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Intestinal Microbiota and Derived Metabolites in Myocardial Fibrosis and Postoperative Atrial Fibrillation.
Nenna, Antonio; Laudisio, Alice; Taffon, Chiara; Fogolari, Marta; Spadaccio, Cristiano; Ferrisi, Chiara; Loreni, Francesco; Giacinto, Omar; Mastroianni, Ciro; Barbato, Raffaele; Rose, David; Salsano, Antonio; Santini, Francesco; Angeletti, Silvia; Crescenzi, Anna; Antonelli Incalzi, Raffaele; Chello, Massimo; Lusini, Mario.
Afiliação
  • Nenna A; Cardiac Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.
  • Laudisio A; Internal Medicine, Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy.
  • Taffon C; Pathology, Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy.
  • Fogolari M; Clinical Laboratory, Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy.
  • Spadaccio C; Cardiac Surgery, University of Cincinnati Medical Center, Cincinnati, OH 45219, USA.
  • Ferrisi C; Cardiothoracic Surgery, Lancashire Cardiac Centre, Blackpool Teaching Hospital, Blackpool FY3 8NP, UK.
  • Loreni F; Cardiac Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.
  • Giacinto O; Cardiac Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.
  • Mastroianni C; Cardiac Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.
  • Barbato R; Cardiac Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.
  • Rose D; Cardiac Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.
  • Salsano A; Cardiothoracic Surgery, Lancashire Cardiac Centre, Blackpool Teaching Hospital, Blackpool FY3 8NP, UK.
  • Santini F; Cardiac Surgery, Ospedale Policlinico San Martino, University of Genoa, 16126 Genoa, Italy.
  • Angeletti S; Cardiac Surgery, Ospedale Policlinico San Martino, University of Genoa, 16126 Genoa, Italy.
  • Crescenzi A; Clinical Laboratory, Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy.
  • Antonelli Incalzi R; Pathology, Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy.
  • Chello M; Internal Medicine, Fondazione Policlinico Universitario Campus Bio-Medico, 00128 Rome, Italy.
  • Lusini M; Cardiac Surgery, Fondazione Policlinico Universitario Campus Bio-Medico, Via Alvaro del Portillo 200, 00128 Rome, Italy.
Int J Mol Sci ; 25(11)2024 May 30.
Article em En | MEDLINE | ID: mdl-38892223
ABSTRACT
The high incidence of atrial fibrillation (AFib) following cardiac surgery (postoperative atrial fibrillation, POAF) relies on specific surgical features. However, in the setting of POAF, the role of the microbiome in the modulation of cardiac fibrosis is still not clear. This study aimed to analyze the effect of the microbiome and its main metabolic product (trimethylamine-N-oxide, TMAO) in the fibrosis of myocardial tissue, to investigate its role in POAF. Patients undergoing elective cardiac surgery with cardiopulmonary bypass, central atrio-caval cannulation and no history of AFib, were included. A fragment of the right atrium was analyzed for qualitative and mRNA-quantitative evaluation. A preoperative blood sample was analyzed with enzyme-linked immunosorbent assay (ELISA). A total of 100 patients have been included, with POAF occurring in 38%. Histologically, a higher degree of fibrosis, angiogenesis and inflammation has been observed in POAF. Quantitative evaluation showed increased mRNA expression of collagen-1, collagen-3, fibronectin, and transforming growth factor beta (TGFb) in the POAF group. ELISA analysis showed higher levels of TMAO, lipopolysaccharide and TGFb in POAF, with similar levels of sP-selectin and zonulin. TMAO ≥ 61.8 ng/mL (odds ratio, OR 2.88 [1.35-6.16], p = 0.006), preoperative hemoglobin < 13.1 g/dL (OR 2.37 [1.07-5.24], p = 0.033) and impaired right ventricular function (OR 2.38 [1.17-4.83], p = 0.017) were independent predictors of POAF. Also, TMAO was significantly associated with POAF by means of increased fibrosis. Gut microbiome product TMAO is crucial for myocardial fibrosis, which is a key factor for POAF. Patients in preoperative sinus rhythm who will develop POAF have increased genetic expression of pro-fibrotic genes and enhanced fibrosis in histological staining. Elevated TMAO level (≥61.8 ng/mL) is an independent risk factor for POAF.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Fibrose / Microbioma Gastrointestinal / Miocárdio Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrilação Atrial / Fibrose / Microbioma Gastrointestinal / Miocárdio Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Int J Mol Sci Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Itália
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