Proteomic profiles of left atrial volume and its influence on response to spironolactone: Findings from the HOMAGE trial and STANISLAS cohort

Author:

Kobayashi Masatake12,Ferreira João Pedro13,Duarte Kevin1,Bresso Emmanuel1,Huttin Olivier1,Bozec Erwan1,Brunner La Rocca Hans‐Peter4,Delles Christian5,Clark Andrew L.6,Edelmann Frank7,González Arantxa89,Heymans Stephane4,Pellicori Pierpaolo5,Petutschnigg Johannes10,Verdonschot Job A.J.4,Rossignol Patrick111,Cleland John G.F.5,Zannad Faiez1,Girerd Nicolas1,

Affiliation:

1. Université de Lorraine, INSERM, Centre d'Investigations Cliniques Plurithématique 1433, Inserm U1116, CHRU de Nancy and F‐CRIN INI‐CRCT Nancy France

2. Department of Cardiology Tokyo Medical University Hospital Tokyo Japan

3. Cardiovascular Research and Development Center, Department of Surgery and Physiology Faculty of Medicine of the University of Porto Porto Portugal

4. Department of Cardiology Maastricht University Medical Center Maastricht The Netherlands

5. School of Cardiovascular and Metabolic Health University of Glasgow Glasgow UK

6. Department of Cardiology University of Hull, Castle Hill Hospital Yorkshire UK

7. Department of Internal Medicine and Cardiology Campus Virchow Klinikum Charité University Medicine Berlin and German Centre for Cardiovascular Research (DZHK), Partner Site Berlin Berlin Germany

8. CIMA Universidad de Navarra, Department of Pathology Anatomy and Physiology Universidad de Navarra and IdiSNA Pamplona Spain

9. CIBERCV, Carlos III Institute of Health Madrid Spain

10. Department of Internal Medicine and/Cardiology Campus Virchow Klinikum, Charité University Medicine Berlin, and German Heart Center Berlin, and Berlin Institute of Health (BIH), and German Centre for Cardiovascular research (DZHK) Berlin Germany

11. Medical Specialties and Nephrology Dialysis Departments, Monaco Princess Grace Hospital and Monaco Private Hemodialysis Centre Monaco Monaco

Abstract

AimsHigh left ventricular filling pressure increases left atrial volume and causes myocardial fibrosis, which may decrease with spironolactone. We studied clinical and proteomic characteristics associated with left atrial volume indexed by body surface area (LAVi), and whether LAVi influences the response to spironolactone on biomarker expression and clinical variables.Methods and resultsIn the HOMAGE trial, where people at risk of heart failure were randomized to spironolactone or control, we analysed 421 participants with available LAVi and 276 proteomic measurements (Olink) at baseline, month 1 and 9 (mean age 73 ± 6 years; women 26%; LAVi 32 ± 9 ml/m2). Circulating proteins associated with LAVi were also assessed in asymptomatic individuals from a population‐based cohort (STANISLAS; n = 1640; mean age 49 ± 14 years; women 51%; LAVi 23 ± 7 ml/m2). In both studies, greater LAVi was significantly associated with greater left ventricular masses and volumes. In HOMAGE, after adjustment and correction for multiple testing, greater LAVi was associated with higher concentrations of matrix metallopeptidase‐2 (MMP‐2), insulin‐like growth factor binding protein‐2 (IGFBP‐2) and N‐terminal pro‐B‐type natriuretic peptide (NT‐proBNP) (false discovery rates [FDR] <0.05). These associations were externally replicated in STANISLAS (all FDR <0.05). Among these biomarkers, spironolactone decreased concentrations of MMP‐2 and NT‐proBNP, regardless of baseline LAVi (pinteraction > 0.10). Spironolactone also significantly reduced LAVi, improved left ventricular ejection fraction, lowered E/e', blood pressure and serum procollagen type I C‐terminal propeptide (PICP) concentration, a collagen synthesis marker, regardless of baseline LAVi (pinteraction > 0.10).ConclusionIn individuals without heart failure, LAVi was associated with MMP‐2, IGFBP‐2 and NT‐proBNP. Spironolactone reduced these biomarker concentrations as well as LAVi and PICP, irrespective of left atrial size.

Funder

Fonds Wetenschappelijk Onderzoek

Instituto de Salud Carlos III

Publisher

Wiley

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