TY - JOUR
T1 - Proton nuclear magnetic resonance J-spectroscopy of phantoms containing brain metabolites on a portable 0.05 T MRI scanner
AU - Ronen, Itamar
AU - O'Reilly, Thomas
AU - Froeling, Martijn
AU - Webb, Andrew G
N1 - Funding Information:
We thank Dr. Pierre-Gilles Henry from the Center for Magnetic Resonance Research at the University of Minnesota for providing us with the simulation platform we used in this work. The work presented here was supported by the Simon Stevin Meester Prize awarded to A.G.W. (NWO grant # 14997 ).
Funding Information:
We thank Dr. Pierre-Gilles Henry from the Center for Magnetic Resonance Research at the University of Minnesota for providing us with the simulation platform we used in this work. The work presented here was supported by the Simon Stevin Meester Prize awarded to A.G.W. (NWO grant #14997).
Publisher Copyright:
© 2020 The Author(s)
PY - 2020/11
Y1 - 2020/11
N2 - We examined approaches for obtaining 1H NMR spectra of brain metabolites on a low-field (B0 = 0.05 T) portable MRI scanner, which was developed in our laboratory with the aim of bringing cost-effective radiological services to populations in underserved, remote regions. The low static magnetic field B0 dictates low signal to noise ratio for metabolites in the mM concentration range, and results in an overall spectral region for the 1H resonances of these metabolites narrower than the linewidth obtainable in our scanner. The narrow spectral range also precludes the possibility of suppressing the large contribution of the water resonance at the acquisition stage. We used a spectroscopic Carr-Purcell-Meiboom-Gill (CPMG) sequence to acquire multiecho data from solutions of J-coupled brain metabolites, focusing on lactic acid, a metabolite whose concentration is negligible in the healthy brain and increases significantly in several disease conditions. The J spectra we obtained for lactate from the Fourier transformation of the multiecho data are spectrally well-resolved for a range of echo spacing values. We show that the J spectra at different echo spacings fit well with simulations of the evolution of echo train signal of the lactate under the same conditions. Applying a J-refocused variant of the CPMG sequence, the J modulation of the echo decay is removed, providing a way for subtracting the large contribution of the non-modulated component in the J spectrum in conditions where notching it using post-processing methods is impossible. We also demonstrate by means of experimental data and simulations that in our experimental conditions, J-spectra of other prominent brain metabolites, such as the neurotransmitter glutamate, do not yield discernible peaks and only contribute to a broad peak at zero frequency.
AB - We examined approaches for obtaining 1H NMR spectra of brain metabolites on a low-field (B0 = 0.05 T) portable MRI scanner, which was developed in our laboratory with the aim of bringing cost-effective radiological services to populations in underserved, remote regions. The low static magnetic field B0 dictates low signal to noise ratio for metabolites in the mM concentration range, and results in an overall spectral region for the 1H resonances of these metabolites narrower than the linewidth obtainable in our scanner. The narrow spectral range also precludes the possibility of suppressing the large contribution of the water resonance at the acquisition stage. We used a spectroscopic Carr-Purcell-Meiboom-Gill (CPMG) sequence to acquire multiecho data from solutions of J-coupled brain metabolites, focusing on lactic acid, a metabolite whose concentration is negligible in the healthy brain and increases significantly in several disease conditions. The J spectra we obtained for lactate from the Fourier transformation of the multiecho data are spectrally well-resolved for a range of echo spacing values. We show that the J spectra at different echo spacings fit well with simulations of the evolution of echo train signal of the lactate under the same conditions. Applying a J-refocused variant of the CPMG sequence, the J modulation of the echo decay is removed, providing a way for subtracting the large contribution of the non-modulated component in the J spectrum in conditions where notching it using post-processing methods is impossible. We also demonstrate by means of experimental data and simulations that in our experimental conditions, J-spectra of other prominent brain metabolites, such as the neurotransmitter glutamate, do not yield discernible peaks and only contribute to a broad peak at zero frequency.
KW - Brain metabolites
KW - J-spectroscopy
KW - Low field MRI
KW - Magnetic Resonance Spectroscopy
UR - https://www.scopus.com/pages/publications/85091985767
U2 - 10.1016/j.jmr.2020.106834
DO - 10.1016/j.jmr.2020.106834
M3 - Article
C2 - 33022563
SN - 1090-7807
VL - 320
JO - Journal of Magnetic Resonance
JF - Journal of Magnetic Resonance
M1 - 106834
ER -