel Frank
Zehender, Manfred Karl-Heinz
Bode, Christoph
Wilde, Arthur A. M.
Odening, Katja Elisabeth
Lodder, Elisabeth M.
- DOI
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10.1093/europace/euaa357
- URN
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urn:nbn:de:bsz:25-freidok-1750561
- Rights
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Kein Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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25.03.2025, 1:48 PM CET
Data provider
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Steinfurt, Johannes
- Bezzina, Connie R.
- Biermann, Jürgen
- Staudacher, Dawid
- Marschall, Christoph
- Trolese, Luca
- Faber, Thomas
- Dürschmied, Daniel Frank
- Zehender, Manfred Karl-Heinz
- Bode, Christoph
- Wilde, Arthur A. M.
- Odening, Katja Elisabeth
- Lodder, Elisabeth M.
- Universität
Time of origin
- 2021