# Differentiation of Myocardial Properties in Physiological Athletic Cardiac Remodeling and Mild Hypertrophic Cardiomyopathy

**Authors:** Lars G. Klaeboe, Øyvind H. Lie, Pål H. Brekke, Gerhard Bosse, Einar Hopp, Kristina H. Haugaa, Thor Edvardsen

PMC · DOI: 10.3390/biomedicines12020420 · Biomedicines · 2024-02-12

## TL;DR

This study compares heart characteristics in athletes and people with mild hypertrophic cardiomyopathy using imaging techniques to help distinguish between the two conditions.

## Contribution

The study introduces the use of speckle tracking echocardiography and CMR to differentiate physiological athletic remodeling from mild HCM.

## Key findings

- Mechanical dispersion was significantly higher in HCM carriers compared to athletes.
- Native T1-time and extracellular volume differed significantly between the two groups.
- Native T1-time > 1230 ms identified all HCM carriers with high sensitivity and moderate specificity.

## Abstract

Clinical differentiation between athletes’ hearts and those with hypertrophic cardiomyopathy (HCM) can be challenging. We aimed to explore the role of speckle tracking echocardiography (STE) and cardiac magnetic resonance imaging (CMR) in the differentiation between athletes’ hearts and those with mild HCM. We compared 30 competitive endurance elite athletes (7% female, age 41 ± 9 years) and 20 mild phenotypic mutation-positive HCM carriers (15% female, age 51 ± 12 years) with left ventricular wall thickness 13 ± 1 mm. Mechanical dispersion (MD) was assessed by means of STE. Native T1-time and extracellular volume (ECV) were assessed by means of CMR. MD was higher in HCM mutation carriers than in athletes (54 ± 16 ms vs. 40 ± 11 ms, p = 0.001). Athletes had a lower native T1-time (1204 (IQR 1191, 1234) ms vs. 1265 (IQR 1255, 1312) ms, p < 0.001) and lower ECV (22.7 ± 3.2% vs. 25.6 ± 4.1%, p = 0.01). MD > 44 ms optimally discriminated between athletes and HCM mutation carriers (AUC 0.78, 95% CI 0.65–0.91). Among the CMR parameters, the native T1-time had the best discriminatory ability, identifying all HCM mutation carriers (100% sensitivity) with a specificity of 75% (AUC 0.83, 95% CI 0.71–0.96) using a native T1-time > 1230 ms as the cutoff. STE and CMR tissue characterization may be tools that can differentiate athletes’ hearts from those with mild HCM.

## Linked entities

- **Diseases:** hypertrophic cardiomyopathy (MONDO:0005045)

## Full-text entities

- **Diseases:** HCM (MESH:D002312)

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10886585/full.md

## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC10886585/full.md

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Source: https://tomesphere.com/paper/PMC10886585