Lipoprotein(a) and Calcific Aortic Valve Stenosis Progression

Author:

Arsenault Benoit J.12,Loganath Krithika3,Girard Arnaud1,Botezatu Simona34,Zheng Kang H.56,Tzolos Evangelos3,Abdoun Kathia1,Tastet Lionel1,Capoulade Romain7,Côté Nancy1,Craig Neil3,Chan Kwan L.8,Tam James W.9,Teo Koon K.10,Couture Christian1,Clavel Marie-Annick12,Mathieu Patrick111,Thériault Sébastien112,Stroes Erik S. G.5,Newby David E.3,Tsimikas Sotirios13,Pibarot Philippe12,Dweck Marc R.3

Affiliation:

1. Centre de recherche de l’Institut universitaire de cardiologie et de pneumologie de Québec, Université Laval, Québec, Canada

2. Department of Medicine, Faculty of Medicine, Université Laval, Québec, Québec, Canada

3. Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, United Kingdom

4. University of Medicine and Pharmacy Carol Davila, Cardiology Department, Euroecolab, Bucharest, Romania

5. Department of Vascular Medicine, Amsterdam University Medical Center, University of Amsterdam, Amsterdam, the Netherlands

6. Department of Cardiology, Onze Lieve Vrouwe Gasthuis Hospital, Amsterdam, the Netherlands

7. Nantes Université, Centre hospitalier universitaire Nantes, Centre national de recherche scientifique, Institut national de la santé et de la recherche médicale, l’institut du thorax, Nantes, France

8. Department of Medicine, University of Ottawa Heart Institute, Ottawa, Ontario, Canada

9. Department of Medicine, St Boniface General Hospital, Winnipeg, Manitoba, Canada

10. Department of Medicine (Cardiology), McMaster University, Hamilton, Ontario, Canada

11. Department of Surgery, Faculty of Medicine, Université Laval, Québec, Québec, Canada

12. Department of Molecular Biology, Medical Biochemistry and Pathology, Faculty of Medicine, Université Laval, Québec, Québec, Canada

13. Division of Cardiovascular Diseases, Department of Medicine, University of California, San Diego, La Jolla

Abstract

ImportanceThere are currently no pharmacological treatments available to slow hemodynamic progression of aortic stenosis. Plasma lipoprotein(a) concentrations predict incident aortic stenosis but its association with hemodynamic progression is controversial.ObjectiveTo determine the association between plasma lipoprotein(a) concentrations and hemodynamic progression in patients with aortic stenosis.Design, Settings and ParticipantsThe study included patients with aortic stenosis from 5 longitudinal clinical studies conducted from March 2001 to March 2023 in Canada and the UK. Of 757 total patients, data on plasma lipoprotein(a) concentrations and rates of hemodynamic progression assessed by echocardiography were available for 710, who were included in this analysis. Data were analyzed from March 2023 to April 2024.ExposureCohort-specific plasma lipoprotein(a) concentration tertiles.Main Outcomes and MeasuresHemodynamic aortic stenosis progression on echocardiography as assessed by annualized change in peak aortic jet velocity, mean transvalvular gradient, and aortic valve area.ResultsAmong the included patients, 497 (70%) were male and 213 (30%) were female. The mean (SD) age was 65.2 (13.1) years. Patients in the top lipoprotein(a) tertile demonstrated 41% (estimate, 1.41; 95% CI, 1.13-1.75) faster progression of peak aortic jet velocity and 57% (estimate, 1.57; 95% CI, 1.18-2.10) faster progression of mean transvalvular gradient than patients in the bottom tertile. There was no evidence of heterogeneity across the individual cohorts. Progression of aortic valve area was comparable between groups (estimate, 1.23; 95% CI, 0.71-2.12). Similar results were observed when plasma lipoprotein(a) concentrations were treated as a continuous variable.Conclusions and RelevanceIn this study, higher plasma lipoprotein(a) concentrations were associated with faster rates of hemodynamic progression in patients with aortic stenosis. Lowering plasma lipoprotein(a) concentrations warrants further investigation in the prevention and treatment of aortic stenosis.

Publisher

American Medical Association (AMA)

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