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Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score

BACKGROUND: Dysautonomia plays an ancillary role in the pathogenesis of Chronic Chagas Cardiomyopathy (CCC), but is the key factor causing digestive organic involvement. We investigated the ability of heart rate variability (HRV) for death risk stratification in CCC and compared alterations of HRV i...

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Autores principales: Silva, Luiz Eduardo Virgilio, Moreira, Henrique Turin, de Oliveira, Marina Madureira, Cintra, Lorena Sayore Suzumura, Salgado, Helio Cesar, Fazan, Rubens, Tinós, Renato, Rassi, Anis, Schmidt, André, Marin-Neto, J. Antônio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241264/
https://www.ncbi.nlm.nih.gov/pubmed/35765063
http://dx.doi.org/10.1186/s12938-022-01014-6
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author Silva, Luiz Eduardo Virgilio
Moreira, Henrique Turin
de Oliveira, Marina Madureira
Cintra, Lorena Sayore Suzumura
Salgado, Helio Cesar
Fazan, Rubens
Tinós, Renato
Rassi, Anis
Schmidt, André
Marin-Neto, J. Antônio
author_facet Silva, Luiz Eduardo Virgilio
Moreira, Henrique Turin
de Oliveira, Marina Madureira
Cintra, Lorena Sayore Suzumura
Salgado, Helio Cesar
Fazan, Rubens
Tinós, Renato
Rassi, Anis
Schmidt, André
Marin-Neto, J. Antônio
author_sort Silva, Luiz Eduardo Virgilio
collection PubMed
description BACKGROUND: Dysautonomia plays an ancillary role in the pathogenesis of Chronic Chagas Cardiomyopathy (CCC), but is the key factor causing digestive organic involvement. We investigated the ability of heart rate variability (HRV) for death risk stratification in CCC and compared alterations of HRV in patients with isolated CCC and in those with the mixed form (CCC + digestive involvement). Thirty-one patients with CCC were classified into three risk groups (low, intermediate and high) according to their Rassi score. A single-lead ECG was recorded for a period of 10–20 min, RR series were generated and 31 HRV indices were calculated. The HRV was compared among the three risk groups and regarding the associated digestive involvement. Four machine learning models were created to predict the risk class of patients. RESULTS: Phase entropy is decreased and the percentage of inflection points is increased in patients from the high-, compared to the low-risk group. Fourteen patients had the mixed form, showing decreased triangular interpolation of the RR histogram and absolute power at the low-frequency band. The best predictive risk model was obtained by the support vector machine algorithm (overall F1-score of 0.61). CONCLUSIONS: The mixed form of Chagas' disease showed a decrease in the slow HRV components. The worst prognosis in CCC is associated with increased heart rate fragmentation. The combination of HRV indices enhanced the accuracy of risk stratification. In patients with the mixed form of Chagas disease, a higher degree of sympathetic autonomic denervation may be associated with parasympathetic impairment.
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spelling pubmed-92412642022-06-30 Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score Silva, Luiz Eduardo Virgilio Moreira, Henrique Turin de Oliveira, Marina Madureira Cintra, Lorena Sayore Suzumura Salgado, Helio Cesar Fazan, Rubens Tinós, Renato Rassi, Anis Schmidt, André Marin-Neto, J. Antônio Biomed Eng Online Research BACKGROUND: Dysautonomia plays an ancillary role in the pathogenesis of Chronic Chagas Cardiomyopathy (CCC), but is the key factor causing digestive organic involvement. We investigated the ability of heart rate variability (HRV) for death risk stratification in CCC and compared alterations of HRV in patients with isolated CCC and in those with the mixed form (CCC + digestive involvement). Thirty-one patients with CCC were classified into three risk groups (low, intermediate and high) according to their Rassi score. A single-lead ECG was recorded for a period of 10–20 min, RR series were generated and 31 HRV indices were calculated. The HRV was compared among the three risk groups and regarding the associated digestive involvement. Four machine learning models were created to predict the risk class of patients. RESULTS: Phase entropy is decreased and the percentage of inflection points is increased in patients from the high-, compared to the low-risk group. Fourteen patients had the mixed form, showing decreased triangular interpolation of the RR histogram and absolute power at the low-frequency band. The best predictive risk model was obtained by the support vector machine algorithm (overall F1-score of 0.61). CONCLUSIONS: The mixed form of Chagas' disease showed a decrease in the slow HRV components. The worst prognosis in CCC is associated with increased heart rate fragmentation. The combination of HRV indices enhanced the accuracy of risk stratification. In patients with the mixed form of Chagas disease, a higher degree of sympathetic autonomic denervation may be associated with parasympathetic impairment. BioMed Central 2022-06-28 /pmc/articles/PMC9241264/ /pubmed/35765063 http://dx.doi.org/10.1186/s12938-022-01014-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Silva, Luiz Eduardo Virgilio
Moreira, Henrique Turin
de Oliveira, Marina Madureira
Cintra, Lorena Sayore Suzumura
Salgado, Helio Cesar
Fazan, Rubens
Tinós, Renato
Rassi, Anis
Schmidt, André
Marin-Neto, J. Antônio
Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score
title Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score
title_full Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score
title_fullStr Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score
title_full_unstemmed Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score
title_short Heart rate variability as a biomarker in patients with Chronic Chagas Cardiomyopathy with or without concomitant digestive involvement and its relationship with the Rassi score
title_sort heart rate variability as a biomarker in patients with chronic chagas cardiomyopathy with or without concomitant digestive involvement and its relationship with the rassi score
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9241264/
https://www.ncbi.nlm.nih.gov/pubmed/35765063
http://dx.doi.org/10.1186/s12938-022-01014-6
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