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The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant
BACKGROUND: The arrhythmogenic cardiomyopathy (ACM) phenotype, with life-threatening ventricular arrhythmias and heart failure, varies according to genetic aetiology. We aimed to characterise the phenotype associated with the variant c.1211dup (p.Val406Serfs*4) in the plakophilin‑2 gene (PKP2) and c...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bohn Stafleu van Loghum
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400759/ https://www.ncbi.nlm.nih.gov/pubmed/37505369 http://dx.doi.org/10.1007/s12471-023-01791-2 |
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author | Bos, Thomas A. Piers, Sebastiaan R. D. Wessels, Marja W. Houweling, Arjan C. Bökenkamp, Regina Bootsma, Marianne Bosman, Laurens P. Evertz, Reinder Hellebrekers, Debby M. E. I. Hoedemaekers, Yvonne M. Knijnenburg, Jeroen Lekanne Deprez, Ronald van Mil, Anneke M. te Riele, Anneline S. J. M. van Slegtenhorst, Marjon A. Wilde, Arthur A. M. Yap, Sing-Chien Dooijes, Dennis Koopmann, Tamara T. van Tintelen, J. Peter Barge-Schaapveld, Daniela Q. C. M. |
author_facet | Bos, Thomas A. Piers, Sebastiaan R. D. Wessels, Marja W. Houweling, Arjan C. Bökenkamp, Regina Bootsma, Marianne Bosman, Laurens P. Evertz, Reinder Hellebrekers, Debby M. E. I. Hoedemaekers, Yvonne M. Knijnenburg, Jeroen Lekanne Deprez, Ronald van Mil, Anneke M. te Riele, Anneline S. J. M. van Slegtenhorst, Marjon A. Wilde, Arthur A. M. Yap, Sing-Chien Dooijes, Dennis Koopmann, Tamara T. van Tintelen, J. Peter Barge-Schaapveld, Daniela Q. C. M. |
author_sort | Bos, Thomas A. |
collection | PubMed |
description | BACKGROUND: The arrhythmogenic cardiomyopathy (ACM) phenotype, with life-threatening ventricular arrhythmias and heart failure, varies according to genetic aetiology. We aimed to characterise the phenotype associated with the variant c.1211dup (p.Val406Serfs*4) in the plakophilin‑2 gene (PKP2) and compare it with previously reported Dutch PKP2 founder variants. METHODS: Clinical data were collected retrospectively from medical records of 106 PKP2 c.1211dup heterozygous carriers. Using data from the Netherlands ACM Registry, c.1211dup was compared with 3 other truncating PKP2 variants (c.235C > T (p.Arg79*), c.397C > T (p.Gln133*) and c.2489+1G > A (p.?)). RESULTS: Of the 106 carriers, 47 (44%) were diagnosed with ACM, at a mean age of 41 years. By the end of follow-up, 29 (27%) had experienced sustained ventricular arrhythmias and 12 (11%) had developed heart failure, with male carriers showing significantly higher risks than females on these endpoints (p < 0.05). Based on available cardiac magnetic resonance imaging and echocardiographic data, 46% of the carriers showed either right ventricular dilatation and/or dysfunction, whereas a substantial minority (37%) had some form of left ventricular involvement. Both geographical distribution of carriers and haplotype analysis suggested PKP2 c.1211dup to be a founder variant originating from the South-Western coast of the Netherlands. Finally, a Cox proportional hazards model suggested significant differences in ventricular arrhythmia–free survival between 4 PKP2 founder variants, including c.1211dup. CONCLUSIONS: The PKP2 c.1211dup variant is a Dutch founder variant associated with a typical right-dominant ACM phenotype, but also left ventricular involvement, and a possibly more severe phenotype than other Dutch PKP2 founder variants. SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s12471-023-01791-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-10400759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Bohn Stafleu van Loghum |
record_format | MEDLINE/PubMed |
spelling | pubmed-104007592023-08-05 The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant Bos, Thomas A. Piers, Sebastiaan R. D. Wessels, Marja W. Houweling, Arjan C. Bökenkamp, Regina Bootsma, Marianne Bosman, Laurens P. Evertz, Reinder Hellebrekers, Debby M. E. I. Hoedemaekers, Yvonne M. Knijnenburg, Jeroen Lekanne Deprez, Ronald van Mil, Anneke M. te Riele, Anneline S. J. M. van Slegtenhorst, Marjon A. Wilde, Arthur A. M. Yap, Sing-Chien Dooijes, Dennis Koopmann, Tamara T. van Tintelen, J. Peter Barge-Schaapveld, Daniela Q. C. M. Neth Heart J Original Article BACKGROUND: The arrhythmogenic cardiomyopathy (ACM) phenotype, with life-threatening ventricular arrhythmias and heart failure, varies according to genetic aetiology. We aimed to characterise the phenotype associated with the variant c.1211dup (p.Val406Serfs*4) in the plakophilin‑2 gene (PKP2) and compare it with previously reported Dutch PKP2 founder variants. METHODS: Clinical data were collected retrospectively from medical records of 106 PKP2 c.1211dup heterozygous carriers. Using data from the Netherlands ACM Registry, c.1211dup was compared with 3 other truncating PKP2 variants (c.235C > T (p.Arg79*), c.397C > T (p.Gln133*) and c.2489+1G > A (p.?)). RESULTS: Of the 106 carriers, 47 (44%) were diagnosed with ACM, at a mean age of 41 years. By the end of follow-up, 29 (27%) had experienced sustained ventricular arrhythmias and 12 (11%) had developed heart failure, with male carriers showing significantly higher risks than females on these endpoints (p < 0.05). Based on available cardiac magnetic resonance imaging and echocardiographic data, 46% of the carriers showed either right ventricular dilatation and/or dysfunction, whereas a substantial minority (37%) had some form of left ventricular involvement. Both geographical distribution of carriers and haplotype analysis suggested PKP2 c.1211dup to be a founder variant originating from the South-Western coast of the Netherlands. Finally, a Cox proportional hazards model suggested significant differences in ventricular arrhythmia–free survival between 4 PKP2 founder variants, including c.1211dup. CONCLUSIONS: The PKP2 c.1211dup variant is a Dutch founder variant associated with a typical right-dominant ACM phenotype, but also left ventricular involvement, and a possibly more severe phenotype than other Dutch PKP2 founder variants. SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s12471-023-01791-2) contains supplementary material, which is available to authorized users. Bohn Stafleu van Loghum 2023-07-28 2023-08 /pmc/articles/PMC10400759/ /pubmed/37505369 http://dx.doi.org/10.1007/s12471-023-01791-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Bos, Thomas A. Piers, Sebastiaan R. D. Wessels, Marja W. Houweling, Arjan C. Bökenkamp, Regina Bootsma, Marianne Bosman, Laurens P. Evertz, Reinder Hellebrekers, Debby M. E. I. Hoedemaekers, Yvonne M. Knijnenburg, Jeroen Lekanne Deprez, Ronald van Mil, Anneke M. te Riele, Anneline S. J. M. van Slegtenhorst, Marjon A. Wilde, Arthur A. M. Yap, Sing-Chien Dooijes, Dennis Koopmann, Tamara T. van Tintelen, J. Peter Barge-Schaapveld, Daniela Q. C. M. The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant |
title | The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant |
title_full | The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant |
title_fullStr | The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant |
title_full_unstemmed | The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant |
title_short | The arrhythmogenic cardiomyopathy phenotype associated with PKP2 c.1211dup variant |
title_sort | arrhythmogenic cardiomyopathy phenotype associated with pkp2 c.1211dup variant |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400759/ https://www.ncbi.nlm.nih.gov/pubmed/37505369 http://dx.doi.org/10.1007/s12471-023-01791-2 |
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