Tissue-Based Predictors of Impaired Right Ventricular Strain in Coronary Artery Disease: A Multicenter Stress Perfusion Study

Author:

Villar-Calle Pablo1ORCID,Kochav Jonathan D.ORCID,Vadaketh Krista1ORCID,Chiu Caitlin1ORCID,Tak Katherine12,Agoglia Hannah1,Liberman Nicole1,Nguyen Kenny L.3ORCID,Vizcarra-Tellez Abdier4ORCID,Wu Alan5ORCID,RoyChoudhury Arindam5ORCID,Khalique Omar K.6,Judd Robert M.7,Kim Raymond J.78ORCID,Shah Dipan J.9ORCID,Heitner John F.10,Farzaneh-Far Afshin11,Shenoy Chetan12ORCID,Owyang Clark G.13ORCID,Mukherjee Monica14ORCID,Horn Evelyn M.1ORCID,Weinsaft Jonathan W.1,Kim Jiwon15ORCID

Affiliation:

1. Division of Cardiology (P.V.-C., K.V., C.C., K.T., H.A., N.L., E.M.H., J.W.W.), Weill Cornell Medicine, New York.

2. Division of Cardiology, University of Massachusetts Chan Medical School, Worcester (K.T.).

3. Department of Biomedical Engineering, Meinig School of Biomedical Engineering, Ithaca, NY (K.L.N.).

4. Division of Cardiology, Emergency Hospital of Villa El Salvador, Lima, Peru (A.V.-T.).

5. Division of Biostatistics and Epidemiology, Department of Population Health Sciences (A.W., A.R.C.), Weill Cornell Medicine, New York.

6. Division of Cardiac Imaging, Saint Francis Hospital and Catholic Health, Roslyn, NY (O.K.K.).

7. Department of Medicine (R.M.J., R.J.K.), Duke University Medical Center, Durham, NC.

8. Department of Radiology (R.J.K.), Duke University Medical Center, Durham, NC.

9. Houston Methodist De Bakey Heart & Vascular Center, TX (D.J.S.).

10. Division of Cardiology, New York University-Langone Health, New York (J.F.H.).

11. Division of Cardiology (A.F.-F.), Duke University Medical Center, Durham, NC.

12. Division of Cardiology, University of Minnesota Medical Center, Minneapolis (C.S.).

13. Pulmonary and Critical Care Medicine/Emergency Medicine (C.G.O.), Weill Cornell Medicine, New York.

14. Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD (M.M.).

15. Division of Cardiology, Columbia University Irving Medical Center, New York (J.K.).

Abstract

BACKGROUND: Right ventricular (RV) dysfunction is known to impact prognosis, but its determinants in coronary artery disease are poorly understood. Stress cardiac magnetic resonance (CMR) has been used to assess ischemia and infarction in relation to the left ventricle (LV); the impact of myocardial tissue properties on RV function is unknown. METHODS: Vasodilator stress CMR was performed in patients with known coronary artery disease at 7 sites between May 2005 and October 2018. Myocardial infarction was identified on late gadolinium enhancement-CMR, and infarct transmurality was graded on a per-segment basis. Ischemia was assessed on stress CMR based on first-pass perfusion and localized by using segment partitions corresponding to cine and late gadolinium enhancement analyses. RV function was evaluated by CMR-feature tracking for primary analysis with a global longitudinal strain threshold of 20% used to define impaired RV strain (RV IS ); secondary functional analysis via RV ejection fraction was also performed. RESULTS: A total of 2604 patients were studied, among whom RV IS was present in 461 patients (18%). The presence and magnitude of RV IS were strongly associated with LV dysfunction, irrespective of whether measured by LV ejection fraction or wall motion score ( P <0.001 for all). Regarding tissue substrate, regions of ischemic and dysfunctional myocardium (ie, hibernating myocardium) and infarct size were each independently associated with RV IS (both P <0.001). During follow-up (median, 4.62 [interquartile range, 2.15–7.67] years), 555 deaths (21%) occurred. Kaplan-Meier analysis for patients stratified by presence and magnitude of RV dysfunction by global longitudinal strain and RV ejection fraction each demonstrated strong prognostic utility for all-cause mortality ( P <0.001). RV IS conferred increased mortality risk (hazard ratio, 1.35 [95% CI, 1.11–1.66]; P =0.003) even after controlling for LV function, infarction, and ischemia. CONCLUSIONS: RV IS in patients with known coronary artery disease is associated with potentially reversible LV processes, including LV functional impairment due to ischemic and predominantly viable myocardium, which confers increased mortality risk independent of LV function and tissue substrate.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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