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Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population

BACKGROUND: Intraventricular conduction delays (IVCDs) are hallmarks of heart failure (HF) and structural heart disease (SHD) but their prognostic value for HF and SHD is unclear. METHODS: Relation of eight IVCDs and the incidence of first-time HF or SHD was studied in a nationally representative ra...

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Autores principales: Rankinen, Jani, Haataja, Petri, Lyytikäinen, Leo-Pekka, Huhtala, Heini, Lehtimäki, Terho, Kähönen, Mika, Eskola, Markku, Pérez-Riera, Andrés Ricardo, Jula, Antti, Niiranen, Teemu, Nikus, Kjell, Hernesniemi, Jussi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522339/
https://www.ncbi.nlm.nih.gov/pubmed/33015317
http://dx.doi.org/10.1016/j.ijcha.2020.100639
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author Rankinen, Jani
Haataja, Petri
Lyytikäinen, Leo-Pekka
Huhtala, Heini
Lehtimäki, Terho
Kähönen, Mika
Eskola, Markku
Pérez-Riera, Andrés Ricardo
Jula, Antti
Niiranen, Teemu
Nikus, Kjell
Hernesniemi, Jussi
author_facet Rankinen, Jani
Haataja, Petri
Lyytikäinen, Leo-Pekka
Huhtala, Heini
Lehtimäki, Terho
Kähönen, Mika
Eskola, Markku
Pérez-Riera, Andrés Ricardo
Jula, Antti
Niiranen, Teemu
Nikus, Kjell
Hernesniemi, Jussi
author_sort Rankinen, Jani
collection PubMed
description BACKGROUND: Intraventricular conduction delays (IVCDs) are hallmarks of heart failure (HF) and structural heart disease (SHD) but their prognostic value for HF and SHD is unclear. METHODS: Relation of eight IVCDs and the incidence of first-time HF or SHD was studied in a nationally representative random sample of 6080 Finnish subjects aged ≥ 30 years (mean age 52.1, SD 14.5 years) who participated in the health examination including 12-lead ECG. RESULTS: During 16.5 years’ follow up, half of the subjects with left bundle branch block (LBBB) and one third of the subjects with non-specific IVCD developed HF. After controlling for known clinical risk factors the hazard ratio (HR) for new-onset HF for LBBB was 3.29 (95% confidence interval 1.93–5.63, P < 0.001) and 3.53 for non-specific IVCD (1.65–7.55, P = 0.001). In corresponding analysis, LBBB predicted SHD with HR 2.60 (1.21–5.62, P = 0.015). Excluding subjects with history of heart disease, including coronary heart disease, did not have impact on results. Right bundle branch block and other IVCDs displayed no relation to endpoints. CONCLUSION: LBBB and non-specific IVCD were associated with more than three-fold risk of new-onset HF. Furthermore, LBBB was associated with novel SHD. Their presence should alert clinician even in subjects free from any known heart disease.
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spelling pubmed-75223392020-10-02 Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population Rankinen, Jani Haataja, Petri Lyytikäinen, Leo-Pekka Huhtala, Heini Lehtimäki, Terho Kähönen, Mika Eskola, Markku Pérez-Riera, Andrés Ricardo Jula, Antti Niiranen, Teemu Nikus, Kjell Hernesniemi, Jussi Int J Cardiol Heart Vasc Original Paper BACKGROUND: Intraventricular conduction delays (IVCDs) are hallmarks of heart failure (HF) and structural heart disease (SHD) but their prognostic value for HF and SHD is unclear. METHODS: Relation of eight IVCDs and the incidence of first-time HF or SHD was studied in a nationally representative random sample of 6080 Finnish subjects aged ≥ 30 years (mean age 52.1, SD 14.5 years) who participated in the health examination including 12-lead ECG. RESULTS: During 16.5 years’ follow up, half of the subjects with left bundle branch block (LBBB) and one third of the subjects with non-specific IVCD developed HF. After controlling for known clinical risk factors the hazard ratio (HR) for new-onset HF for LBBB was 3.29 (95% confidence interval 1.93–5.63, P < 0.001) and 3.53 for non-specific IVCD (1.65–7.55, P = 0.001). In corresponding analysis, LBBB predicted SHD with HR 2.60 (1.21–5.62, P = 0.015). Excluding subjects with history of heart disease, including coronary heart disease, did not have impact on results. Right bundle branch block and other IVCDs displayed no relation to endpoints. CONCLUSION: LBBB and non-specific IVCD were associated with more than three-fold risk of new-onset HF. Furthermore, LBBB was associated with novel SHD. Their presence should alert clinician even in subjects free from any known heart disease. Elsevier 2020-09-25 /pmc/articles/PMC7522339/ /pubmed/33015317 http://dx.doi.org/10.1016/j.ijcha.2020.100639 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Paper
Rankinen, Jani
Haataja, Petri
Lyytikäinen, Leo-Pekka
Huhtala, Heini
Lehtimäki, Terho
Kähönen, Mika
Eskola, Markku
Pérez-Riera, Andrés Ricardo
Jula, Antti
Niiranen, Teemu
Nikus, Kjell
Hernesniemi, Jussi
Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population
title Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population
title_full Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population
title_fullStr Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population
title_full_unstemmed Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population
title_short Relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population
title_sort relation of intraventricular conduction delay to risk of new-onset heart failure and structural heart disease in the general population
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522339/
https://www.ncbi.nlm.nih.gov/pubmed/33015317
http://dx.doi.org/10.1016/j.ijcha.2020.100639
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