Daniela Franz1, Maximilian N. Diefenbach1, Jan Syväri1, Dominik Weidlich1, Ernst J. Rummeny1, Hans Hauner2, Stefan Ruschke1, and Dimitrios C. Karampinos1
1Ismaninger Str. 22, Department of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany, 2Else Kröner Fresenius Center for Nutritional Medicine, Technical University of Munich, Munich, Germany
Synopsis
PDFF and T2* have been previously proposed as two
important parameters in quantitative MRI of adipose tissue. This study investigates
the difference between gluteal and supraclavicular adipose tissue T2* and the
relationship between adipose tissue T2* and PDFF using a twenty-echo multi-echo
gradient echo acquisition. A highly significant difference between the PDFF in
different fat regions was detected in water-fat separation results when using
either the first 6 echoes or the full 20 echoes. However, T2* values were only
significantly different between fat regions, when using the full 20 echoes and
not when using the first 6 echoes. PDFF also correlated with T2* when using the
full 20 echoes.
Purpose
Adipose tissue can be
classified based on histological and functional properties as white, brown
or beige. Chemical shift encoding-based water-fat MRI techniques have gained
popularity in differentiating the compositional difference between white and
brown adipose tissue based on simultaneous mapping of the proton density fat
fraction (PDFF) and T2* [1]. Specifically, there have been multiple studies showing
that PDFF is lower in the frequently-brown-fat-containing supraclavicular fossa
compared to other white fat depots [2-7]. T2* has been also reported to be
lower in supraclavicular fat compared to other white fat depots [2-5]. However,
the range of adipose tissue T2* values reported in the literature for either
supraclavicular or white fat is relatively wide and primarily based on 6-echo
data [2-5]. Increasing the number of echoes in a multi-echo gradient echo
acquisition is expected to at least increase the precision of adipose tissue
T2* mapping. The purpose of this study was to investigate the difference
between gluteal and supraclavicular adipose tissue T2* and the relationship
between adipose tissue T2* and PDFF using a twenty-echo multi-echo gradient
echo acquisition.Methods
For this prospective study, 16 healthy subjects (10
females and 6 males; median BMI 22.7 kg/m2, range 17.2-44.5 kg/m2;
median age 40.7 years, range 22.5-63.1 years)
underwent an MRI of the neck and the abdomen/ pelvis on a 3T scanner (Ingenia,
Philips Healthcare). To measure the supraclavicular and gluteal PDFF,
a time-interleaved twenty-echo multi-echo gradient-echo sequence with monopolar
gradients was used: 2 interleaves, 10 echoes per interleaf, TR=24 ms, TE1=1.5 ms, ΔTE=1.0, flip angle=5°, bandwidth=961.5 Hz/pixel, FOV=400x300x140 mm³, 2 mm isotropic voxel size,
SENSE with R=2.5.
PDFF maps were generated using an off-line
complex-based water-fat separation routine accounting for known confounding
factors including the presence of multiple fat peaks (based on the previously
determined subcutaneous fat spectrum in [8]), a single T2* correction and phase
errors. The effect of concomitant gradients was corrected as in [9]. The water-fat
separation was performed once for the first 6 echoes and once for the full 20
echoes. For segmentation of the supraclavicular and subcutaneous fat, a
custom-built MATLAB-algorithm was used, delineating the deep supraclavicular
and gluteal subcutaneous fat pockets bilaterally (Figure 1 and 2). BMI was
calculated as weight in kg divided by height squared in m².Results
Both in the
6-echo-data and in the 20-echo-data, PDFF was significantly different in
supraclavicular vs. gluteal fat. With the 6-echo-data, PDFF was 78.4%
supraclavicular and 90.3% gluteal (p<0.0001). The 20-echo-data
resulted in a PDFF of 81.9% supraclavicular and 93.4% gluteal (p<0.0001)
(Figure 3). For T2*, a significant difference between supraclavicular and
gluteal fat was only visible in the 20-echo-dataset (20.9 ms
supraclavicular, 38.7 ms gluteal adipose tissue, p<0.0001) (Figure 4). Correlation
analyses showed a strong correlation between
PDFF and T2* in both supraclavicular and gluteal fat for the 20-echo-data (r=0.77, p<0.0001 supraclavicular and r=0.72, p<0.0001 gluteal) (Figure 5), but not for the 6-echo-data. Both PDFF and T2* of
supraclavicular and gluteal fat correlated with BMI for the 20-echo-data with r=0.5, p=0.004 for
supraclavicular T2*, r=0.37, p=0.03 for gluteal T2*, r=0.48, p=0.006 for
supraclavicular PDFF and r=0.38, p=0.03 for gluteal PDFF.Discussion & Conclusion
The present study shows a highly significant difference
between the PDFF in different fat regions for both 6- and 20-echo-data.
However, T2* values were only significantly different between fat depots in the
20-echo, but not the 6-echo-dataset. PDFF correlated with T2* for the
20-echo-dataset. Furthermore, BMI correlated with both PDFF and T2* for the
20-echo-dataset.
Therefore, the present findings suggest that adipose
tissue PDFF quantification is not affected by the number of sampled echoes,
whereas adipose tissue T2* is more significantly affected by the number of sampled
echoes. A 20-echo multi-echo gradient acquisition enables thus a
multi-parametric analysis of both adipose tissue PDFF and T2* and may improve
the MR-based differentiation between white and brown fat. Acknowledgements
The present work was
supported by the European Research Council (grant agreement No 677661 –
ProFatMRI) and Philips Healthcare.References
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