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. 2023 Apr 17:e4951.
doi: 10.1002/nbm.4951. Online ahead of print.

Correction of errors in estimates of T at low spin-lock amplitudes in the presence of B0 and B1 inhomogeneities

Affiliations

Correction of errors in estimates of T at low spin-lock amplitudes in the presence of B0 and B1 inhomogeneities

Zhongliang Zu et al. NMR Biomed. .

Abstract

Relaxation rates R in the rotating frame measured by spin-lock methods at very low locking amplitudes (≤ 100 Hz) are sensitive to the effects of water diffusion in intrinsic gradients and may provide information on tissue microvasculature, but accurate estimates are challenging in the presence of B0 and B1 inhomogeneities. Although composite pulse preparations have been developed to compensate for nonuniform fields, the transverse magnetization comprises different components and the spin-lock signals measured do not decay exponentially as a function of locking interval at low locking amplitudes. For example, during a typical preparation sequence, some of the magnetization in the transverse plane is nutated to the Z-axis and later tipped back, and so does not experience R relaxation. As a result, if the spin-lock signals are fit to a monoexponential decay with locking interval, there are residual errors in quantitative estimates of relaxation rates R and their dispersion with weak locking fields. We developed an approximate theoretical analysis to model the behaviors of the different components of the magnetization, which provides a means to correct these errors. The performance of this correction approach was evaluated both through numerical simulations and on human brain images at 3 T, and compared with a previous correction method using matrix multiplication. Our correction approach has better performance than the previous method at low locking amplitudes. Through careful shimming, the correction approach can be applied in studies using low spin-lock amplitudes to assess the contribution of diffusion to R dispersion and to derive estimates of microvascular sizes and spacings. The results of imaging eight healthy subjects suggest that R dispersion in human brain at low locking fields arises from diffusion among inhomogeneities that generate intrinsic gradients on a scale of capillaries (~7.4 ± 0.5 μm).

Keywords: R1ρ fitting error; diffusion; low power; microvasculature; spin-lock; susceptibility gradients; vessel size.

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Figures

FIG. 1.
FIG. 1.
Diagram of spin-lock sequences with the conventional pulse (a) and the composite pulse preparation cluster (b).
FIG. 2.
FIG. 2.
(a) Schematic diagram to show the nutation of water magnetization (solid red arrow) about the effective field (dashed black arrow) in the first half of the composite pulse preparation cluster. Dashed red arrow shows the magnetization after the first 90x excitation pulse but before the spin-lock preparation cluster. (b) shows the instantaneous transverse component (light blue arrow) and the two residual longitudinal components: part 1 (purple arrow) and part 2 (green arrow) during the first half of the composite pulse preparation cluster. (c) shows the average transverse component (light blue arrow) and the part 1 of the residual longitudinal component (purple arrow) that tipped back into the transverse plane after the second half of the composite pulse preparation cluster. The black dotted arrows show the motion trajectory of the magnetization as well as their transverse and longitudinal components. Note that the part 1 of the residual longitudinal component in (b) and (c) are not necessarily to be equal.
FIG. 3.
FIG. 3.
Single-pool model simulated spin-lock signal vs. τ using the conventional rectangular (a, c) and the composite pulse (b, d) preparation cluster, respectively, at ω1 of 0 Hz (blue), 20 Hz (red), and 500 Hz (green). (a, b) show simulations with B0 shift (Δωoff=10Hz), but no B1 shift (β=1). (c, d) show simulations with no B0 shift (Δωoff=0Hz), but with B1 shift (β=0.9). Simulated spin-lock signals with no shifts in either B0 (Δωoff=0Hz) or B1 (β=1) with ω1 of 50 Hz (light blue) were also plotted in each subfigure as true spin-lock signals for comparison. The green and the light blue lines in (a) overlap. The blue, green, and light blue lines in (b) overlap. The red, green, and light blue lines in (d) overlap.
FIG. 4.
FIG. 4.
Spin-lock signals using the composite pulse preparation clusters vs. τ for the single-pool (a, c, e) and two-pool (b, d, f) models through numerical simulations (blue lines), calculated using our approximate formula Eq. (4) and Eq. (5) (red lines), as well as calculated using the rotation matrix multiplication approach (green lines) with ω1 of 20 Hz under B0 shifts (Δωoff=0 (dashed lines) and 10 Hz (solid lines), β=1),B1 shifts (β=1 (dashed lines) and 0.9 (solid lines), Δωoff=0Hz), and both B0 and B1 shifts (Δωoff=0 (dashed lines) and 10 Hz (solid lines), β=0.9). In all sub-figures, all dashed lines overlap. Corresponding residuals with the same colors (subtraction of the simulated data and the calculated data) are shown under each sub-figures.
FIG. 5.
FIG. 5.
Monte Carlo simulation of the R1ρ dispersions under B0 shift (a, b), B1 shift (c, d), and both B0 and B1 shift (e, f) without correction (blue line), corrected by approximate formula (red line), and corrected by matrix multiplication (green line) using the single-pool (a, c, e) and the two-pool (b, d, f) model. Simulations with no B0 and B1 shifts (black line) were also plotted for comparison. R1ρ values with ω1=0Hz and 10 Hz corrected by the matrix multiplication are not shown due to the large fitting uncertainty. The SNR of the added noise is 125. Simulations were performed with ω1 of 0, 10, 20, 30, 40, 50, 70, 80, 90, 100, 200, 300, 400, and 500Hz.
FIG. 6.
FIG. 6.
Relative change of the fitted R1ρ values under B0 and B1 shifts with/without correction using our approach from the true R1ρ values without B0 and B1 shifts (fittedR1ρtrueR1ρ/trueR1ρ) in the single-pool and two-pool model simulations.
FIG. 7.
FIG. 7.
Relative change of the fitted R1ρ values under B0 and B1 shifts with/without correction using the rotation matrix multiplication from the true R1ρ values without B0 and B1 shifts (fittedR1ρtrueR1ρ/trueR1ρ) in the single-pool and two-pool model simulations.
FIG. 8
FIG. 8
Simulated R1ρ dispersions obtained with a certain true B0 shift (i.e. Δωoff=10Hz,β=1) (a, b) and true B1 shift (i.e. Δωoff=0Hz,β=0.9) (c, d), but using a series of measured B0 shifts or B1 shifts which deviate from the true B0 and B1 shifts, respectively, for correction using our approximate formula.
FIG. 9
FIG. 9
Maps of T2 weighted anatomy (a), R1ρ with ω1 of 100 Hz (b), B0 shift (c), B1 shift (d), R without correction, with correction using the matrix multiplication, and with correction using our approximate formula (f, g, h), as well as g without correction, with correction using the matrix multiplication, and with correction using our approximate formula (i, j, k) from human subject #1. (e) shows the averaged R1ρ dispersions without correction, with correction using the matrix multiplication, and with correction using our approximate formula from the whole brain.

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