Left Atrial Roof Enlargement Is a Distinct Feature of Heart Failure With Preserved Ejection Fraction

Author:

Backhaus Sören J.12ORCID,Nasopoulou Anastasia3ORCID,Lange Torben45,Schulz Alexander45,Evertz Ruben45ORCID,Kowallick Johannes T.56,Hasenfuß Gerd45,Lamata Pablo3ORCID,Schuster Andreas4578ORCID

Affiliation:

1. Department of Cardiology, Campus Kerckhoff of the Justus-Liebig-University Giessen, Kerckhoff-Clinic, Bad Nauheim, Germany (S.J.B.).

2. German Center for Cardiovascular Research (DZHK), Partner Site Rhine-Main, Bad Nauheim, Germany (S.J.B.).

3. Department of Biomedical Engineering, Division of Imaging Sciences and Biomedical Engineering, King’s College London, United Kingdom (A.N., P.L.).

4. Department of Cardiology and Pneumology, University Medical Center Göttingen, Georg-August University, Germany (T.L., A. Schulz, R.E., G.H., A. Schuster).

5. DZHK, Partner Site Lower Saxony, Germany (T.L., A. Schulz, R.E., J.T.K., G.H., A. Schuster).

6. FORUM Radiology, Rosdorf, Germany (J.T.K.).

7. FORUM Cardiology, Rosdorf, Germany (A. Schuster).

8. School of Biomedical Engineering and Imaging Sciences, King’s College London, United Kingdom (A. Schuster).

Abstract

BACKGROUND: It remains unknown to what extent intrinsic atrial cardiomyopathy or left ventricular diastolic dysfunction drive atrial remodeling and functional failure in heart failure with preserved ejection fraction (HFpEF). Computational 3-dimensional (3D) models fitted to cardiovascular magnetic resonance allow state-of-the-art anatomic and functional assessment, and we hypothesized to identify a phenotype linked to HFpEF. METHODS: Patients with exertional dyspnea and diastolic dysfunction on echocardiography (E/e′, >8) were prospectively recruited and classified as HFpEF or noncardiac dyspnea based on right heart catheterization. All patients underwent rest and exercise-stress right heart catheterization and cardiovascular magnetic resonance. Computational 3D anatomic left atrial (LA) models were generated based on short-axis cine sequences. A fully automated pipeline was developed to segment cardiovascular magnetic resonance images and build 3D statistical models of LA shape and find the 3D patterns discriminant between HFpEF and noncardiac dyspnea. In addition, atrial morphology and function were quantified by conventional volumetric analyses and deformation imaging. A clinical follow-up was conducted after 24 months for the evaluation of cardiovascular hospitalization. RESULTS: Beyond atrial size, the 3D LA models revealed roof dilation as the main feature found in masked HFpEF (diagnosed during exercise-stress only) preceding a pattern shift to overall atrial size in overt HFpEF (diagnosed at rest). Characteristics of the 3D model were integrated into the LA HFpEF shape score, a biomarker to characterize the gradual remodeling between noncardiac dyspnea and HFpEF. The LA HFpEF shape score was able to discriminate HFpEF (n=34) to noncardiac dyspnea (n=34; area under the curve, 0.81) and was associated with a risk for atrial fibrillation occurrence (hazard ratio, 1.02 [95% CI, 1.01–1.04]; P =0.003), as well as cardiovascular hospitalization (hazard ratio, 1.02 [95% CI, 1.00–1.04]; P =0.043). CONCLUSIONS: LA roof dilation is an early remodeling pattern in masked HFpEF advancing to overall LA enlargement in overt HFpEF. These distinct features predict the occurrence of atrial fibrillation and cardiovascular hospitalization. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03260621.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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