Critical Diagnostics Announces Cardiac Biomarker ST2 Predicts Outcomes in Ambulatory Chronic Heart Failure Patients

Multicenter, Prospective Study in over 1,100 Patients is Largest Ever for Novel Cardiac Biomarker

SAN DIEGO--()--Critical Diagnostics, the exclusive developer of the Presage® ST2 Assay, announces the publication of the Penn Heart Failure Study (PHFS) in an advance e-publication of the January 19, 2010 edition of Circulation: Heart Failure.1 The results of this study demonstrated that ST2 levels not only predict outcomes for ambulatory outpatients with chronic heart failure, they more effectively risk-stratify such patients.

In the multi-center cohort of 1,141 heart failure patients, those with high levels of ST2 were significantly more likely to have a heart transplant or to die during the three-year follow-up period than those with low levels of ST2. By identifying those patients at highest risk, physicians can more appropriately tailor treatments to each patient and maximize utility of scarce and expensive health care resources.

Dr. Bonnie Ky and colleagues found that patients in the highest ST2 tertile had a higher risk of adverse outcomes compared to the lowest tertile, with an unadjusted hazard ratio (HR) of 3.2 (p < 0.0001) that remained significant after multivariable adjustment (adjusted HR 1.9; p = 0.002). With each doubling of ST2, there was a 40 - 50% increased risk of death or cardiac transplantation in fully adjusted models.

The patients, who had been recruited from three tertiary-care centers (University of Pennsylvania, Case Western University, and University of Wisconsin), were followed for a median of 2.8 years. There were 267 adverse events over the period (23% of patients), defined as the combined endpoint of death or cardiac transplantation. ST2 levels were measured at baseline from a blood sample taken at the enrollment of each patient into the study. The investigators conducted statistical analyses to predict outcomes by examining clinical presentation as well as the cardiac biomarkers ST2 and NT-proBNP. The clinical presentation data was also used to determine a risk score for each patient using the validated Seattle Heart Failure Model (SHFM), and to confirm the independent clinical utility of ST2 over and above that of the prognostic clinical parameters of the SHFM and NT-proBNP.

“The researchers also found that more than one in seven chronic heart failure patients can be more appropriately risk-stratified when using ST2 and NT-proBNP in addition to the Seattle Heart Failure Model,” said Pat Arensdorf, Chief Executive Officer of Critical Diagnostics. “By using the Presage ST2 Assay, clinicians may be able to target heart failure therapy more appropriately.”

PHFS has provided the largest study of ST2 ever performed in chronic, stable heart failure. The findings of this research support the utility of ST2 for identification of high risk patients who may benefit from more aggressive therapy.

About Heart Failure

According to the American Heart Association, there are 5.8 million Americans living with Heart Failure, and the care of these patients will cost $39.2 billion in 2010. Heart Failure means that the heart is not pumping blood as effectively as needed to the rest of the body. Because blood carries oxygen and materials that nourish the rest of the body, other organs do not receive the nutrients that they need as a result and the body will signal the heart to pump harder. When a patient is in heart failure, the added strain on the heart will cause the cardiac muscle to release increased amounts of a chemical called ST2.

About Critical Diagnostics and ST2

Critical Diagnostics (www.criticaldiagnostics.com) develops products to help physicians optimize patient care in cardiovascular diseases, such as heart failure. Our high sensitivity Presage® ST2 Assay measures the level of ST2 in blood, identifying patients at increased risk of morbidity and mortality. ST2 has been evaluated in peer-reviewed publications and across multiple clinical studies, now spanning more than 20,000 subjects.

ST2 signals the presence of adverse cardiac remodeling and fibrosis, which occurs in response to myocardial infarction (MI), ischemia, or worsening heart failure. Remodeling and fibrosis can also contribute to the development of future adverse events, such as secondary MI or sudden cardiac death, and to progression of heart failure.

The Presage ST2 Assay helps clinicians assess patient prognosis in order to better personalize their care. By selecting the most appropriate treatments and interventions for each patient, a physician can maximize the clinical benefit from increasingly limited healthcare resources.

The Presage ST2 Assay is not available for sale in the USA, pending FDA clearance. The Presage ST2 Assay has attained CE Mark.

Reference

1. Bonnie Ky, MD, MSCE; Benjamin French, PhD; Kristin McCloskey; J. Eduardo Rame, MD; Erin McIntosh, BA; Puja Shahi, BA; Daniel Dries, MD, MPH; W.H. Wilson Tang, MD; Alan H.B. Wu, PhD; James C. Fang, MD; Rebecca Boxer, MD; Nancy K. Sweitzer, MD; PhD; Wayne Levy, MD; Lee Goldberg MD, MPH; Mariell Jessup, MD; Thomas P. Cappola, MD, ScM. High-Sensitivity ST2 for Prediction of Adverse Outcomes in Chronic Heart Failure. Circulation Heart Failure Jan 2011 e-publication ahead of print (doi:10.1161/CIRCHEARTFAILURE.110.958223).

Contacts

Critical Diagnostics
Anne Rubin
Director, Marketing
877-700-1250
arubin@criticaldiagnostics.com

Release Summary

ST2 Predicts Outcomes in Chronic Heart Failure. Critical Diagnostics Presage ST2 Assay measures ST2 levels. Improves risk scoring compared to Seattle Heart Failure Model.

Contacts

Critical Diagnostics
Anne Rubin
Director, Marketing
877-700-1250
arubin@criticaldiagnostics.com