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Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update

BACKGROUND: The genetic risk haplotype DPP6 has been linked to familial idiopathic ventricular fibrillation (IVF), but the associated long-term outcomes are unknown. METHODS: DPP6 risk haplotype-positive family members (DPP6 cases) and their risk haplotype-negative relatives (DPP6 controls) were inc...

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Autores principales: Bergeman, Auke T., Hoeksema, Wiert F., van der Ree, Martijn H., Boersma, Lucas V. A., Yap, Sing-Chien, Verheul, Lisa M., Hassink, Rutger J., van der Crabben, Saskia N., Volders, Paul G. A., van der Werf, Christian, Wilde, Arthur A. M., Postema, Pieter G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bohn Stafleu van Loghum 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400734/
https://www.ncbi.nlm.nih.gov/pubmed/37498467
http://dx.doi.org/10.1007/s12471-023-01792-1
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author Bergeman, Auke T.
Hoeksema, Wiert F.
van der Ree, Martijn H.
Boersma, Lucas V. A.
Yap, Sing-Chien
Verheul, Lisa M.
Hassink, Rutger J.
van der Crabben, Saskia N.
Volders, Paul G. A.
van der Werf, Christian
Wilde, Arthur A. M.
Postema, Pieter G.
author_facet Bergeman, Auke T.
Hoeksema, Wiert F.
van der Ree, Martijn H.
Boersma, Lucas V. A.
Yap, Sing-Chien
Verheul, Lisa M.
Hassink, Rutger J.
van der Crabben, Saskia N.
Volders, Paul G. A.
van der Werf, Christian
Wilde, Arthur A. M.
Postema, Pieter G.
author_sort Bergeman, Auke T.
collection PubMed
description BACKGROUND: The genetic risk haplotype DPP6 has been linked to familial idiopathic ventricular fibrillation (IVF), but the associated long-term outcomes are unknown. METHODS: DPP6 risk haplotype-positive family members (DPP6 cases) and their risk haplotype-negative relatives (DPP6 controls) were included. Clinical follow-up data were collected through March 2023. Implantable cardioverter-defibrillator (ICD) indication was divided in primary or secondary prevention. Cumulative survival and event rates were calculated. RESULTS: We included 327 DPP6 cases and 315 DPP6 controls. Median follow-up time was 9 years (interquartile range: 4–12). Of the DPP6 cases, 129 (39%) reached the composite endpoint of appropriate ICD shock, sudden cardiac arrest or death, at a median age of 45 years (range: 15–97). Median overall survival was 83 years and 87 years for DPP6 cases and DPP6 controls, respectively (p < 0.001). In DPP6 cases, median overall survival was shorter for males (74 years) than females (85 years) (p < 0.001). Of the DPP6 cases, 97 (30%) died, at a median age of 50 years. With a prophylactic ICD implantation advise based on risk haplotype, sex and age, 137 (42%) of DPP6 cases received an ICD, for primary prevention (n = 109) or secondary prevention (n = 28). In the primary prevention subgroup, 10 patients experienced a total of 34 appropriate ICD shocks, and there were no deaths during follow-up. DPP6 cases with a secondary prevention ICD experienced a total of 231 appropriate ICD shocks. CONCLUSION: Patients with the DPP6 risk haplotype, particularly males, are at an increased risk of IVF and sudden cardiac death. Using a risk stratification approach based on risk haplotype, sex and age, a substantial proportion of patients with a primary prevention ICD experienced appropriate ICD shocks, showing the benefit of prophylactic ICD implantation with this strategy.
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spelling pubmed-104007342023-08-05 Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update Bergeman, Auke T. Hoeksema, Wiert F. van der Ree, Martijn H. Boersma, Lucas V. A. Yap, Sing-Chien Verheul, Lisa M. Hassink, Rutger J. van der Crabben, Saskia N. Volders, Paul G. A. van der Werf, Christian Wilde, Arthur A. M. Postema, Pieter G. Neth Heart J Original Article BACKGROUND: The genetic risk haplotype DPP6 has been linked to familial idiopathic ventricular fibrillation (IVF), but the associated long-term outcomes are unknown. METHODS: DPP6 risk haplotype-positive family members (DPP6 cases) and their risk haplotype-negative relatives (DPP6 controls) were included. Clinical follow-up data were collected through March 2023. Implantable cardioverter-defibrillator (ICD) indication was divided in primary or secondary prevention. Cumulative survival and event rates were calculated. RESULTS: We included 327 DPP6 cases and 315 DPP6 controls. Median follow-up time was 9 years (interquartile range: 4–12). Of the DPP6 cases, 129 (39%) reached the composite endpoint of appropriate ICD shock, sudden cardiac arrest or death, at a median age of 45 years (range: 15–97). Median overall survival was 83 years and 87 years for DPP6 cases and DPP6 controls, respectively (p < 0.001). In DPP6 cases, median overall survival was shorter for males (74 years) than females (85 years) (p < 0.001). Of the DPP6 cases, 97 (30%) died, at a median age of 50 years. With a prophylactic ICD implantation advise based on risk haplotype, sex and age, 137 (42%) of DPP6 cases received an ICD, for primary prevention (n = 109) or secondary prevention (n = 28). In the primary prevention subgroup, 10 patients experienced a total of 34 appropriate ICD shocks, and there were no deaths during follow-up. DPP6 cases with a secondary prevention ICD experienced a total of 231 appropriate ICD shocks. CONCLUSION: Patients with the DPP6 risk haplotype, particularly males, are at an increased risk of IVF and sudden cardiac death. Using a risk stratification approach based on risk haplotype, sex and age, a substantial proportion of patients with a primary prevention ICD experienced appropriate ICD shocks, showing the benefit of prophylactic ICD implantation with this strategy. Bohn Stafleu van Loghum 2023-07-27 2023-08 /pmc/articles/PMC10400734/ /pubmed/37498467 http://dx.doi.org/10.1007/s12471-023-01792-1 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
Bergeman, Auke T.
Hoeksema, Wiert F.
van der Ree, Martijn H.
Boersma, Lucas V. A.
Yap, Sing-Chien
Verheul, Lisa M.
Hassink, Rutger J.
van der Crabben, Saskia N.
Volders, Paul G. A.
van der Werf, Christian
Wilde, Arthur A. M.
Postema, Pieter G.
Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
title Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
title_full Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
title_fullStr Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
title_full_unstemmed Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
title_short Outcomes in Dutch DPP6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
title_sort outcomes in dutch dpp6 risk haplotype for familial idiopathic ventricular fibrillation: a focused update
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400734/
https://www.ncbi.nlm.nih.gov/pubmed/37498467
http://dx.doi.org/10.1007/s12471-023-01792-1
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