Prediction of the early response to spironolactone in resistant hypertension by the combination of matrix metalloproteinase-9 activity and arterial stiffness parameters

Author:

Rodríguez-Sánchez Elena1ORCID,Navarro-García José Alberto1,Aceves-Ripoll Jennifer1,González-Lafuente Laura1,Baldan-Martin Montserrat2,de la Cuesta Fernando2,Alvarez-Llamas Gloria34,Barderas María G2,Segura Julián15,Ruilope Luis M1567,Ruiz-Hurtado Gema157ORCID

Affiliation:

1. Cardiorenal Translational Laboratory, Institute of Research i+12, Hospital Universitario, 12 de Octubre, Madrid, Spain

2. Department of Vascular Physiopathology, Hospital Nacional de Parapléjicos (HNP), SESCAM, Toledo, Spain

3. Departament of Immunology, IIS-Fundación Jimenez Diaz-UAM, Madrid, Spain

4. REDINREN, Madrid, Spain

5. Hypertension Unit, Hospital Universitario, 12 de Octubre, Madrid, Spain

6. European University of Madrid, Madrid, Spain

7. CIBER-CV, Hospital Universitario, 12 de Octubre, Madrid, Spain

Abstract

Abstract Aims The aim of this study was to determine whether arterial stiffness assessed with the biochemical parameter active matrix metalloproteinase (MMP)-9 and the clinical parameters pulse pressure (PP) and pulse wave velocity predicts the response to spironolactone in resistant hypertension (RH). Methods and results Ambulatory blood pressure (BP) and active MMP-9 (measured by zymography and ELISA) were measured at baseline, and patients were classified as having pseudo-RH or RH. Patients with RH received spironolactone and the response was determined after 8 weeks by ambulatory BP monitoring: those who achieved BP goals were considered controlled (CRH) and those who did not were considered uncontrolled (UCRH). Plasma active MMP-9 was significantly higher in patients with RH than with pseudo-RH, and correlated with 24 h systolic BP and PP. Receiver operating characteristic analysis indicated that active MMP-9 could predict the response to spironolactone, and its combination with 24 h PP and pulse wave velocity significantly improved this prediction. Moreover, plasma of patients with UCRH induced the MMP-9 expression pathway. Conclusion We propose active MMP-9 as a useful biomarker to identify patients with RH who will not respond to spironolactone. Combining MMP-9 activity with classical arterial stiffness parameters improves the prediction of the clinical response to spironolactone and might contribute to guide the most appropriate therapeutic decisions for patients with RH.

Funder

Instituto de Salud Carlos III

Fondo Europeo de Desarrollo Regional

Fondo Social Europeo

Fundación SENEFRO/Sociedad Española de Nefrología

Fundación Renal Íñigo Álvarez de Toledo

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Cardiology and Cardiovascular Medicine

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