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Magnetic Resonance Derived Myocardial Strain Assessment Using Feature Tracking
Published on: February 12, 2011
CMR feature tracking strain patterns and their association with circulating cardiac biomarkers in patients with
Ersin Cavus1, Kai Muellerleile2, Samuel Schellert2
1Clinic of Cardiology, University Heart and Vascular Center Hamburg Eppendorf, Martinistr.52, 20246, Hamburg, Germany. ersin.cavus@uke.de.
Insights
Cardiovascular magnetic resonance feature tracking strain (CMR-FT) detects left ventricular and left atrial dysfunction in hypertrophic cardiomyopathy (HCM) even with normal ejection fraction. Impaired strain correlates with elevated biomarkers, suggesting subclinical dysfunction in HCM.
Area of Science:
- Cardiology
- Medical Imaging
- Biomarkers
Background:
- Cardiovascular magnetic resonance feature tracking strain (CMR-FT) offers prognostic insights.
- Data on CMR-FT in hypertrophic cardiomyopathy (HCM) is limited.
- Assessing global strain in all four cardiac chambers is crucial for understanding HCM.
Purpose of the Study:
- To analyze global CMR-FT parameters in all four cardiac chambers in HCM patients.
- To evaluate the association between CMR-FT parameters and NT-proBNP and cardiac troponin T (hsTnT) levels in HCM.
- To investigate subclinical cardiac dysfunction in HCM using CMR-FT.
Main Methods:
- Retrospective study of 144 HCM patients and 16 healthy controls using 1.5 T CMR.
- Analysis of standard steady-state free precession cine (SSFP) CMR data with commercial software.
- Global left ventricular (LV), right ventricular (RV), left atrial (LA), and right atrial (RA) strain assessed using feature tracking.
Main Results:
- Impaired LV longitudinal strain (LVLAX-GLS), LV short-axis radial strain (LVSAX-GRS), and LA longitudinal strain (LALAX-GLS) were observed in HCM patients compared to controls, despite normal LVEF.
- LV and LA strain parameters were further impaired in HCM patients with elevated NT-proBNP and/or hsTnT.
- Moderate correlations were found between LV and LA CMR-FT parameters and NT-proBNP/hsTnT levels.
Conclusions:
- CMR-FT effectively reveals LV and LA dysfunction in HCM, even when LVEF is preserved.
- The correlation between impaired strain and elevated biomarkers highlights a link between subclinical functional abnormalities and HCM severity.
- CMR-FT provides valuable insights into the functional cardiac status of HCM patients.
Aims:
CMR feature tracking strain (CMR-FT) provides prognostic information. However, there is a paucity of data in hypertrophic cardiomyopathy (HCM). We sought to analyze global CMR-FT parameters in all four cardiac chambers and to assess associations with NT-proBNP and cardiac troponin T (hsTnT) in patients with HCM.
Methods:
This retrospective study included 144 HCM patients and 16 healthy controls with CMR at 1.5 T. Analyses were performed on standard steady-state free precession cine (SSFP) CMR data using a commercially available software. Global left ventricular (LV) strain was assessed as longitudinal (LVLAX-GLS), circumferential (LVLAX-GCS) and radial strain (LVLAX-GRS) on long -axis (LAX) and as LVSAX-GCS and LVSAX-GRS on short- axis (SAX). Right ventricular (RV-GLS), left atrial (LA-GLS) and right atrial (RA-GLS) strain were assessed on LAX.
Results:
We found LVLAX-GLS [- 18.9 (- 22.0, - 16.0), - 23.5 (- 25.5, - 22.0) %, p = 0.0001), LVSAX-GRS [86.8 (65.9-115.5), 119.6 (91.3-143.7) %, p = 0.001] and LALAX-GLS [LA2CH-GLS 29.2 (19.1-37.7), LA2CH-GLS 38.2 (34.3-47.1) %, p = 0.0036; LA4CH-GLS 22.4 (14.6-30.7) vs. LA4CH-GLS 33.4 (28.4-37.3) %, p = 0.0033] to be impaired in HCM compared to healthy controls despite normal LVEF. Furthermore, LV and LA strain parameters were impaired in HCM with elevated NT-proBNP and/or hsTnT, despite preserved LVEF compared to HCM with normal biomarker levels. There was a moderate correlation of LV and LA CMR-FT with levels of NT-proBNP and hsTnT.
Conclusion:
CMR-FT reveals LV and LA dysfunction in HCM despite normal LVEF. The association between impaired LV strain and elevated NT-proBNP and hsTnT indicates a link between unapparent functional abnormalities and disease severity in HCM. Typical CMR-FT findings in patients with hypertrophic cardiomyopathy.
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