Prognostic value of circulating glypican-4 in chronic heart failure
Glypican-4 (GPC-4), an endothelial cell surface protein, is released into the circulation in the context of ischemia, inflammation, neurohumoral activity, and shear stress. This study aimed to investigate the prognostic value of GPC-4 in chronic heart failure. GPC-4 concentrations were determined in two prospective cohorts: patients with chronic heart failure with reduced ejection fraction (HFrEF), and with transthyretin amyloid cardiomyopathy (ATTR-CM). Multivariable Cox regression analyses were adjusted for age, sex, estimated glomerular filtration rate, N-terminal B-type natriuretic peptide, and left ventricular ejection fraction. In HFrEF (n = 205, median age 66 years, 22% women), 58 patients (28%) died, 18 (9%) from cardiovascular cause, and 46 patients (22%) were hospitalized for worsening heart failure (WHF) during 4.2 years follow-up. In ATTR-CM (n = 121, median age 76 years, 12% women), 34 patients (28%) died, 12 (10%) from cardiovascular cause, and 32 patients (26%) had a WHF hospitalization during 2.2 years follow-up. Baseline GPC-4 (median [interquartile range]) levels were 1553 (1041, 1950) pg/ml in HFrEF, and 2071 (1579, 2893) pg/mL in ATTR-CM. In HFrEF, GPC-4 was independently associated with all-cause mortality (HR 1.69, 95%CI 1.22-2.32, p = 0.003) and cardiovascular mortality (HR 1.61, 95%CI 1.01-2.56, p = 0.045), but not with WHF hospitalizations. Conclusively, in ATTR-CM, GPC-4 independently predicted all-cause mortality (HR 1.96, 95%CI 1.12-3.44, p = 0.018), but not cardiovascular mortality and WHF hospitalizations. GPC-4 carries strong prognostic value for all-cause death in chronic heart failure across various etiologies, but not for heart-failure specific outcomes. Further studies are warranted to elucidate its value in cardiovascular disease. KEY MESSAGES : Glypican-4 rises with ischemia, inflammation, neurohumoral activity, and shear stress. Circulating glypican-4 predicts prognosis in chronic heart failure, regardless of cause. Glypican-4 predicted all-cause death in heart failure with reduced ejection fraction and restrictive cardiomyopathy, but not heart failure-specific outcomes.
Authors
- Ewald Kolesnik (ORCID: https://orcid.org/0000-0002-9349-8068)
- Axel Muendlein (ORCID: https://orcid.org/0000-0002-5582-4125)
- ARTHUR MADER (ORCID: https://orcid.org/0000-0002-4897-2955)
- Klemens Ablasser
- Andreas Zirlik (ORCID: https://orcid.org/0000-0001-6290-3297)
- Viktoria Höller (ORCID: https://orcid.org/0009-0001-7024-2131)
- Andrea Borenich (ORCID: https://orcid.org/0000-0002-2966-253X)
- Martin Grübler (ORCID: https://orcid.org/0000-0002-1761-2914)
- Nicolas Verheyen (ORCID: https://orcid.org/0000-0001-7414-4056)
- Markus Wallner (ORCID: https://orcid.org/0000-0001-7692-892X)
- Andreas Leiherer (ORCID: https://orcid.org/0000-0003-3776-5704)
- Nora Schwegel (ORCID: https://orcid.org/0000-0001-8736-9625)
- Heinz Drexel (ORCID: https://orcid.org/0000-0002-4677-9756)
- Viktoria Santner (ORCID: https://orcid.org/0000-0001-8569-3683)
- Jakob Lugitsch
- Eva Maria Brandtner
- David Kajetan Zach
- Stefan Pilz
- Dirk von Lewinski
Institutions
- Sigmund Freud Privatuniversität Wien (AT)
- Danube Private University (AT)
- Medical University of Graz (AT)
- Fachhochschule Wiener Neustadt (AT)
- Vorarlberg Institute for Vascular Investigation and Treatment (AT)
Publication Details
- Journal
- Journal of Molecular Medicine
- Published
- 2026-04-07
- DOI
- https://doi.org/10.1007/s00109-026-02667-9
- Primary Topic
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Bristol-Myers Squibb
- Pfizer
- Karl-Franzens-Universität Graz
- Medizinische Universität Graz
- Swedish Orphan Biovitrum