Increased plasma concentrations of soluble ST2 are predictive for 1-year mortality in patients with acute destabilized heart failure.

@article{Mueller2008IncreasedPC,
  title={Increased plasma concentrations of soluble ST2 are predictive for 1-year mortality in patients with acute destabilized heart failure.},
  author={Thomas Mueller and Benjamin Dieplinger and Alfons Gegenhuber and Werner Poelz and R. Pacher and Meinhard Haltmayer},
  journal={Clinical chemistry},
  year={2008},
  volume={54 4},
  pages={
          752-6
        }
}
BACKGROUND The soluble isoform of the interleukin-1 receptor family member ST2 (sST2) has been implicated in heart failure. The aim of the present study was to evaluate the capability of sST2 as a prognostic marker in patients with acute destabilized heart failure. METHODS sST2 plasma concentrations were obtained in 137 patients with acute destabilized heart failure attending the emergency department of a tertiary care hospital. The endpoint was defined as all-cause mortality, and the study… 
Increased soluble ST2 predicts long-term mortality in patients with stable coronary artery disease: results from the Ludwigshafen risk and cardiovascular health study.
TLDR
Increased sST2 was an independent predictor of long-term all-cause mortality and provided complementary prognostic information to hs-cTnT and NT-proBNP and it was demonstrated that patients with all 3 biomarkers in the highest quartiles had the poorest outcome.
The Prognostic Value of Plasma Soluble ST2 in Hospitalized Chinese Patients with Heart Failure
Background sST2 has been shown to be a risk predictor in heart failure (HF). Our aim was to explore the characteristics and prognostic value of soluble ST2 (sST2) in hospitalized Chinese patients
High-Sensitivity ST2 for Prediction of Adverse Outcomes in Chronic Heart Failure
TLDR
ST2 is a potent marker of risk in chronic heart failure and when used in combination with NT-proBNP offers moderate improvement in assessing prognosis beyond clinical risk scores.
Serial Monitoring of Soluble Interleukin Family Member ST2 in Patients with Acutely Decompensated Heart Failure
TLDR
Among ADHF patients, sST2 concentrations tend to decrease following initiation of treatment and are prognostic both at presentation and during hospitalization, and may provide a basis for enhanced clinical decision making.
Soluble ST2 plasma concentrations predict 1-year mortality in acutely dyspneic emergency department patients with pulmonary disease.
TLDR
ST2 concentrations are frequently elevated in acute pulmonary diseases and are markedly prognostic for death by 1 year, and Cox proportional hazards models identified independent predictors of 1-year death.
Increased Soluble Suppression of Tumorigenicity 2 Level Predicts All-Cause and Cardiovascular Mortality in Maintenance Hemodialysis Patients: A Prospective Cohort Study
TLDR
The prognostic value of sST2 was additive to N-terminal pro-B-type natriuretic peptide (NT-proBNP) and high-sensitivity cardiac troponin T (hs-cTnT), as the combined use of s ST2 and NT- ProBNP or hs-c TnT better identified higher-risk patients.
Increased Soluble ST 2 Predicts Long-term Mortality in Patients with Stable Coronary Artery Disease : Results from the Ludwigshafen Risk and Cardiovascular Health Study
TLDR
It was demonstrated that patients with all 3 biomarkers in the highest quartiles had the poorest outcome, and the prognostic impact of sST2 was additive to NT-proBNP and hs-cTnT.
Prognostic value of sST2 added to BNP in acute heart failure with preserved or reduced ejection fraction
TLDR
sST2 provides robust prognostic information in acute heart failure with HFrEF, while this pattern was less clear in HFpEF, and when sST2 was measured together with BNP, it improved prognostic accuracy in both groups, more clearly in HFr EF.
Soluble ST2 as a Diagnostic and Prognostic Marker for Acute Heart Failure Syndromes.
TLDR
While sST2 was associated with AHFS readmission at 30-days, in the adjusted analyses it was not associated with adverse events, and s ST2 did not add significant information with regard to explaining the diagnostic and prognostic variability of BNP.
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  • DOI: 10.1373/clinchem.2007.096560 Brief Communications 756 Clinical Chemistry 54:4
  • 2008
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