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Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy

FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private company. Main funding source(s): Pfizer Global Medical Grant BACKGROUND: Amyloid transthyretin cardiomyopathy (ATTR-CM) is a progressive infiltrative cardiomyopathy caused by extracellular deposition of amyloid fibrils. The disease is charac...

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Autores principales: Knoll, K, Fuchs, P, Weidmann, I, Gross, S, Altunkas, F, Lennerz, C, Kolb, C, Kessler, T, Schunkert, H, Hengstenberg, W, Trenkwalder, T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207568/
http://dx.doi.org/10.1093/europace/euad122.274
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author Knoll, K
Fuchs, P
Weidmann, I
Gross, S
Altunkas, F
Lennerz, C
Kolb, C
Kessler, T
Schunkert, H
Hengstenberg, W
Trenkwalder, T
author_facet Knoll, K
Fuchs, P
Weidmann, I
Gross, S
Altunkas, F
Lennerz, C
Kolb, C
Kessler, T
Schunkert, H
Hengstenberg, W
Trenkwalder, T
author_sort Knoll, K
collection PubMed
description FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private company. Main funding source(s): Pfizer Global Medical Grant BACKGROUND: Amyloid transthyretin cardiomyopathy (ATTR-CM) is a progressive infiltrative cardiomyopathy caused by extracellular deposition of amyloid fibrils. The disease is characterized by congestive heart failure, conduction abnormalities and arrhythmias. Due to the limited overall prognosis, ICDs were rarely indicated in ATTR-CM. However, with the development of new targeted therapies, the role of ICD therapy for ATTR-CM should be reevaluated. Hence, there is an urgent and unmet need to identify patients at high risk for ventricular tachycardias who might possibly benefit from ICD therapy. METHODS: Between 2020 and 2022, 120 patients were diagnosed with ATTR-CM in a tertiary referral center. Of those, 63 were prospectively evaluated for the presence of ventricular arrhythmias using 24 hours Holter-ECG. Ventricular arrhythmias were further characterized as sustained (sVT) and non-sustained ventricular tachycardias (nsVT). RESULTS: In our cohort of unselected ATTR-CMP patients the prevalence of ventricular tachycardias was high with 47.6 % (n= 30/63). Of those, the majority were non-sustained VTs (84%) and the minority sustained VT (16%). Patients with ventricular tachycardias showed significantly more severe left ventricular (LV) hypertrophy, reduced LV ejection fraction (LV-EF) and larger left atrial volumes as well as a trend towards smaller LV cavities (table 1). Interestingly, no significant differences in prevalence of coronary artery disease or cardiac markers such as NTproBNP and troponin were seen between patients with and without ventricular tachycardias (table 1). Furthermore, we evaluated the multivariable predictive performance for discriminating between patients with and without ventricular tachycardias using two backward variable selection procedures (model 1 p-value based and model 2 Akaike information criterion (AIC) based). In the first model, LVEF (OR = 0.865 [0.776;0.963], p=0.008), LVEED (0.837 [0.708;0.991], p=0.039), and LV mass indexed by BSA (1.028[1.003;1.055], p=0.031) remained independent predictors of occurrence of ventricular arrhythmias, while in the second model sodium concentration (1.287 [0.929;1.783], p=0.129) and betablocker medication (5.078, [0.819;31.477], p=0.081) also were retained. Comparing the area under the Receiver Operating-Characteristic (AUROC) we observed no significant difference between both models (AUROC: 0.846 [0.711;0.937] vs. 0.870 [0.737;0.951], p=0.57, figure 1). CONCLUSION: The prevalence of ventricular tachycardia in ATTR-CM is high. Patients with ventricular tachycardia show advanced stage of left ventricular disease, with LVEDD, LV-EF and LV mass indexed by BSA being predictors of ventricular tachycardias in two multivariable predictive models. Further studies validating the predictive value of those variables are needed, including the assessment of nsVT and sVT in predicting sudden cardiac death, possibly allowing the use as a risk score for ventricular arrhythmias. [Figure: see text] [Figure: see text]
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spelling pubmed-102075682023-05-25 Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy Knoll, K Fuchs, P Weidmann, I Gross, S Altunkas, F Lennerz, C Kolb, C Kessler, T Schunkert, H Hengstenberg, W Trenkwalder, T Europace 13.2 - Epidemiology, Prognosis, Outcome FUNDING ACKNOWLEDGEMENTS: Type of funding sources: Private company. Main funding source(s): Pfizer Global Medical Grant BACKGROUND: Amyloid transthyretin cardiomyopathy (ATTR-CM) is a progressive infiltrative cardiomyopathy caused by extracellular deposition of amyloid fibrils. The disease is characterized by congestive heart failure, conduction abnormalities and arrhythmias. Due to the limited overall prognosis, ICDs were rarely indicated in ATTR-CM. However, with the development of new targeted therapies, the role of ICD therapy for ATTR-CM should be reevaluated. Hence, there is an urgent and unmet need to identify patients at high risk for ventricular tachycardias who might possibly benefit from ICD therapy. METHODS: Between 2020 and 2022, 120 patients were diagnosed with ATTR-CM in a tertiary referral center. Of those, 63 were prospectively evaluated for the presence of ventricular arrhythmias using 24 hours Holter-ECG. Ventricular arrhythmias were further characterized as sustained (sVT) and non-sustained ventricular tachycardias (nsVT). RESULTS: In our cohort of unselected ATTR-CMP patients the prevalence of ventricular tachycardias was high with 47.6 % (n= 30/63). Of those, the majority were non-sustained VTs (84%) and the minority sustained VT (16%). Patients with ventricular tachycardias showed significantly more severe left ventricular (LV) hypertrophy, reduced LV ejection fraction (LV-EF) and larger left atrial volumes as well as a trend towards smaller LV cavities (table 1). Interestingly, no significant differences in prevalence of coronary artery disease or cardiac markers such as NTproBNP and troponin were seen between patients with and without ventricular tachycardias (table 1). Furthermore, we evaluated the multivariable predictive performance for discriminating between patients with and without ventricular tachycardias using two backward variable selection procedures (model 1 p-value based and model 2 Akaike information criterion (AIC) based). In the first model, LVEF (OR = 0.865 [0.776;0.963], p=0.008), LVEED (0.837 [0.708;0.991], p=0.039), and LV mass indexed by BSA (1.028[1.003;1.055], p=0.031) remained independent predictors of occurrence of ventricular arrhythmias, while in the second model sodium concentration (1.287 [0.929;1.783], p=0.129) and betablocker medication (5.078, [0.819;31.477], p=0.081) also were retained. Comparing the area under the Receiver Operating-Characteristic (AUROC) we observed no significant difference between both models (AUROC: 0.846 [0.711;0.937] vs. 0.870 [0.737;0.951], p=0.57, figure 1). CONCLUSION: The prevalence of ventricular tachycardia in ATTR-CM is high. Patients with ventricular tachycardia show advanced stage of left ventricular disease, with LVEDD, LV-EF and LV mass indexed by BSA being predictors of ventricular tachycardias in two multivariable predictive models. Further studies validating the predictive value of those variables are needed, including the assessment of nsVT and sVT in predicting sudden cardiac death, possibly allowing the use as a risk score for ventricular arrhythmias. [Figure: see text] [Figure: see text] Oxford University Press 2023-05-24 /pmc/articles/PMC10207568/ http://dx.doi.org/10.1093/europace/euad122.274 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the European Society of Cardiology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle 13.2 - Epidemiology, Prognosis, Outcome
Knoll, K
Fuchs, P
Weidmann, I
Gross, S
Altunkas, F
Lennerz, C
Kolb, C
Kessler, T
Schunkert, H
Hengstenberg, W
Trenkwalder, T
Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy
title Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy
title_full Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy
title_fullStr Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy
title_full_unstemmed Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy
title_short Left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy
title_sort left ventricular hypertrophy, dilatation and ejection fractions predict ventricular tachycardia in amyloid transthyretin cardiomyopathy
topic 13.2 - Epidemiology, Prognosis, Outcome
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10207568/
http://dx.doi.org/10.1093/europace/euad122.274
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