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Fibrinogen and the prediction of residual obstruction manifested after pulmonary embolism treatment.
Planquette, Benjamin; Sanchez, Olivier; Marsh, James J; Chiles, Peter G; Emmerich, Joseph; Le Gal, Grégoire; Meyer, Guy; Wolfson, Tanya; Gamst, Anthony C; Moore, Roger E; Gugiu, Gabriel B; Morris, Timothy A.
Afiliação
  • Planquette B; Université Paris Descartes, Sorbonne Paris Cité, France.
  • Sanchez O; Service de Pneumologie et Soins Intensifs, Hôpital Européen Georges Pompidou, AP-HP, Paris, France.
  • Marsh JJ; INSERM UMR-S 1140, Paris, France.
  • Chiles PG; Université Paris Descartes, Sorbonne Paris Cité, France.
  • Emmerich J; Service de Pneumologie et Soins Intensifs, Hôpital Européen Georges Pompidou, AP-HP, Paris, France.
  • Le Gal G; INSERM UMR-S 1140, Paris, France.
  • Meyer G; Dept of Medicine, Division of Pulmonary and Critical Care Medicine, University of California, San Diego, CA, USA.
  • Wolfson T; Dept of Medicine, Division of Pulmonary and Critical Care Medicine, University of California, San Diego, CA, USA.
  • Gamst AC; Université Paris Descartes, Sorbonne Paris Cité, France.
  • Moore RE; Médecine Vasculaire - Cardiologie, Centre de Diagnostic et de Thérapeutique, Hôpital Hôtel Dieu, AP-HP, Paris, France.
  • Gugiu GB; Dept of Medicine, Ottawa Hospital Research Institute, University of Ottawa, Ottawa, ON, Canada.
  • Morris TA; Université Paris Descartes, Sorbonne Paris Cité, France.
Eur Respir J ; 52(5)2018 11.
Article em En | MEDLINE | ID: mdl-30337447
ABSTRACT
Residual pulmonary vascular obstruction (RPVO) and chronic thromboembolic pulmonary hypertension (CTEPH) are both long-term complications of acute pulmonary embolism, but it is unknown whether RPVO can be predicted by variants of fibrinogen associated with CTEPH.We used the Akaike information criterion to select the best predictive models for RPVO in two prospectively followed cohorts of acute pulmonary embolism patients, using as candidate variables the extent of the initial obstruction, clinical characteristics and fibrinogen-related data. We measured the selected models' goodness of fit by analysis of deviance and compared models using the Chi-squared test.RPVO occurred in 29 (28.4%) out of 102 subjects in the first cohort and 46 (25.3%) out of 182 subjects in the second. The best-fit predictive model derived in the first cohort (p=0.0002) and validated in the second cohort (p=0.0005) implicated fibrinogen Bß-chain monosialylation in the development of RPVO. When the derivation procedure excluded clinical characteristics, fibrinogen Bß-chain monosialylation remained a predictor of RPVO in the best-fit predictive model (p=0.00003). Excluding fibrinogen characteristics worsened the predictive model (p=0.03).Fibrinogen Bß-chain monosialylation, a common structural attribute of fibrin, helped predict RPVO after acute pulmonary embolism. Fibrin structure may contribute to the risk of developing RPVO.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arteriopatias Oclusivas / Artéria Pulmonar / Embolia Pulmonar / Fibrinogênio Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Arteriopatias Oclusivas / Artéria Pulmonar / Embolia Pulmonar / Fibrinogênio Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged País como assunto: Europa Idioma: En Ano de publicação: 2018 Tipo de documento: Article