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Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea

Detalhes bibliográficos
Ano de defesa: 2020
Autor(a) principal: Renata da Cunha Ribeiro
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/1843/34719
Resumo: Introduction: According to the Brazilian Society of Cardiology, in Brazil there is 1 death from cardiovascular causes every 90 seconds and cardiovascular disease causes twice as many deaths as those due to all types of cancer combined. Although a decrease in ischemia-related mortality has been observed in recent years and its pathophysiology has been extensively studied, there are still unanswered questions, such as the role of the new components of the Renin-Angiotensin System (RAS). Objectives: To evaluate the profile of the RAS peptides, Alamandine, Angiotensin-(1-7), Angiotensin I and Angiotensin II, in cardiac patients undergoing isolated Cardiac Catheterism or followed by Percutaneous Angioplasty because Acute Coronary Syndrome and evaluate mRNA expression of ACE2, AT1 and Mas receptors in the same group of patients. Materials and Methods: 26 patients who underwent cardiac catheterism followed or not by Percutaneous Angioplasty were recruited. The Groups were divided according the use of medication or not, hypertension or not, the result of catheterism (normal or not) and Angioplasty. In each patient, blood was collected from the peripheral vein and the aortic root. In patients who underwent Angioplasty, blood was also collected at the same locations 5 minutes after Angioplasty. Alamandine, Angiotensin-(1-7), Angiotensin I and Angiotensin II were measured in each patient using Mass Spectrometry and research for AT1, Mas and ECA2 receptor mRNA in arterial blood polymorphonuclear cells (PBMC). Results: Alamandine and Angiotensin II increase with the degree of coronary disease. Angiotensin-(1-7) has its lowest absolute value in patients undergoing Angioplasty, while Angiotensin I presents, in patients undergoing Angioplasty, an intermediate value between those who have had a result of normal and injured Catetherism. After Angioplasty, Alamandine had a predominance of pulmonary formation, while Angiotensin I and Angiotensin II had a predominance of degradation. Angiotensin-(1-7) maintained a balance between these two phenomena after Angioplasty. The conversion of Angiotensin I to Angiotensin II as well as the Angiotensin- (1-7) / Angiotensin II ratio vary according to the degree of coronary disease, the medication used by the patient and the presence or not of Hypertension. The degree of coronary disease seems to have little influence on the expression of the studied receptors and also on the AT1 / Mas ratio. Discussion: We have few studies in humans that measure the values of the studied peptides. Most studies involving patients focus on clinical outcomes and stent restenosis. Our results were different from those found in the literature due to its design and method of measuring peptides. However, our data suggests that the degree of coronary disease as well as Angioplasty affect the plasma value of circulating Angiotensis and their pulmonary processing. These changes appear to be co-influenced by the use of medications such as Beta Blockers, ACEi and ARA and also by patient’s comorbidities. In contrast, the ACE2, AT1 and Mas receptors, as well as the AT1 / Mas ratio seems to be little influenced by the factors mentioned. Conclusion: Studies on patients are expensive and difficult from an ethical point of view due to the heterogeneity of the sample, thus leading to the need for a large number of patients and/or follow-up for a long period. Despite the limitations, our data suggest that the RAS is influenced by both the degree of coronary disease and the medications used by the patient, which also influence the patient’s response to Angioplasty. The ACE2, AT1 and Mas receptors are less sensitive to the factors mentioned.
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spelling 2021-01-15T14:43:17Z2025-09-09T00:00:59Z2021-01-15T14:43:17Z2020-07-08https://hdl.handle.net/1843/34719Introduction: According to the Brazilian Society of Cardiology, in Brazil there is 1 death from cardiovascular causes every 90 seconds and cardiovascular disease causes twice as many deaths as those due to all types of cancer combined. Although a decrease in ischemia-related mortality has been observed in recent years and its pathophysiology has been extensively studied, there are still unanswered questions, such as the role of the new components of the Renin-Angiotensin System (RAS). Objectives: To evaluate the profile of the RAS peptides, Alamandine, Angiotensin-(1-7), Angiotensin I and Angiotensin II, in cardiac patients undergoing isolated Cardiac Catheterism or followed by Percutaneous Angioplasty because Acute Coronary Syndrome and evaluate mRNA expression of ACE2, AT1 and Mas receptors in the same group of patients. Materials and Methods: 26 patients who underwent cardiac catheterism followed or not by Percutaneous Angioplasty were recruited. The Groups were divided according the use of medication or not, hypertension or not, the result of catheterism (normal or not) and Angioplasty. In each patient, blood was collected from the peripheral vein and the aortic root. In patients who underwent Angioplasty, blood was also collected at the same locations 5 minutes after Angioplasty. Alamandine, Angiotensin-(1-7), Angiotensin I and Angiotensin II were measured in each patient using Mass Spectrometry and research for AT1, Mas and ECA2 receptor mRNA in arterial blood polymorphonuclear cells (PBMC). Results: Alamandine and Angiotensin II increase with the degree of coronary disease. Angiotensin-(1-7) has its lowest absolute value in patients undergoing Angioplasty, while Angiotensin I presents, in patients undergoing Angioplasty, an intermediate value between those who have had a result of normal and injured Catetherism. After Angioplasty, Alamandine had a predominance of pulmonary formation, while Angiotensin I and Angiotensin II had a predominance of degradation. Angiotensin-(1-7) maintained a balance between these two phenomena after Angioplasty. The conversion of Angiotensin I to Angiotensin II as well as the Angiotensin- (1-7) / Angiotensin II ratio vary according to the degree of coronary disease, the medication used by the patient and the presence or not of Hypertension. The degree of coronary disease seems to have little influence on the expression of the studied receptors and also on the AT1 / Mas ratio. Discussion: We have few studies in humans that measure the values of the studied peptides. Most studies involving patients focus on clinical outcomes and stent restenosis. Our results were different from those found in the literature due to its design and method of measuring peptides. However, our data suggests that the degree of coronary disease as well as Angioplasty affect the plasma value of circulating Angiotensis and their pulmonary processing. These changes appear to be co-influenced by the use of medications such as Beta Blockers, ACEi and ARA and also by patient’s comorbidities. In contrast, the ACE2, AT1 and Mas receptors, as well as the AT1 / Mas ratio seems to be little influenced by the factors mentioned. Conclusion: Studies on patients are expensive and difficult from an ethical point of view due to the heterogeneity of the sample, thus leading to the need for a large number of patients and/or follow-up for a long period. Despite the limitations, our data suggest that the RAS is influenced by both the degree of coronary disease and the medications used by the patient, which also influence the patient’s response to Angioplasty. The ACE2, AT1 and Mas receptors are less sensitive to the factors mentioned.Outra AgênciaporUniversidade Federal de Minas GeraisAlamandinaAngiotensina-(1-7)Angiotensina IAngiotensina IIreceptor AT1receptor Masreceptor ACE2RNAmAngioplastiaCateterismo CardíacoSíndrome Coronariana AgudaInfarto Agudo do Miocárdio sem Supra STAngiotensinasAngiotensina IAngiotensina IIReceptor tipo 1 de angiotensinaRNA mensageiroAngioplastiaCateterismo cardíacoSíndrome coronariana agudaInfarto do miocárdio sem supradesnível do segmento STAvaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutâneainfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisRenata da Cunha Ribeiroinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMGhttp://lattes.cnpq.br/3591980542333447Robson Augusto Souza dos Santoshttp://lattes.cnpq.br/3919711591553904Bruno Ramos NascimentoAlmir de Sousa MartinsAnna Cristina Rodrigues SteinnFernando Antônio BotoniMaria Cláudia Costa IrigoyenIntrodução: Segundo a Sociedade Brasileira de Cardiologia, no Brasil ocorre uma morte de causa cardiovascular a cada 90 segundos e a doença cardiovascular causa o dobro da quantidade de mortes provenientes de todos os tipos de câncer juntos. Apesar de, nos últimos anos, terem sido observados diminuição da mortalidade relacionada à isquemia e da sua fisiopatologia ter sido exaustivamente estudada, ainda existem perguntas sem resposta, como o papel dos novos componentes do Sistema Renina-Angiotensina (SRA). Objetivos: Avaliar o perfil dos peptídeos do SRA, Alamandina, Angiotensina-(1-7), Angiotensina I e Angiotensina II, em pacientes cardiopatas submetidos ao cateterismo Cardíaco isolado ou seguido por Angioplastia Percutânea devido a Síndrome Coronariana Aguda e avaliar a expressão de RNAm dos receptores ACE2, AT1 e Mas no mesmo grupo de pacientes. Materiais e Métodos: 26 pacientes submetidos ao cateterismo Cardíaco seguido ou não por Angioplastia Percutânea foram recrutados. Os grupos foram divididos de acordo com o uso de medicamentos ou não, HAS ou não, o resultado do cateterismo (normal ou com lesão) e Angioplastia. Em cada paciente, foi colhido sangue na veia periférica no membro superior (direito ou esquerdo) e na raiz da aorta. Nos pacientes que realizaram Angioplastia, também foi colhido sangue nos mesmos locais 5 minutos após a Angioplastia. Nos pacientes foram feita dosagem arterial e venosa de Alamandina, Angiotensina-(1-7), Angiotensina I e Angiotensina II através de Espectrometria de Massa e pesquisa para RNAm dos receptores AT1, Mas e ECA2 em células polimorfonucleares de sangue arterial (PBMC). Resultados: A Alamadina e a Angiotensina II aumentam com o grau de coronariopatia. A Angiotensina-(1-7) apresenta seu menor valor absoluto em pacientes submetidos a Angioplastia, enquanto ao Angiotensina I apresenta, nos pacientes submetidos a Angioplastia, um valor intermediário entre aqueles que tiveram resultado de Cateterismo Normal e com Lesão. Após a Angioplastia, a Alamandina teve predomínio da formação pulmonar, enquanto a Angiotensina I e a Angiotensina II tiveram predomínio da degradação. A Angiotensina-(1-7) manteve um equilíbrio entre estes dois fenômenos após a Angioplastia. A conversão de Angiotensina I em Angiotensina II bem como a relação Angiotensina-(1-7)/Angiotensina II variam conforme o grau da coronariopatia, a medicação usada pelo paciente e a presença ou não de HAS. O grau de doença coronária parece ter pouca influência na expressão dos receptores estudados e também na relação AT1/Mas. Discussão: Temos poucos estudos em humanos que aferem os valores dos peptídeos estudados. A maioria dos estudos envolvendo pacientes foca em desfechos clínicos e re-estenose do stent. Nossos resultados foram diferentes daqueles encontrados na literatura devido ao desenho do mesmo e método de aferição dos peptídeos. Porém, nossos dados sugerem que o grau de doença coronária bem como a Angioplastia afetam o valor plasmático de Angiotensinas circulantes e o processamento pulmonar das mesmas. Essas alterações parecem ser co-influenciadas pelo uso de medicamentos como Beta Bloqueador, iECA e ARA e também pelas comorbidades dos pacientes. Em contra partida os receptores ACE2, AT1 e Mas, bem como a relação AT1/Mas parece ser pouco influenciada pelos fatores citados. Conclusão: Estudos em pacientes são caros e difíceis do ponto de vista ético devido à heterogeneidade da amostra, levando assim à necessidade de um número grande de pacientes e/ou acompanhamento por um longo período de tempo. Apesar das limitações, nossos resultados sugerem que o SRA sofre influência tanto do grau de coronariopatia, quanto das medicações usadas pelo paciente, que também influenciam a resposta do paciente à Angioplastia. Os receptores ACE2, AT1 e Mas são menos sensíveis aos fatores citados.BrasilICB - INSTITUTO DE CIÊNCIAS BIOLOGICASPrograma de Pós-Graduação em Ciências Biológicas - Fisiologia e FarmacologiaUFMGORIGINALdoutorado_rcr (1).pdfapplication/pdf5242487https://repositorio.ufmg.br//bitstreams/b77f5eec-82bf-471c-8154-069b4eebcad3/download8d0fa5e8785dda2070dc66a9a70ce648MD51trueAnonymousREADLICENSElicense.txttext/plain2119https://repositorio.ufmg.br//bitstreams/1170efa3-58d5-4aa5-a928-cb453d993286/download34badce4be7e31e3adb4575ae96af679MD52falseAnonymousREAD1843/347192025-09-08 21:00:59.973open.accessoai:repositorio.ufmg.br:1843/34719https://repositorio.ufmg.br/Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2025-09-09T00:00:59Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)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
dc.title.none.fl_str_mv Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
title Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
spellingShingle Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
Renata da Cunha Ribeiro
Angiotensinas
Angiotensina I
Angiotensina II
Receptor tipo 1 de angiotensina
RNA mensageiro
Angioplastia
Cateterismo cardíaco
Síndrome coronariana aguda
Infarto do miocárdio sem supradesnível do segmento ST
Alamandina
Angiotensina-(1-7)
Angiotensina I
Angiotensina II
receptor AT1
receptor Mas
receptor ACE2
RNAm
Angioplastia
Cateterismo Cardíaco
Síndrome Coronariana Aguda
Infarto Agudo do Miocárdio sem Supra ST
title_short Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
title_full Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
title_fullStr Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
title_full_unstemmed Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
title_sort Avaliação do perfil das angiotensinas em pacientes cardiopatas submetidos a angioplastia percutânea
author Renata da Cunha Ribeiro
author_facet Renata da Cunha Ribeiro
author_role author
dc.contributor.author.fl_str_mv Renata da Cunha Ribeiro
dc.subject.por.fl_str_mv Angiotensinas
Angiotensina I
Angiotensina II
Receptor tipo 1 de angiotensina
RNA mensageiro
Angioplastia
Cateterismo cardíaco
Síndrome coronariana aguda
Infarto do miocárdio sem supradesnível do segmento ST
topic Angiotensinas
Angiotensina I
Angiotensina II
Receptor tipo 1 de angiotensina
RNA mensageiro
Angioplastia
Cateterismo cardíaco
Síndrome coronariana aguda
Infarto do miocárdio sem supradesnível do segmento ST
Alamandina
Angiotensina-(1-7)
Angiotensina I
Angiotensina II
receptor AT1
receptor Mas
receptor ACE2
RNAm
Angioplastia
Cateterismo Cardíaco
Síndrome Coronariana Aguda
Infarto Agudo do Miocárdio sem Supra ST
dc.subject.other.none.fl_str_mv Alamandina
Angiotensina-(1-7)
Angiotensina I
Angiotensina II
receptor AT1
receptor Mas
receptor ACE2
RNAm
Angioplastia
Cateterismo Cardíaco
Síndrome Coronariana Aguda
Infarto Agudo do Miocárdio sem Supra ST
description Introduction: According to the Brazilian Society of Cardiology, in Brazil there is 1 death from cardiovascular causes every 90 seconds and cardiovascular disease causes twice as many deaths as those due to all types of cancer combined. Although a decrease in ischemia-related mortality has been observed in recent years and its pathophysiology has been extensively studied, there are still unanswered questions, such as the role of the new components of the Renin-Angiotensin System (RAS). Objectives: To evaluate the profile of the RAS peptides, Alamandine, Angiotensin-(1-7), Angiotensin I and Angiotensin II, in cardiac patients undergoing isolated Cardiac Catheterism or followed by Percutaneous Angioplasty because Acute Coronary Syndrome and evaluate mRNA expression of ACE2, AT1 and Mas receptors in the same group of patients. Materials and Methods: 26 patients who underwent cardiac catheterism followed or not by Percutaneous Angioplasty were recruited. The Groups were divided according the use of medication or not, hypertension or not, the result of catheterism (normal or not) and Angioplasty. In each patient, blood was collected from the peripheral vein and the aortic root. In patients who underwent Angioplasty, blood was also collected at the same locations 5 minutes after Angioplasty. Alamandine, Angiotensin-(1-7), Angiotensin I and Angiotensin II were measured in each patient using Mass Spectrometry and research for AT1, Mas and ECA2 receptor mRNA in arterial blood polymorphonuclear cells (PBMC). Results: Alamandine and Angiotensin II increase with the degree of coronary disease. Angiotensin-(1-7) has its lowest absolute value in patients undergoing Angioplasty, while Angiotensin I presents, in patients undergoing Angioplasty, an intermediate value between those who have had a result of normal and injured Catetherism. After Angioplasty, Alamandine had a predominance of pulmonary formation, while Angiotensin I and Angiotensin II had a predominance of degradation. Angiotensin-(1-7) maintained a balance between these two phenomena after Angioplasty. The conversion of Angiotensin I to Angiotensin II as well as the Angiotensin- (1-7) / Angiotensin II ratio vary according to the degree of coronary disease, the medication used by the patient and the presence or not of Hypertension. The degree of coronary disease seems to have little influence on the expression of the studied receptors and also on the AT1 / Mas ratio. Discussion: We have few studies in humans that measure the values of the studied peptides. Most studies involving patients focus on clinical outcomes and stent restenosis. Our results were different from those found in the literature due to its design and method of measuring peptides. However, our data suggests that the degree of coronary disease as well as Angioplasty affect the plasma value of circulating Angiotensis and their pulmonary processing. These changes appear to be co-influenced by the use of medications such as Beta Blockers, ACEi and ARA and also by patient’s comorbidities. In contrast, the ACE2, AT1 and Mas receptors, as well as the AT1 / Mas ratio seems to be little influenced by the factors mentioned. Conclusion: Studies on patients are expensive and difficult from an ethical point of view due to the heterogeneity of the sample, thus leading to the need for a large number of patients and/or follow-up for a long period. Despite the limitations, our data suggest that the RAS is influenced by both the degree of coronary disease and the medications used by the patient, which also influence the patient’s response to Angioplasty. The ACE2, AT1 and Mas receptors are less sensitive to the factors mentioned.
publishDate 2020
dc.date.issued.fl_str_mv 2020-07-08
dc.date.accessioned.fl_str_mv 2021-01-15T14:43:17Z
2025-09-09T00:00:59Z
dc.date.available.fl_str_mv 2021-01-15T14:43:17Z
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dc.publisher.none.fl_str_mv Universidade Federal de Minas Gerais
publisher.none.fl_str_mv Universidade Federal de Minas Gerais
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