Left Ventricular Hypertrophy and Biomarkers of Cardiac Damage and Stress in Aortic Stenosis

Author:

Stein Elliot J.1ORCID,Fearon William F.2ORCID,Elmariah Sammy3ORCID,Kim Juyong B.2ORCID,Kapadia Samir4ORCID,Kumbhani Dharam J.5ORCID,Gillam Linda6ORCID,Whisenant Brian7ORCID,Quader Nishath8,Zajarias Alan8,Welt Frederick G.9ORCID,Bavry Anthony A.5ORCID,Coylewright Megan10ORCID,Piana Robert N.11,Mallugari Ravinder R.11,Clark Daniel E.11ORCID,Patel Jay N.11,Gonzales Holly11,Gupta Deepak K.11ORCID,Vatterott Anna8,Jackson Natalie1112,Huang Shi13,Lindman Brian R.1112ORCID

Affiliation:

1. Department of Medicine Vanderbilt University Medical Center Nashville TN

2. Division of Cardiology Department of Medicine Stanford Medical Center Palo Alto CA

3. Division of Cardiology Department of Medicine Massachusetts General Hospital Boston MA

4. Division of Cardiology Department of Medicine Cleveland Clinic Foundation Cleveland OH

5. Division of Cardiology Department of Medicine University of Texas Southwestern Medical Center Dallas TX

6. Division of Cardiology Department of Medicine Morristown Medical Center Morristown NJ

7. Division of Cardiology Department of Medicine Intermountain Heart Institute Murray UT

8. Division of Cardiology Department of Medicine Barnes‐Jewish Hospital St. Louis MO

9. Division of Cardiology Department of Medicine University of Utah Hospital Salt Lake City UT

10. Department of Cardiovascular Medicine The Erlanger Heart and Lung Institute Chattanooga TN

11. Division of Cardiology Department of Medicine Vanderbilt University Medical Center Nashville TN

12. Structural Heart and Valve Center Vanderbilt University Medical Center Nashville TN

13. Department of Biostatistics Vanderbilt University School of Medicine Nashville TN

Abstract

Background Left ventricular hypertrophy (LVH) is associated with increased mortality risk and rehospitalization after transcatheter aortic valve replacement among those with severe aortic stenosis. Whether cardiac troponin (cTnT) and NT‐proBNP (N‐terminal pro‐B‐type natriuretic peptide) risk stratify patients with aortic stenosis and without LVH is unknown. Methods and Results In a multicenter prospective registry of 923 patients with severe aortic stenosis undergoing transcatheter aortic valve replacement, we included 674 with core‐laboratory‐measured LV mass index, cTnT, and NT‐proBNP. LVH was defined by sex‐specific guideline cut‐offs and elevated biomarker levels were based on age and sex cut‐offs. Adjusted Cox proportional hazards models evaluated associations between LVH and biomarkers and all‐cause death out to 5 years. Elevated cTnT and NT‐proBNP were present in 82% and 86% of patients with moderate/severe LVH, respectively, as compared with 66% and 69% of patients with no/mild LVH, respectively ( P <0.001 for each). After adjustment, compared with no/mild LVH, moderate/severe LVH was associated with an increased hazard of mortality (adjusted hazard ratio [aHR], 1.34; 95% CI 1.01–1.77, P =0.043). cTnT and NT‐proBNP each risk stratified patients with moderate/severe LVH ( P <0.05). In a model with both biomarkers and LVH included, elevated cTnT (aHR, 2.08; 95% CI 1.45–3.00, P <0.001) and elevated NT‐proBNP (aHR, 1.46; 95% CI 1.00–2.11, P =0.049) were each associated with increased mortality risk, whereas moderate/severe LVH was not ( P =0.15). Conclusions Elevations in circulating cTnT and NT‐proBNP are more common as LVH becomes more pronounced but are also observed in those with no/minimal LVH. As measures of maladaptive remodeling and cardiac injury, cTnT and NT‐proBNP predict post‐transcatheter aortic valve replacement mortality better than LV mass index. These findings may have important implications for risk stratification and treatment of patients with aortic stenosis.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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