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Comparison of longitudinal change in sST2 vs BNP to predict major adverse cardiovascular events in asymptomatic patients in the community.
Watson, Chris J; Tea, Isaac; O'Connell, Eoin; Glezeva, Nadezhda; Zhou, Shuaiwei; James, Stephanie; Gallagher, Joe; Snider, James; Januzzi, James L; Ledwidge, Mark T; McDonald, Ken M.
Afiliação
  • Watson CJ; Wellcome-Wolfson Institute for Experimental Medicine, Queen's University Belfast, Belfast, Northern Ireland.
  • Tea I; STOP-HF Group, St Vincent's University Hospital, Dublin, Ireland.
  • O'Connell E; UCD Conway Institute, School of Medicine, University College Dublin, Dublin, Ireland.
  • Glezeva N; Internal Medicine, Lankenau Medical Center, Wynnewood, PA, USA.
  • Zhou S; STOP-HF Group, St Vincent's University Hospital, Dublin, Ireland.
  • James S; UCD Conway Institute, School of Medicine, University College Dublin, Dublin, Ireland.
  • Gallagher J; STOP-HF Group, St Vincent's University Hospital, Dublin, Ireland.
  • Snider J; STOP-HF Group, St Vincent's University Hospital, Dublin, Ireland.
  • Januzzi JL; STOP-HF Group, St Vincent's University Hospital, Dublin, Ireland.
  • Ledwidge MT; UCD Conway Institute, School of Medicine, University College Dublin, Dublin, Ireland.
  • McDonald KM; Critical Diagnostics, San Diego, CA, USA.
J Cell Mol Med ; 24(11): 6495-6499, 2020 06.
Article em En | MEDLINE | ID: mdl-32347644
ABSTRACT
Biomarker-based preventative and monitoring strategies are increasingly used for risk stratification in cardiovascular (CV) disease. The aim of this study was to investigate the utility of longitudinal change in B-type natriuretic peptide (BNP) and sST2 concentrations for predicting incident major adverse CV events (MACE) (heart failure, myocardial infarction, arrhythmia, stroke/transient ischaemic attack and CV death) in asymptomatic community-based patients with risk factors but without prevalent MACE at enrolment. The study population consisted of 282 patients selected from the longitudinal STOP-HF study of asymptomatic patients with risk factors for development of MACE. Fifty-two of these patients developed a MACE. The study was run in two phases comprising of an initial investigative cohort (n = 195), and a subsequent 21 (No MACE MACE) propensity matched verification cohort (n = 87). BNP and sST2 were quantified in all patients at two time points a median of 2.5 years apart. Results highlighted that longitudinal change in sST2 was a statistically significant predictor of incident MACE, (AUC 0.60). A one-unit increment in sST2 change from baseline to follow up corresponded to approximately 7.99% increase in the rate of one or more incident MACE, independent of the baseline or follow-up concentration. In contrast, longitudinal change value of BNP was not associated with MACE. In conclusion, longitudinal change in sST2 but not BNP was associated with incident MACE in asymptomatic, initially event-free patients in the community. Further work is required to evaluate the clinical utility of change in sST2 in risk prediction and event monitoring in this setting.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores / Doenças Cardiovasculares / Sistema Cardiovascular / Peptídeo Natriurético Encefálico / Doenças Assintomáticas / Proteína 1 Semelhante a Receptor de Interleucina-1 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Biomarcadores / Doenças Cardiovasculares / Sistema Cardiovascular / Peptídeo Natriurético Encefálico / Doenças Assintomáticas / Proteína 1 Semelhante a Receptor de Interleucina-1 Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Cell Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2020 Tipo de documento: Article