Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1785084510095802368 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10400734 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Bohn Stafleu van Loghum |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT bergemanauket outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT hoeksemawiertf outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT vanderreemartijnh outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT boersmalucasva outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT yapsingchien outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT verheullisam outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT hassinkrutgerj outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT vandercrabbensaskian outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT volderspaulga outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT vanderwerfchristian outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT wildearthuram outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT postemapieterg outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate AT outcomesindutchdpp6riskhaplotypeforfamilialidiopathicventricularfibrillationafocusedupdate |