Utilizing the improved receive sensitivity from high permittivity materials for SNR-challenged applications of ultrahigh b-factor diffusion-weighted spectroscopy at 7 Tesla
Carson Ingo1, Wyger M. Brink1, Andrew G. Webb1, and Itamar Ronen1

1C.J. Gorter Center for High Field MRI, Department of Radiology, Leiden University Medical Center, Leiden, Netherlands

Synopsis

Diffusion-weighted 7T MR spectroscopy in white matter regions of the brain using ultrahigh b-factors have established that intracellular metabolites exhibit non-Gaussian diffusion. Such measurements using b-factors well above 10,000 s/mm2 have inherently low SNR, and so it is crucial to optimize B1 sensitivity to ensure reliable results. Here we show that a single high permittivity pad can increase the receive sensitivity by ~30%, resulting in potential reductions in data acquisition time of ~70%.

Purpose

Metabolites such as total choline (tCho=choline+phosphocholine+glycerophosphocholine), total creatine (tCr=creatine+phosphocreatine), and total n-acetyl-aspartate (tNAA=NAA+NAAglutamate) are all intracellular, but reside within different axonal and glial cells1. Using high b-value diffusion-weighted spectroscopy (DWS), PCho, tCr, and tNAA have been shown to exhibit non-Gaussian diffusion (non-monoexponential signal decay) in the healthy human brain, although these metabolites are distributed differently among cellular microstructures2. For accurate characterization of metabolite diffusion in the intracellular space, DWS measurements require b-factors close to 20,000 s/mm2 and therefore suffer from relatively low SNR. Previous studies have shown that the increased transmit field efficiency using high permittivity materials enabled significant increases in spectral SNR in the medial temporal lobe at 7T, despite a reduced receive sensitivity produced by the dielectric pads3. In this study, we investigate the effects of designing dielectric pads to enhance the B1- receive sensitivity enhancements in parietal white matter, in particular for low SNR applications such as DWS at extremely high b-factors.

Methods

Seven healthy volunteers (25±4 years, 4 female, 3 male) were scanned on a 7T Philips Achieva MRI scanner. The pad (15x15x1 cm3, suspended barium titanate) was placed between the volunteer's head (positioned for the parietal volume) and the 32-channel receive channel coil as shown in Fig. 14. Local calibration of the transmit gain was performed by acquiring a whole-head B1+ map at a spatial resolution of 2.5x2.5x5 mm3 using the dual refocused acquisition mode (DREAM) sequence5,TR/TE = 4.5/1.8 ms. The B1+ field was calibrated within the spectroscopic VOI to produce 90° and 180° flip angles in the cases of both with and without the dielectric pad. The B1- receive sensitivity was first estimated using a 3D gradient-echo sequence with a tip angle of 1°, aligned with the DREAM geometry. Then, the ratio of the 3D gradient-echo image and the B1+ map yielded the receive sensitivity map in arbitrary units6,7.

Fig. 2a shows the 8 cm3 volume of interest (VOI) planned in the a) mostly parietal white matter (WM) for diffusion-weighted spectroscopy. The DWS data were acquired with a 13-interval STEAM sequence using bipolar diffusion gradients and cardiac synchronization8. Three orthogonal directions [1,1,-0.5], [1,-0.5,1], and [-0.5,1,1] were chosen to maximize the gradient strength for the isotropic diffusion weighting. DWS parameters were TR/TE=3000/105 ms, Δ=100 ms, δ=30 ms, τ=13 ms, and one gradient amplitude producing a b-factor of 17,794 s/mm2. The isotropic DWS data were eddy-current and phase corrected using custom Matlab codes as previously described9,10. The SNR was calculated by finding the individual peak intensities of PCho, tCr, and tNAA and comparing against the standard deviation of the residual spectra (i.e., frequency>6 ppm). The TE value was fixed at 105 ms for DWS measurements both without and with pad.

Results

Example B1- receive sensitivity maps without (Fig. 2b) and with pad (Fig. 2c), show an average improvement of ~34% within the locally power-optimized volume. Fig. 3 shows diffusion-weighted spectra (b=17,794 s/mm2), demonstrating an SNR increase of ~33-48% for the metabolites. Fig. 4 shows paired comparisons of DWS SNR improvement (p=0.0002) when using the high-permittivity pad. Fig. 5 shows the pad provided a clear increase in B1- sensitivity (p<0.0001) as well as a mild but significant decrease in B1+ variance within the localized volume (p=0.0148).

Discussion

Using a single dielectric pad, the SNR for DWS data acquired from the parietal lobe increased by more than 30%, which allows for a decrease in data acquisition time of ~70% for a given SNR4. Our results indicate the SNR boost is mostly due to increased receive sensitivity (closer coupling of the receive array to the head). The pad also provided slightly improved local B1 homogeneity (lower flip angle variability) within the DWS VOI, which also results in a higher SNR. The transmit efficiency within the VOI was increased using the dielectric pad, but since the RF pulses were calibrated separately without and with the pad, this did not impact the SNR: the slight increase in RF pulse length without the pad is irrelevant for DWS as TE is long (105 ms) and kept constant. However, for applications with short echo times (e.g., point-resolved MRS, TE~30 ms), the increased transmit efficiency due to the pad would improve SNR since TE can be further minimized, along with the added benefit of a reduced chemical shift displacement3.

Conclusion

For SNR-challenged local MR applications such as high b-factor DWS, high-permittivity materials significantly improve B1- sensitivity, allowing for robust in vivo measurements at ultrahigh b-factors in ultrafield systems that push the limits of current hardware capabilities.

Acknowledgements

This work has been funded by a grant from the Whitaker International Program of the Institute of International Education.

References

1. Ingo C, Ronen I, Webb AG. Anisotropy, Compartmentalization, and Anomalous Diffusion of Intracellular Metabolites in the Axons and Glia of the Human Brain at 7T. ISMRM. May 10-16 2014, Milan, Italy.

2. Wilhelmsson U, Bushong Ea, Price DL, Smarr BL, Phung V, Terada M, Ellisman MH, Pekny M. Redefining the concept of reactive astrocytes as cells that remain within their unique domains upon reaction to injury. PNAS. 2006;103(46):17,17513–17517.

3. Snaar JEM, Teeuwisse WM, Versluis MJ, van Buchem MA, Kan HE, Smith NB, and Webb AG. Improvements in high-field localized MRS of the medial temporal lobe in humans using new deformable high-dielectric materials. NMR Biomed. 2011;24,873–879.

4. Brink WM, van der Jagt AM, Versluis MJ, Verbist BM, Webb AG. High permittivity dielectric pads improve high spatial resolution magnetic resonance imaging of the inner ear at 7 T. Invest Radiol. 2014;49(5):271–277.

5. Nehrke K, Bornert P. DREAM-a novel approach for robust, ultrafast, multislice B1 mapping. Magn Reson Med. 2012;68(5):1517–1526.

6. Webb AG, Collins CM. Parallel transmit and receive technology in high-field magnetic resonance neuroimaging. Int J Imaging Syst Technol. 2010;20:2–13.

7. Brink WB, Webb AG. High Permittivity Pads Reduce Specific Absorption Rate, Improve B1 Homogeneity, and Increase Contrast-to-Noise Ratio for Functional Cardiac MRI at 3 T. Magn Reson Med. 2014;71:1632–1640.

8. Zheng G, Price WS. Suppression of background gradients in (B0 gradient-based) NMR diffusion experiments. Concept Magn Reson. 2007;30(5):261–277.

9. Kan HE, Techawiboonwong A, Van Osch MJP, Versluis MJ, Deelchand DK, Henry PG, Marjaska M, Van Buchem MA, Webb AG, Ronen I. Differences in apparent diffusion coefficients of brain metabolites between grey and white matter in the human brain measured at 7 T. Magn Reson Med. 2012;67(5):1203–1209.

10. Ronen I, Budde M, Ercan E, Annese J, Techawiboonwong A, Webb A. Microstructural organization of axons in the human corpus callosum quantified by diffusion- weighted magnetic resonance spectroscopy of N-acetylaspartate and post-mortem histology. Brain Struct Func. 2014;219(5):1773–1785.

Figures

Figure 1: example placement of the high permittivity pad in the 32-channel receive head coil to improve B1 sensitivity for ultrahigh b-factor diffusion weighted spectroscopy in the white matter of the parietal lobe.

Figure 2: example occipital, coronal, and transverse T1-weighted images for single volume DWS experiments planned in a) the mostly WM of the parietal lobe. B1- receive sensitivity maps are shown b) without the high permittivity pad and c) with the high permittivity pad.

Figure 3: example spectra in the non-Gaussian diffusion regime (b=17,794 s/mm2) a) without the high permittivity pad and b) with the high permittivity pad. The high permittivity pads improved SNR by 33.3% for tCho, 47.7% for tCr, and 36.8% for tNAA. Signals are normalized to the maximum tNAA signal for visual comparison.

Figure 4: SNR measures for tCho, tCr, and tNAA for the DWS data (left) and with (right) the high permittivity pad. The p-value is reported for a paired Students t-test.

Figure 5: measures for a) B1- receive sensitivity and b) B1+ % standard deviation within the planned volume without (left) and with (right) the high permittivity pad. The p-value is reported for a paired Students t-test.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
0743