Anoop Ayyappan1, Harshith Kramadhari1, Ajit Kumar1, and Kapilamoorthy T.R.1
1Department of IS & IR, Sree Chitra Tirunal Institute of Medical Sciences & Technology, Kerala, India
Synopsis
Hypertrophic cardiomyopathy (HCM) is a disorder of myocardium having a genetic basis, and high disease related mortality. Identification of areas of occult fibrosis along with overt fibrosis using T1 mapping will be useful in long term prognosis of patients along with other imaging parameters in MRI. This study was aimed at (a) determining the differences in native T1 values of controls and HCM patients, (b) to determine the relationship between early gadolinium enhancement (EGE)/Late gadolinium enhancement (LGE)/ perfusion abnormalities and native T1 and ECV values in patients of hypertrophic cardiomyopathy.
Aims and objectives
This study was aimed at (a)
determining the differences in native T1 values of controls and HCM patients,
(b) to determine the relationship between early gadolinium enhancement
(EGE)/Late gadolinium enhancement (LGE) and native T1 values & ECV in
patients of hypertrophic cardiomyopathy.Materials and methods
The
study included 33 patients of HCM and 9 matched controls. CMR was done on 3T
MRI machine (MR750w,
GE Healthcare, Waukesha, WI, USA)
with cardiac gating. SMART T1 (Native T1 mapping was acquired from saturation
pulses with different delay times [300, 600 ms] and without magnetization preparation.
Imaging parameters: Repetition time 3.9 ms; Echo time 1.8 ms; Flip angle 45°; Section
thickness 8 mm; Field of- view 360 mm; Matrix size 192 × 128. TI – 250 - 20000
ms.8 datasets were obtained over 14 heartbeats which are shown in the Figure 1)
maps were created by the MR system and were used to assess the native T1 values
of the heart for all the 16 segments of the heart according to the AHA model.
Perfusion assessment, EGE and LGE quantification was done using the Cvi 42
software. A subset (n=13) of these patients had ECV mapping assessed by manual
calculation.Results
Native
T1 values were higher in the HCM patient compared to the matched controls
(1538.67 + 93 ms vs 1458.75 + 43 ms) and was statistically significant (p=<
0.05). ROC curve showed AUC of 0.78 with a cutoff of 1485.5 ms showing 77 %
sensitivity and 79 % specificity at differentiating normal myocardium from HCM
patients. The native T1 values were longer in areas of the heart in HCM
patients with perfusion defects (1570.62 ± 78 ms vs 1535.25 ± 95 ms), was not
statistically significant. The native T1 values were longer in segments showing
EGE (1541.71 ± 103ms vs 1532.64 ± 86 ms), which was significant (p = <
0.05). Comparison of native T1 values and LGE showed longer T1 times in the
segments showing LGE (Figure 2) when compared to segments without LGE (1554.79 ±94
ms vs 1533.63 ± 94 ms), which was not statistically significant. We observed a
positive correlation between maximum wall thickness and native T1 values, which
was statistically significant (p=< 0.01). ECV values were higher in cases
with scar compared to cases without scar (61% vs 40 %) but was not
statistically significant because of low number of patients (n=13).Conclusion
Native
T1 values of myocardium by SMART1 maps can differentiate normal myocardium from
cases of HCM, however there was significant overlap in values from both the
group. It can detect areas of myocardial fibrosis which can go undetected by
LGE and myocardial edema. However, T1 mapping can only be used as an adjunct to
EGE and LGE sequences. T1 mapping can predict disease burden, as the T1 values
increased with increase in the myocardial thickness.Acknowledgements
The authors would like to acknowledge GE
Healthcare for their research support.References
No reference found.