Shuang Leng1, Xiaodan Zhao1, Ru-San Tan1,2, Angela S. Koh1,2, Bryant Jennifer1, Jun-Mei Zhang1,2, Ris Low1, David Sim1,2, John C. Allen2, Hak Chiaw Tang1,2, and Liang Zhong1,2
1National Heart Centre Singapore, Singapore, Singapore, 2Duke-NUS Medical School, Singapore, Singapore
Synopsis
This study aimed to study the left ventricular
(LV) longitudinal deformation by a semi-automated and rapid assessable strain
parameter (i.e. global longitudinal strain, GLS) with standard cardiovascular magnetic
resonance images. Study population
consisted of 50 normal controls, 60 patients with heart failure (10 HFpEF,
10 HFmrEF and 40 HFrEF) and 10 patients with hypertrophic cardiomyopathy. Average processing
time of the fast strain measurement method was 78 ± 8 seconds per case
with intra- and inter-observer variations ranging from 3.3% to 5.8%. Results demonstrated that the fast and reproducible GLS is a powerful independent predictor in patients with HFpEF and HFmrEF.
Background and Purpose
Assessment of left
ventricular (LV) systolic longitudinal function has gained increasing
diagnostic and prognostic importance as an addition to LV ejection fraction
(EF) in patients with heart failure (HF) or hypertrophic cardiomyopathy (HCM).1 Strain imaging derived from speckle tracking echocardiography (STE) or feature
tracking cardiovascular magnetic resonance (FT-CMR) enables the direct
measurements of myocardial function in the longitudinal direction, however,
these parameters
often suffer from poor reproducibility and lack of the internal consistency. Therefore, there is unmet need
for an automated method that can assess the LV global longitudinal strain (GLS) rapidly and is reproducible.
Methods
This study enrolled
50 normal controls, and 70 patients (40 HF with reduced EF (HFrEF,
LVEF < 40%); 10 HF with mid-range EF (HFmrEF, LVEF 40 – 49%); 10 HF with
preserved EF (HFpEF, LVEF ≥ 50%); and 10 HCM). CMR scan was performed on a 3T
system (Ingenia, Philips Healthcare) using balanced turbo field echo sequence.
End-expiratory breath hold cine images were acquired in multi-planar long-axis
views including the two- and four-chamber views. Central off-line assessment of
LV volumes was performed using Simpson’s method; and longitudinal
LV strain parameters measured using an in-house semi-automatic post-processing
algorithm that tracked, on standard two- and four-chamber cine views, the
distance ($$$L$$$) between the left
atrioventricular junction and apical epicardium (Fig. 1A). The atrioventricular junctions were selected as the
mitral valve insertion points at the septal and lateral borders of the annulus
on the four-chamber view, and the anterior and inferior annular insertion
points on the two-chamber view.2-7 The strain of each wall at any
time point ($$$t$$$) in the cardiac
cycle from LV end-diastole ($$$t=0$$$) was calculated based on the strain formula: $$$\frac{\left(L(t)-L_{0}\right)\times100}{L_{0}}$$$. The peak systolic
GLS was obtained at $$$t$$$ equal to LV end-systole, and the corresponding
peak systolic strain rate (GLSR) was derived by taking the first-order
derivative of the strain (Fig. 1B). All
resulting values from the 4 walls in two- and four-chamber views were then
averaged to obtain the global GLS and GLSR of the whole LV. In addition, peak
mitral annular velocity during early systole (Sm) and systolic excursion
(MAPSE) were calculated based on the tracking of atrioventricular junction.2-5 Student’s t test or Mann-Whitney U test was used for inter-group
comparison; p < 0.05 denotes
statistical significance. The diagnostic performance of fast LV strain measurements for detecting HFpEF and HFmrEF was assessed using the receiver operating
characteristics (ROC) analysis.Results
The fast GLS
assessment was successfully performed in all cases and the average processing time was 78 ± 8 seconds per case. Intra- and inter-observer variations were ranging from 3.3% to 5.8% (all intra-class correlation coefficient (ICC) > 0.9). Compared with controls, a decreasing trend in GLS and GLSR was observed in patients with HCM, HFpEF, HFmrEF and HFrEF (GLS: normal, -16.9 ± 2.3%; HCM, -12.6 ± 2.5%; HFpEF, -11.8 ± 4.2%; HFmrEF, -10.3 ± 2.7%; HFrEF, -6.1 ± 2.4%; GLSR: normal,
-0.85 ± 0.15s-1; HCM,
-0.69 ± 0.13s-1; HFpEF,
-0.59 ± 0.16s-1; HFmrEF,
-0.55 ± 0.20s-1; HFrEF,
-0.34 ± 0.09s-1; p < 0.001, Table 1). On multivariate
analysis, fast LV GLS was found to be the independent predictor of HFpEF
and HFmrEF. The area under the ROC curve (AUC) in detecting HFpEF and HFmrEF compared with normal controls
(GLS < 14.0%) was 0.927 (sensitivity = 90%,
specificity = 88%, p < 0.001).
Conclusion
This study
demonstrated a fast, semi-automated, and robust GLS measurement method for
quantifying LV longitudinal function from routine cine CMR images without the
need for additional acquisition protocol
or special software tool. The fast GLS measurements had superior diagnostic
performance compared to conventional LV ejection fraction. In a population with
a high suspicion of HFpEF, GLS may significantly contribute to early diagnosis
and hence be useful in the triage and management of HFpEF and HFmrEF patients. Acknowledgements
This study received funding support from the National Medical Research Council of Singapore (NMRC/EDG/1037/2011; NMRC/TA/0031/2015; NMRC/OFIRG/0018/2016; NMRC/BnB/0017/2015), Hong Leong Foundation and Edwards Lifesciences.References
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