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Hypertrophic cardiomyopathy is associated with more severe left ventricular dyssynchrony than is hypertensive left
Toshiki Nagakura1, Masaaki Takeuchi, Hidetoshi Yoshitani
1Department of Cardiology and Internal Medicine, Tane General Hospital, Osaka, Japan.
Insights
Left ventricular hypertrophy (LVH) can cause left ventricular (LV) dyssynchrony. Hypertrophic cardiomyopathy (HCM) patients show more severe LV dyssynchrony than hypertensive heart disease (HHD) patients, potentially worsening cardiovascular outcomes.
Area of Science:
- Cardiology
- Medical Imaging
- Echocardiography
Background:
- Left ventricular hypertrophy (LVH) is a common cardiac condition.
- Distinguishing between hypertrophic cardiomyopathy (HCM) and hypertensive heart disease (HHD) is crucial for patient management.
- Left ventricular (LV) dyssynchrony may play a role in the pathophysiology of LVH.
Purpose of the Study:
- To evaluate left ventricular (LV) dyssynchrony in patients with LVH.
- To compare LV dyssynchrony in patients with HCM versus HHD.
- To utilize 2D speckle tracking imaging (STI) for assessing these abnormalities.
Main Methods:
- Acquired 2D LV short-axis images in 43 LVH patients (20 HCM, 23 HHD) and 15 controls.
- Measured radial and circumferential strain, and time to peak strain (Trs, Tcs) using 2D STI.
- Calculated LV dyssynchrony using the standard deviation of Trs/Tcs in 18 segments (Trs-18SD, Tcs-18SD).
Main Results:
- Regional strain was reduced in HCM compared to HHD, particularly in apical segments.
- LV dyssynchrony, measured by Trs-18SD and Tcs-18SD, was significantly longer in HCM patients.
- HCM patients exhibited more severe LV dyssynchrony (Trs-18SD: 88±32 ms, Tcs-18SD: 71±27 ms) than HHD (51±20 ms, 46±14 ms) and controls (45±12 ms, 45±14 ms).
Conclusions:
- LVH is not always associated with LV dyssynchrony.
- Severe LV dyssynchrony is characteristic of HCM.
- Increased LV dyssynchrony in HCM may contribute to adverse cardiovascular outcomes.
Objective:
To evaluate left ventricular (LV) dyssynchrony in patients with left ventricular hypertrophy (LVH), and to compare abnormalities associated with hypertrophic cardiomyopathy (HCM) and hypertensive heart disease (HHD) using 2D speckle tracking imaging.
Methods:
Basal, middle, and apical 2D LV short-axis images were acquired in 43 patients with LVH including 20 with HCM and 23 with HHD, and in 15 age-matched controls. Radial strain, circumferential strain, time interval from the R-wave to peak radial strain (Trs), and time to peak circumferential strain (Tcs) were measured in six equidistant segments at each level of the 3 LV short-axis views using 2D speckle tracking analysis. To assess LV dyssynchrony, Trs(cs)-18SD, the standard deviation (SD) of Trs(cs) in all 18 segments, was calculated.
Results:
Regional radial strain in the middle and apical short-axis segments was significantly less in patients with HCM than in those with HHD. Regional circumferential strain in the apical short-axis segments was also less in HCM. Trs-18SD and Tcs-18SD were significantly longer in patients with HCM than in age-matched controls and patients with HHD (Trs-18SD: HCM: 88 +/- 32 ms, HHD: 51 +/- 20 ms, control: 45 +/- 12 ms P < 0.001, Tcs-18SD: HCM: 71 +/- 27 ms, HHD: 46 +/- 14 ms, control: 45 +/- 14 ms P < 0.001).
Conclusions:
The presence of LVH is thus not always associated with LV dyssynchrony. However, the greater reduction of regional strain and severe LV dyssynchrony in HCM may contribute to the adverse cardiovascular outcomes associated with this disease.
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