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J Am Heart Assoc ; 6(5)2017 May 08.
Artigo em Inglês | MEDLINE | ID: mdl-28483776

RESUMO

BACKGROUND: Bioprosthetic heart valves (BHVs), fabricated from glutaraldehyde-pretreated bovine pericardium or porcine aortic valves, are widely used for the surgical or interventional treatment of heart valve disease. Reoperation becomes increasingly necessary over time because of BHV dysfunction. METHODS AND RESULTS: Forty-seven explanted BHV aortic valve replacements were retrieved at reoperation for clinically severe BHV dysfunction over the period 2010-2016. Clinical explant analyses of BHV leaflets for calcium (atomic absorption spectroscopy) and oxidized amino acids, per mass spectroscopy, were primary end points. Comorbidities for earlier BHV explant included diabetes mellitus and coronary artery bypass grafting. Mean calcium levels in BHV leaflets were significantly increased compared with unimplanted BHV (P<0.001); however, time to reoperation did not differ comparing calcified and noncalcified BHV. BHV dityrosine, an oxidized amino acid cross-link, was significantly increased in the explants (227.55±33.27 µmol/mol [dityrosine/tyrosine]) but was undetectable in unimplanted leaflets (P<0.001). BHV regional analyses revealed that dityrosine, ranging from 57.5 to 227.8 µmol/mol (dityrosine/tyrosine), was detectable only in the midleaflet samples, indicating the site-specific nature of dityrosine formation. 3-Chlorotyrosine, an oxidized amino acid formed by myeloperoxidase-catalyzed chlorinating oxidants, correlated with BHV calcium content in leaflet explant analyses from coronary artery bypass graft patients (r=0.62, P=0.01) but was not significantly correlated with calcification in non-coronary artery bypass graft explanted BHV. CONCLUSIONS: Both increased BHV leaflet calcium levels and elevated oxidized amino acids were associated with bioprosthesis dysfunction necessitating reoperation; however, BHV calcium levels were not a determinant of implant duration, indicating a potentially important role for oxidized amino acid formation in BHV dysfunction.


Assuntos
Insuficiência da Valva Aórtica/etiologia , Estenose da Valva Aórtica/etiologia , Valva Aórtica/patologia , Bioprótese , Calcinose/etiologia , Cálcio/metabolismo , Implante de Prótese de Valva Cardíaca/instrumentação , Próteses Valvulares Cardíacas , Valvas Cardíacas/cirurgia , Estresse Oxidativo , Falha de Prótese , Adulto , Idoso , Idoso de 80 Anos ou mais , Valva Aórtica/metabolismo , Valva Aórtica/cirurgia , Insuficiência da Valva Aórtica/metabolismo , Insuficiência da Valva Aórtica/patologia , Insuficiência da Valva Aórtica/cirurgia , Estenose da Valva Aórtica/metabolismo , Estenose da Valva Aórtica/patologia , Estenose da Valva Aórtica/cirurgia , Calcinose/metabolismo , Calcinose/patologia , Calcinose/cirurgia , Comorbidade , Depsipeptídeos/metabolismo , Remoção de Dispositivo , Progressão da Doença , Feminino , Implante de Prótese de Valva Cardíaca/efeitos adversos , Valvas Cardíacas/metabolismo , Valvas Cardíacas/patologia , Humanos , Masculino , Espectrometria de Massas , Pessoa de Meia-Idade , Desenho de Prótese , Sistema de Registros , Fatores de Risco , Espectrofotometria Atômica , Fatores de Tempo , Resultado do Tratamento , Tirosina/análogos & derivados , Tirosina/metabolismo , Adulto Jovem
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