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Proteomic Signatures During Treatment in Different Stages of Heart Failure.
Michelhaugh, Sam A; Camacho, Alexander; Ibrahim, Nasrien E; Gaggin, Hanna; D'Alessandro, David; Coglianese, Erin; Lewis, Gregory D; Januzzi, James L.
Afiliação
  • Michelhaugh SA; Massachusetts General Hospital, Boston (S.A.M., A.C., N.E.I., H.G., D.D., E.C., G.D.L., J.L.J.).
  • Camacho A; Massachusetts General Hospital, Boston (S.A.M., A.C., N.E.I., H.G., D.D., E.C., G.D.L., J.L.J.).
  • Ibrahim NE; Massachusetts General Hospital, Boston (S.A.M., A.C., N.E.I., H.G., D.D., E.C., G.D.L., J.L.J.).
  • Gaggin H; Harvard Medical School, Boston, MA (N.E.I., H.G., E.G., G.D.L., J.L.J.).
  • D'Alessandro D; Massachusetts General Hospital, Boston (S.A.M., A.C., N.E.I., H.G., D.D., E.C., G.D.L., J.L.J.).
  • Coglianese E; Harvard Medical School, Boston, MA (N.E.I., H.G., E.G., G.D.L., J.L.J.).
  • Lewis GD; Massachusetts General Hospital, Boston (S.A.M., A.C., N.E.I., H.G., D.D., E.C., G.D.L., J.L.J.).
  • Januzzi JL; Massachusetts General Hospital, Boston (S.A.M., A.C., N.E.I., H.G., D.D., E.C., G.D.L., J.L.J.).
Circ Heart Fail ; 13(8): e006794, 2020 08.
Article em En | MEDLINE | ID: mdl-32809875
BACKGROUND: Proteomics have already provided novel insights into the pathophysiology of heart failure (HF) with reduced ejection fraction. Previous studies have evaluated cross-sectional protein signatures of HF, but few have characterized proteomic changes following HF with reduced ejection fraction treatment with ARNI (angiotensin receptor/neprilysin inhibitor) therapy or left ventricular assist devices. METHODS: In this retrospective omics study, we performed targeted proteomics (N=625) of whole blood sera from patients with American College of Cardiology/American Heart Association stage D (N=29) and stage C (N=12) HF using proximity extension assays. Samples were obtained before and after (median=82 days) left ventricular assist device implantation (stage D; primary analysis) and ARNI therapy initiation (stage C; matched reference). Oblique principal component analysis and point biserial correlations were used for feature extraction and selection; standardized mean differences were used to assess within and between-group differences; and enrichment analysis was used to generate and cluster Gene Ontology terms. RESULTS: Core sets of proteins were identified for stage C (N=9 proteins) and stage D (N=18) HF; additionally, a core set of 5 shared HF proteins (NT-proBNP [N-terminal pro-B type natriuretic peptide], ESM [endothelial cell-specific molecule]-1, cathepsin L1, osteopontin, and MCSF-1) was also identified. For patients with stage D HF, moderate (δ, 0.40-0.60) and moderate-to-large (δ, 0.60-0.80) sized differences were observed in 8 of their 18 core proteins after left ventricular assist devices implantation. Additionally, specific protein groups reached concentration levels equivalent (g<0.10) to stage C HF after initiation on ARNI therapy. CONCLUSIONS: HF with reduced ejection fraction severity associates with distinct proteomic signatures that reflect underlying disease attributes; these core signatures may be useful for monitoring changes in cardiac function following initiation on ARNI or left ventricular assist device implantation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteômica / Antagonistas de Receptores de Angiotensina / Insuficiência Cardíaca Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteômica / Antagonistas de Receptores de Angiotensina / Insuficiência Cardíaca Idioma: En Ano de publicação: 2020 Tipo de documento: Article