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Published on: June 10, 2025
Prognostic impact of haemostatic derangements in chronic heart failure
Borut Jug1, Nina Vene, Barbara Guzic Salobir
1Department of Vascular Diseases, University Clinical Center Ljubljana, Zaloska 7/VI, Ljubljana, Slovenia. borut.jug@gmail.com
Insights
In chronic heart failure patients, elevated tissue plasminogen activator (tPA) antigen levels independently predict poor prognosis. Higher tPA levels indicate a greater risk of heart failure events, including death or hospitalization.
Area of Science:
- Cardiology
- Haemostasis Research
- Biomarker Discovery
Background:
- Heart failure is associated with an overactive blood clotting system (haemostasis).
- The prognostic significance of specific haemostatic markers in chronic heart failure remains incompletely understood.
Purpose of the Study:
- To investigate the prognostic value of key haemostatic markers in stable, outpatients with chronic heart failure.
- To determine if markers like prothrombin fragment F1+2, D-dimer, and tissue plasminogen activator (tPA) predict future adverse events.
Main Methods:
- 195 stable outpatients with chronic heart failure were enrolled.
- Baseline blood levels of prothrombin fragment F1+2, D-dimer, tPA, and PAI-1 antigens were measured.
- Patients were followed for adverse events (heart failure-related death or hospitalization).
Main Results:
- Patients experiencing an event had significantly higher levels of tPA antigen and D-dimer.
- Multivariate analysis identified elevated tPA antigen levels (above 10.2 microg/l) as an independent predictor of prognosis.
- D-dimer levels did not independently predict prognosis in this cohort.
Conclusions:
- Elevated tissue plasminogen activator (tPA) antigen levels are a significant and independent prognostic marker in patients with chronic stable heart failure.
- tPA may serve as a valuable biomarker for risk stratification in heart failure management.
Abstract:
Heart failure is characterised by activation of haemostasis. We sought to explore the prognostic impact of deranged haemostasis in chronic heart failure. In stable, optimally managed outpatients with chronic heart failure, baseline levels of prothrombin fragment F1+2, D-dimer, and tPA and PAI-1 antigens were determined. Clinical follow-up was obtained and the rate of events (heart failure related deaths or hospitalisations) was recorded. We included 195 patients [32.3% female, NYHA class II (66.2%) or III (33.8%), mean age 71 years]. During a median follow up of 693 (interquartile range [IQR] 574-788) days, 63 (30.9%) patients experienced an event; those with an event had higher levels of tPA antigen (median 11.8 [IQR 8.7-14.0] vs. 9.4 [7.9-12.1] microg/l; p = 0.033) and D-dimer (938 [485-1269] vs. 620 [37-1076] microg/l; p = 0.018). However, on Cox multivariate analysis, only tPA levels above optimal cut-off value of 10.2 microg/l (but not D-dimer) emerged as an independent predictor of prognosis (HR(adjusted) 2.695, 95% confidence interval 1.233-5.363; p = 0.017). Our findings suggest that elevated tPA antigen levels are an independent prognostic predictor in patients with chronic stable heart failure.
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