Why the study?
A better understanding of LV and RV function was needed to help differentiate between athlete's heart and dilated cardiomyopathy.
Can cardiac magnetic resonance feature tracking (CMR-FT) deformation parameters differentiate between athlete's heart, dilated cardiomyopathy, and sedentary healthy controls?
Can cardiac magnetic resonance feature tracking (CMR-FT) deformation parameters differentiate between athlete's heart, dilated cardiomyopathy, and sedentary healthy controls?
CMR-FT derived peak LV GRS diastolic rate and LVEF can accurately differentiate between physiological adaptation in endurance athletes and pathological changes in dilated cardiomyopathy.
A better understanding of the left ventricle (LV) and right ventricle (RV) functioning would help with the differentiation between athlete's heart and dilated cardiomyopathy (DCM). We aimed to analyse deformation parameters in endurance athletes relative to patients with DCM using cardiac magnetic resonance feature tracking (CMR-FT). The study included males of a similar age: 22 ultramarathon runners, 22 patients with DCM and 21 sedentary healthy controls (41 ± 9 years). The analysed parameters were peak LV global longitudinal, circumferential and radial strains (GLS, GCS and GRS, respectively); peak LV torsion; peak RV GLS. The peak LV GLS was similar in controls and athletes, but lower in DCM (p < 0.0001). Peak LV GCS and GRS decreased from controls to DCM (both p < 0.0001). The best value for differentiation between DCM and other groups was found for the LV ejection fraction (area under the curve (AUC) = 0.990, p = 0.0001, with 90.9% sensitivity and 100% specificity for ≤53%) and the peak LV GRS diastolic rate (AUC = 0.987, p = 0.0001, with 100% sensitivity and 88.4% specificity for >-1.27 s⁻¹). The peak LV GRS diastolic rate was the only independent predictor of DCM (p = 0.003). Distinctive deformation patterns that were typical for each of the analysed groups existed and can help to differentiate between athlete's heart, a nonathletic heart and a dilated cardiomyopathy.
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Małek et al. (2021) studied this question.
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