Orthostatic hypotension is associated with higher levels of circulating endostatin

Author:

Ricci Fabrizio123ORCID,Larsson Anders4ORCID,Ruge Toralph15ORCID,Galanti Kristian2,Hamrefors Viktor16ORCID,Sutton Richard7ORCID,Olshansky Brian8ORCID,Fedorowski Artur1910ORCID,Johansson Madeleine16ORCID

Affiliation:

1. Department of Clinical Sciences, Lund University , Malmö, Sweden, Jan Waldenströms gata 35, 214 28 Malmö , Sweden

2. Department of Neuroscience, Imaging and Clinical Sciences, ‘G.d'Annunzio’ University of Chieti-Pescara , Chieti , Italy

3. Heart Department, ‘SS Annunziata’ Polyclinic University Hospital , Chieti , Italy

4. Section of Clinical Chemistry, Department of Medical Sciences, Uppsala University , Uppsala , Sweden

5. Department of Emergency and Internal Medicine, Skåne University Hospital , Malmö , Sweden

6. Department of Cardiology, Skåne University Hospital , Malmö, Sweden, Jan Waldenströms gata 15, 214 28 Malmö , Sweden

7. Department of Cardiology, Hammersmith Hospital, National Heart and Lung Institute, Imperial College , London , UK

8. Division of Cardiology, Department of Internal Medicine, University of Iowa Hospitals and Clinics , Iowa City , USA

9. Department of Cardiology, Karolinska University Hospital , Stockholm , Sweden

10. Department of Medicine, Karolinska Institute , Stockholm , Sweden

Abstract

Abstract Aims The pathophysiology of orthostatic hypotension (OH), a common clinical condition, associated with adverse outcomes, is incompletely understood. We examined the relationship between OH and circulating endostatin, an endogenous angiogenesis inhibitor with antitumour effects proposed to be involved in blood pressure (BP) regulation. Methods and results We compared endostatin levels in 146 patients with OH and 150 controls. A commercial chemiluminescence sandwich immunoassay was used to measure circulating levels of endostatin. Linear and multivariate logistic regressions were conducted to test the association between endostatin and OH. Endostatin levels were significantly higher in OH patients (59 024 ± 2513 pg/mL) vs. controls (44 090 ± 1978pg/mL, P < 0.001). A positive linear correlation existed between endostatin and the magnitude of systolic BP decline upon standing (P < 0.001). Using multivariate analysis, endostatin was associated with OH (adjusted odds ratio per 10% increase of endostatin in the whole study population = 1.264, 95% confidence interval 1.141–1.402), regardless of age, sex, prevalent cancer, and cardiovascular disease, as well as traditional cardiovascular risk factors. Conclusion Circulating endostatin is elevated in patients with OH and may serve as a potential clinical marker of increased cardiovascular risk in patients with OH. Our findings call for external validation. Further research is warranted to clarify the underlying pathophysiological mechanisms.

Funder

ALF agreement

European Union—Next Generation EU

National Recovery and Resilience Plan

Italian Ministry of University

Swedish Heart Lung Foundation

Publisher

Oxford University Press (OUP)

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