Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas

Detalhes bibliográficos
Ano de defesa: 2024
Autor(a) principal: Sandra Monetti Dumont Sanches
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Minas Gerais
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://hdl.handle.net/1843/76595
Resumo: Chagas disease (Chd) is a neglected tropical disease that has a variable clinical course and can manifest in indeterminate (IF), cardiac, digestive, or cardio-digestive forms. The most prevalent determined form is chronic chagasic cardiomyopathy (CCC), characterized by by progressive ventricular dysfunction, complex arrhythmia and sudden death, linked to autonomic dysfunction, among other mechanisms. Esophageal dysfunction may be an indirect marker of enteric autonomic impairment observed in the digestive form. We aimed to evaluate the possible association between esophageal and cardiac autonomic denervation in indeterminate and CCC forms. Sixty-one patients with a serological diagnosis of Chd were grouped into IF (28) and CCC (33), 54,1% women, mean age 57 years, submitted to esophageal scintigraphy and esophageal transit time (ETT) and percentage of esophageal emptying (%EE) were recorded. Patients also underwent 24-hour Holter monitoring and heart rate variability (HRV) indices and ventricular extrasystole (VES) burden were reviewed by a cardiologist. The correlation between TTE, %EE, and HRV (SDNN - standard deviation of mean normal RR intervals, HFP - high-frequency power, LFP - low-frequency power), in addition to ESV in 24 hours were analyzed with IBM SPSS 23 software. The left ventricular ejection fraction was lower in the CCC group (44,0 ± 10,8 vs. 65,6 ± 5,7, p<0,001). Autonomic dysfunction showed a distinct pattern between IF and CCC, with lower SDNN andLF/HF values in the CCC group (100,0 ± 49,9 vs. 124,4 ± 43,9, p=0,049 e 1,4 (0,9 - 2,2) vs. 4,7 (1, 7 - 9,6), p<0,001, respectively). The CCM group also had higher 24h VES values 890,0 (120,0 - 2743,0) vs. 44,5 (1,2 3 228,7), p<0,001. There was significant inverse correlation between ETT and (ß=- 0,474, p<0,001), LFP (ms²) (ß=- 0,272, p=0,036), HFP (ms²) (ß=-0,363, p=0,004) and LH/FH (ß=-0,321, p=0,012) in the total sample. There was also a statistically significant and direct correlation between ETT and VES (ß=0,573, p=0,001) in the total sample. In conclusion, Chd patients with greater esophageal dysmotility showed a decrease in the oscillatory components of HRV and greater arrhythmic density, possibly as a result of more severe sympathetic and parasympathetic cardiac denervation.
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spelling Associação entre disfunção autonômica esofágica e cardíaca na doença de ChagasAssociation between esophageal and cardiac autonomic dysfunction in Chagas diseaseDoença de ChagasDenervação AutônomaTranstornos da Motilidade EsofágicaCintilografiaFrequência Cardíacadoença de Chagasdenervação autônomatranstornos da motilidade esofágicaCintilografiavariabilidade da frequência cardíacaChagas disease (Chd) is a neglected tropical disease that has a variable clinical course and can manifest in indeterminate (IF), cardiac, digestive, or cardio-digestive forms. The most prevalent determined form is chronic chagasic cardiomyopathy (CCC), characterized by by progressive ventricular dysfunction, complex arrhythmia and sudden death, linked to autonomic dysfunction, among other mechanisms. Esophageal dysfunction may be an indirect marker of enteric autonomic impairment observed in the digestive form. We aimed to evaluate the possible association between esophageal and cardiac autonomic denervation in indeterminate and CCC forms. Sixty-one patients with a serological diagnosis of Chd were grouped into IF (28) and CCC (33), 54,1% women, mean age 57 years, submitted to esophageal scintigraphy and esophageal transit time (ETT) and percentage of esophageal emptying (%EE) were recorded. Patients also underwent 24-hour Holter monitoring and heart rate variability (HRV) indices and ventricular extrasystole (VES) burden were reviewed by a cardiologist. The correlation between TTE, %EE, and HRV (SDNN - standard deviation of mean normal RR intervals, HFP - high-frequency power, LFP - low-frequency power), in addition to ESV in 24 hours were analyzed with IBM SPSS 23 software. The left ventricular ejection fraction was lower in the CCC group (44,0 ± 10,8 vs. 65,6 ± 5,7, p<0,001). Autonomic dysfunction showed a distinct pattern between IF and CCC, with lower SDNN andLF/HF values in the CCC group (100,0 ± 49,9 vs. 124,4 ± 43,9, p=0,049 e 1,4 (0,9 - 2,2) vs. 4,7 (1, 7 - 9,6), p<0,001, respectively). The CCM group also had higher 24h VES values 890,0 (120,0 - 2743,0) vs. 44,5 (1,2 3 228,7), p<0,001. There was significant inverse correlation between ETT and (ß=- 0,474, p<0,001), LFP (ms²) (ß=- 0,272, p=0,036), HFP (ms²) (ß=-0,363, p=0,004) and LH/FH (ß=-0,321, p=0,012) in the total sample. There was also a statistically significant and direct correlation between ETT and VES (ß=0,573, p=0,001) in the total sample. In conclusion, Chd patients with greater esophageal dysmotility showed a decrease in the oscillatory components of HRV and greater arrhythmic density, possibly as a result of more severe sympathetic and parasympathetic cardiac denervation.Universidade Federal de Minas Gerais2024-09-18T11:50:32Z2025-09-09T00:40:10Z2024-09-18T11:50:32Z2024-06-13info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfhttps://hdl.handle.net/1843/76595porSandra Monetti Dumont Sanchesinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2025-09-09T00:40:10Zoai:repositorio.ufmg.br:1843/76595Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2025-09-09T00:40:10Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false
dc.title.none.fl_str_mv Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
Association between esophageal and cardiac autonomic dysfunction in Chagas disease
title Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
spellingShingle Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
Sandra Monetti Dumont Sanches
Doença de Chagas
Denervação Autônoma
Transtornos da Motilidade Esofágica
Cintilografia
Frequência Cardíaca
doença de Chagas
denervação autônoma
transtornos da motilidade esofágica
Cintilografia
variabilidade da frequência cardíaca
title_short Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
title_full Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
title_fullStr Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
title_full_unstemmed Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
title_sort Associação entre disfunção autonômica esofágica e cardíaca na doença de Chagas
author Sandra Monetti Dumont Sanches
author_facet Sandra Monetti Dumont Sanches
author_role author
dc.contributor.author.fl_str_mv Sandra Monetti Dumont Sanches
dc.subject.por.fl_str_mv Doença de Chagas
Denervação Autônoma
Transtornos da Motilidade Esofágica
Cintilografia
Frequência Cardíaca
doença de Chagas
denervação autônoma
transtornos da motilidade esofágica
Cintilografia
variabilidade da frequência cardíaca
topic Doença de Chagas
Denervação Autônoma
Transtornos da Motilidade Esofágica
Cintilografia
Frequência Cardíaca
doença de Chagas
denervação autônoma
transtornos da motilidade esofágica
Cintilografia
variabilidade da frequência cardíaca
description Chagas disease (Chd) is a neglected tropical disease that has a variable clinical course and can manifest in indeterminate (IF), cardiac, digestive, or cardio-digestive forms. The most prevalent determined form is chronic chagasic cardiomyopathy (CCC), characterized by by progressive ventricular dysfunction, complex arrhythmia and sudden death, linked to autonomic dysfunction, among other mechanisms. Esophageal dysfunction may be an indirect marker of enteric autonomic impairment observed in the digestive form. We aimed to evaluate the possible association between esophageal and cardiac autonomic denervation in indeterminate and CCC forms. Sixty-one patients with a serological diagnosis of Chd were grouped into IF (28) and CCC (33), 54,1% women, mean age 57 years, submitted to esophageal scintigraphy and esophageal transit time (ETT) and percentage of esophageal emptying (%EE) were recorded. Patients also underwent 24-hour Holter monitoring and heart rate variability (HRV) indices and ventricular extrasystole (VES) burden were reviewed by a cardiologist. The correlation between TTE, %EE, and HRV (SDNN - standard deviation of mean normal RR intervals, HFP - high-frequency power, LFP - low-frequency power), in addition to ESV in 24 hours were analyzed with IBM SPSS 23 software. The left ventricular ejection fraction was lower in the CCC group (44,0 ± 10,8 vs. 65,6 ± 5,7, p<0,001). Autonomic dysfunction showed a distinct pattern between IF and CCC, with lower SDNN andLF/HF values in the CCC group (100,0 ± 49,9 vs. 124,4 ± 43,9, p=0,049 e 1,4 (0,9 - 2,2) vs. 4,7 (1, 7 - 9,6), p<0,001, respectively). The CCM group also had higher 24h VES values 890,0 (120,0 - 2743,0) vs. 44,5 (1,2 3 228,7), p<0,001. There was significant inverse correlation between ETT and (ß=- 0,474, p<0,001), LFP (ms²) (ß=- 0,272, p=0,036), HFP (ms²) (ß=-0,363, p=0,004) and LH/FH (ß=-0,321, p=0,012) in the total sample. There was also a statistically significant and direct correlation between ETT and VES (ß=0,573, p=0,001) in the total sample. In conclusion, Chd patients with greater esophageal dysmotility showed a decrease in the oscillatory components of HRV and greater arrhythmic density, possibly as a result of more severe sympathetic and parasympathetic cardiac denervation.
publishDate 2024
dc.date.none.fl_str_mv 2024-09-18T11:50:32Z
2024-09-18T11:50:32Z
2024-06-13
2025-09-09T00:40:10Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/1843/76595
url https://hdl.handle.net/1843/76595
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFMG
instname:Universidade Federal de Minas Gerais (UFMG)
instacron:UFMG
instname_str Universidade Federal de Minas Gerais (UFMG)
instacron_str UFMG
institution UFMG
reponame_str Repositório Institucional da UFMG
collection Repositório Institucional da UFMG
repository.name.fl_str_mv Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)
repository.mail.fl_str_mv repositorio@ufmg.br
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