Reduced Ejection Fraction in Elite Endurance Athletes: Clinical and Genetic Overlap With Dilated Cardiomyopathy

Author:

Claessen Guido123ORCID,De Bosscher Ruben34,Janssens Kristel56,Young Paul7ORCID,Dausin Christophe8,Claeys Mathias3ORCID,Claus Piet3ORCID,Goetschalckx Kaatje4ORCID,Bogaert Jan910ORCID,Mitchell Amy M.5,Flannery Michael D.11,Elliott Adrian D.12,Yu Chenglong13ORCID,Ghekiere Olivier114,Robyns Tomas34ORCID,Van De Heyning Caroline M.1516,Sanders Prashanthan12ORCID,Kalman Jonathan M.1117ORCID,Ohanian Monique7,Soka Magdalena7,Rath Emma7ORCID,Giannoulatou Eleni7ORCID,Johnson Renee718ORCID,Lacaze Paul13ORCID,Herbots Lieven12,Willems Rik34ORCID,Fatkin Diane71819ORCID,Heidbuchel Hein1516ORCID,La Gerche André3571120,Van Soest Sofie,Bekhuis Youri,Pauwels Rik,De Paepe Jarne,Hespel Peter,Dymarkowski Steven,Dresselaers Tom,Miljoen Hielko,Favere Kasper,Paelinck Bernard,Vermeulen Dorien,Witvrouwen Isabel,Hansen Dominique,Op’t Eijnde Bert,Thijs Daisy,Vanvoorden Peter,Lefebvre Kristof,D’Ambrosio Paolo,Rowe Stephanie,Paratz Elizabeth,Brosnan Maria J.,Prior David L.

Affiliation:

1. Faculty of Medicine and Life Sciences, Limburg Clinical Research Center (LCRC), Hasselt University, Biomedical Research Institute, Diepenbeek, Belgium (G.C., O.G., L.H.).

2. Hartcentrum Hasselt (G.C., L.H.), KU Leuven, Belgium.

3. Jessa Ziekenhuis, Belgium. Department of Cardiovascular Sciences (G.C., R.D.B., M.C., P.C., T.R., R.W., A.L.G.), KU Leuven, Belgium.

4. Department of Cardiovascular Diseases (R.D.B., K.G., T.R., R.W.), University Hospitals Leuven, Belgium.

5. HEART (Heart Exercise and Research Trials) Lab, St Vincent’s Institute of Medical Research, Fitzroy, Australia (K.J., A.M.M., A.L.G.).

6. Exercise and Nutrition Research Program, The Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne Australia (K.J.).

7. Victor Chang Cardiac Research Institute, Darlinghurst, Australia (P.Y., M.O., M.S., E.R., E.G., R.J., D.F., A.L.G.).

8. Department of Movement Sciences (C.D.), KU Leuven, Belgium.

9. Department of Imaging and Pathology (J.B.), KU Leuven, Belgium.

10. Department of Radiology (J.B.), University Hospitals Leuven, Belgium.

11. Department of Medicine, University of Melbourne, Parkville, Australia (M.D.F., J.M.K., A.L.G.).

12. Centre for Heart Rhythm Disorders, University of Adelaide and Royal Adelaide Hospital, Australia (A.D.E., P.S.).

13. Department of Epidemiology and Preventive Medicine, School of Public Health and Preventive Medicine, Monash University, Melbourne, Australia (C.Y., P.L.).

14. Department of Radiology (O.G.), KU Leuven, Belgium.

15. Department of Cardiovascular Sciences, University of Antwerp, Belgium (C.M.V.D.H., H.H.).

16. Department of Cardiology, University Hospital Antwerp, Belgium (C.M.V.D.H., H.H.).

17. Department of Cardiology, Royal Melbourne Hospital, Australia (J.M.K.).

18. School of Clinical Medicine, Faculty of Medicine and Health, UNSW Sydney, Kensington, Australia (R.J., D.F.).

19. Cardiology Department, St Vincent’s Hospital, Darlinghurst, Australia (D.F.).

20. Cardiology Department, St Vincent’s Hospital Melbourne, Fitzroy, Australia (A.L.G.).

Abstract

BACKGROUND: Exercise-induced cardiac remodeling can be profound, resulting in clinical overlap with dilated cardiomyopathy, yet the significance of reduced ejection fraction (EF) in athletes is unclear. The aim is to assess the prevalence, clinical consequences, and genetic predisposition of reduced EF in athletes. METHODS: Young endurance athletes were recruited from elite training programs and underwent comprehensive cardiac phenotyping and genetic testing. Those with reduced EF using cardiac magnetic resonance imaging (defined as left ventricular EF <50%, or right ventricular EF <45%, or both) were compared with athletes with normal EF. A validated polygenic risk score for indexed left ventricular end-systolic volume (LVESVi-PRS), previously associated with dilated cardiomyopathy, was assessed. Clinical events were recorded over a mean of 4.4 years. RESULTS: Of the 281 elite endurance athletes (22±8 years, 79.7% male) undergoing comprehensive assessment, 44 of 281 (15.7%) had reduced left ventricular EF (N=12; 4.3%), right ventricular EF (N=14; 5.0%), or both (N=18; 6.4%). Reduced EF was associated with a higher burden of ventricular premature beats (13.6% versus 3.8% with >100 ventricular premature beats/24 h; P =0.008) and lower left ventricular global longitudinal strain (–17%±2% versus –19%±2%; P <0.001). Athletes with reduced EF had a higher mean LVESVi-PRS (0.57±0.13 versus 0.51±0.14; P =0.009) with athletes in the top decile of LVESVi-PRS having an 11-fold increase in the likelihood of reduced EF compared with those in the bottom decile ( P =0.034). Male sex and higher LVESVi-PRS were the only significant predictors of reduced EF in a multivariate analysis that included age and fitness. During follow-up, no athletes developed symptomatic heart failure or arrhythmias. Two athletes died, 1 from trauma and 1 from sudden cardiac death, the latter having a reduced right ventricular EF and a LVESVi-PRS >95%. CONCLUSIONS: Reduced EF occurs in approximately 1 in 6 elite endurance athletes and is related to genetic predisposition in addition to exercise training. Genetic and imaging markers may help identify endurance athletes in whom scrutiny about long-term clinical outcomes may be appropriate. REGISTRATION: URL: https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=374976&isReview=true ; Unique identifier: ACTRN12618000716268.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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