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Growth differentiation factor 15 and cardiovascular risk: individual patient meta-analysis.
Kato, Eri Toda; Morrow, David A; Guo, Jianping; Berg, David D; Blazing, Michael A; Bohula, Erin A; Bonaca, Marc P; Cannon, Christopher P; de Lemos, James A; Giugliano, Robert P; Jarolim, Petr; Kempf, Tibor; Kristin Newby, L; O'Donoghue, Michelle L; Pfeffer, Marc A; Rifai, Nader; Wiviott, Stephen D; Wollert, Kai C; Braunwald, Eugene; Sabatine, Marc S.
Afiliação
  • Kato ET; Department of Cardiovascular Medicine and Department of Clinical Laboratory, Kyoto University Hospital, 54 Shogoin-kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan.
  • Morrow DA; TIMI Study Group, 60 Fenwood Road, 7th floor, Boston, MA 02115, USA.
  • Guo J; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
  • Berg DD; TIMI Study Group, 60 Fenwood Road, 7th floor, Boston, MA 02115, USA.
  • Blazing MA; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
  • Bohula EA; TIMI Study Group, 60 Fenwood Road, 7th floor, Boston, MA 02115, USA.
  • Bonaca MP; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
  • Cannon CP; Duke Clinical Research Institute, Duke University, 300 W. Morris Street, Durham, NC 27701, USA.
  • de Lemos JA; TIMI Study Group, 60 Fenwood Road, 7th floor, Boston, MA 02115, USA.
  • Giugliano RP; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
  • Jarolim P; Cardiovascular Division, Department of Medicine, University of Colorado School of Medicine, 13001 East 17th PIace, Aurora, CO 80045, USA.
  • Kempf T; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
  • Kristin Newby L; Division of Cardiology, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd, Dallas, TX 75390-9003, USA.
  • O'Donoghue ML; TIMI Study Group, 60 Fenwood Road, 7th floor, Boston, MA 02115, USA.
  • Pfeffer MA; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
  • Rifai N; Department of Pathology, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
  • Wiviott SD; Division of Molecular and Translational Cardiology, Department of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg-Str, 1. D-30625 Hannover, Germany.
  • Wollert KC; Duke Clinical Research Institute, Duke University, 300 W. Morris Street, Durham, NC 27701, USA.
  • Braunwald E; TIMI Study Group, 60 Fenwood Road, 7th floor, Boston, MA 02115, USA.
  • Sabatine MS; Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital, 75 Francis Street, Boston, MA 02115, USA.
Eur Heart J ; 44(4): 293-300, 2023 01 21.
Article em En | MEDLINE | ID: mdl-36303404
ABSTRACT

AIMS:

Levels of growth differentiation factor 15 (GDF-15), a cytokine secreted in response to cellular stress and inflammation, have been associated with multiple types of cardiovascular (CV) events. However, its comparative prognostic performance across different presentations of atherosclerotic cardiovascular disease (ASCVD) remains unknown. METHODS AND

RESULTS:

An individual patient meta-analysis was performed using data pooled from eight trials including 53 486 patients. Baseline GDF-15 concentration was analyzed as a continuous variable and using established cutpoints (<1200 ng/L, 1200-1800 ng/L, > 1800 ng/L) to evaluate its prognostic performance for CV death/hospitalization for heart failure (HHF), major adverse cardiovascular events (MACE), and their components using Cox models adjusted for clinical variables and established CV biomarkers. Analyses were further stratified on ASCVD status acute coronary syndrome (ACS), stabilized after recent ACS, and stable ASCVD. Overall, higher GDF-15 concentration was significantly and independently associated with an increased rate of CV death/HHF and MACE (P < 0.001 for each). However, while GDF-15 showed a robust and consistent independent association with CV death and HHF across all presentations of ASCVD, its prognostic association with future myocardial infarction (MI) and stroke only remained significant in patients stabilized after recent ACS or with stable ASCVD [hazard ratio (HR) 1.24, 95% confidence interval (CI) 1.17-1.31 and HR 1.16, 95% CI 1.05-1.28 for MI and stroke, respectively] and not in ACS (HR 0.98, 95% CI 0.90-1.06 and HR 0.87, 95% CI 0.39-1.92, respectively).

CONCLUSION:

Growth differentiation factor 15 consistently adds prognostic information for CV death and HHF across the spectrum of ASCVD. GDF-15 also adds prognostic information for MI and stroke beyond clinical risk factors and cardiac biomarkers but not in the setting of ACS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Acidente Vascular Cerebral / Aterosclerose / Síndrome Coronariana Aguda / Insuficiência Cardíaca / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Acidente Vascular Cerebral / Aterosclerose / Síndrome Coronariana Aguda / Insuficiência Cardíaca / Infarto do Miocárdio Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans Idioma: En Revista: Eur Heart J Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Japão