Skip to main content
Elsevier Sponsored Documents logoLink to Elsevier Sponsored Documents
. 2021 Nov 1;241:118430. doi: 10.1016/j.neuroimage.2021.118430

Frequency drift in MR spectroscopy at 3T

Steve CN Hui a,b, Mark Mikkelsen a,b, Helge J Zöllner a,b, Vishwadeep Ahluwalia c, Sarael Alcauter d, Laima Baltusis e, Deborah A Barany f, Laura R Barlow g, Robert Becker h, Jeffrey I Berman i, Adam Berrington j, Pallab K Bhattacharyya k, Jakob Udby Blicher l, Wolfgang Bogner m, Mark S Brown n, Vince D Calhoun o, Ryan Castillo p, Kim M Cecil q, Yeo Bi Choi r, Winnie CW Chu s, William T Clarke t, Alexander R Craven u, Koen Cuypers v,aq, Michael Dacko w, Camilo de la Fuente-Sandoval x, Patricia Desmond y, Aleksandra Domagalik z, Julien Dumont aa, Niall W Duncan ab, Ulrike Dydak ac, Katherine Dyke ad, David A Edmondson q, Gabriele Ende h, Lars Ersland ae, C John Evans af, Alan SR Fermin ag, Antonio Ferretti ah, Ariane Fillmer ai, Tao Gong aj, Ian Greenhouse ak, James T Grist al, Meng Gu am, Ashley D Harris an, Katarzyna Hat z1, Stefanie Heba ao, Eva Heckova m, John P Hegarty II ap, Kirstin-Friederike Heise aq, Shiori Honda cp, Aaron Jacobson ar, Jacobus FA Jansen as, Christopher W Jenkins af, Stephen J Johnston at, Christoph Juchem au, Alayar Kangarlu av, Adam B Kerr e, Karl Landheer au, Thomas Lange w, Phil Lee aw, Swati Rane Levendovszky ax, Catherine Limperopoulos ay, Feng Liu av, William Lloyd az, David J Lythgoe ba, Maro G Machizawa ag, Erin L MacMillan g,cm, Richard J Maddock bb, Andrei V Manzhurtsev bc,bu, María L Martinez-Gudino bd, Jack J Miller be,co, Heline Mirzakhanian ar, Marta Moreno-Ortega av, Paul G Mullins bf, Shinichiro Nakajima cp, Jamie Near bg, Ralph Noeske cn, Wibeke Nordhøy bh, Georg Oeltzschner a,b, Raul Osorio-Duran bd, Maria CG Otaduy bi, Erick H Pasaye d, Ronald Peeters bj, Scott J Peltier bk, Ulrich Pilatus bl, Nenad Polomac bl, Eric C Porges bm, Subechhya Pradhan ay, James Joseph Prisciandaro bn, Nicolaas A Puts bo, Caroline D Rae p, Francisco Reyes-Madrigal x, Timothy PL Roberts i, Caroline E Robertson r, Jens T Rosenberg bp, Diana-Georgiana Rotaru ba, Ruth L O'Gorman Tuura bq, Muhammad G Saleh br, Kristian Sandberg l, Ryan Sangill l, Keith Schembri bs, Anouk Schrantee bt, Natalia A Semenova bc,bu, Debra Singel bv, Rouslan Sitnikov bw, Jolinda Smith bx, Yulu Song aj, Craig Stark by, Diederick Stoffers bz, Stephan P Swinnen aq, Rongwen Tain by, Costin Tanase bb, Sofie Tapper a,b, Martin Tegenthoff ao, Thomas Thiel ca, Marc Thioux cb, Peter Truong cc, Pim van Dijk cb, Nolan Vella bs, Rishma Vidyasagar cd, Andrej Vovk ce, Guangbin Wang aj, Lars T Westlye bh, Timothy K Wilbur ax, William R Willoughby cf, Martin Wilson cg, Hans-Jörg Wittsack ch, Adam J Woods bm, Yen-Chien Wu ci, Junqian Xu cj, Maria Yanez Lopez ck, David KW Yeung s, Qun Zhao cl, Xiaopeng Zhou ac, Gasper Zupan ce, Richard AE Edden a,b,
PMCID: PMC8456751  PMID: 34314848

Abstract

Purpose

Heating of gradient coils and passive shim components is a common cause of instability in the B0 field, especially when gradient intensive sequences are used. The aim of the study was to set a benchmark for typical drift encountered during MR spectroscopy (MRS) to assess the need for real-time field-frequency locking on MRI scanners by comparing field drift data from a large number of sites.

Method

A standardized protocol was developed for 80 participating sites using 99 3T MR scanners from 3 major vendors. Phantom water signals were acquired before and after an EPI sequence. The protocol consisted of: minimal preparatory imaging; a short pre-fMRI PRESS; a ten-minute fMRI acquisition; and a long post-fMRI PRESS acquisition. Both pre- and post-fMRI PRESS were non-water suppressed. Real-time frequency stabilization/adjustment was switched off when appropriate. Sixty scanners repeated the protocol for a second dataset. In addition, a three-hour post-fMRI MRS acquisition was performed at one site to observe change of gradient temperature and drift rate. Spectral analysis was performed using MATLAB. Frequency drift in pre-fMRI PRESS data were compared with the first 5:20 minutes and the full 30:00 minutes of data after fMRI. Median (interquartile range) drifts were measured and showed in violin plot. Paired t-tests were performed to compare frequency drift pre- and post-fMRI. A simulated in vivo spectrum was generated using FID-A to visualize the effect of the observed frequency drifts. The simulated spectrum was convolved with the frequency trace for the most extreme cases. Impacts of frequency drifts on NAA and GABA were also simulated as a function of linear drift. Data from the repeated protocol were compared with the corresponding first dataset using Pearson's and intraclass correlation coefficients (ICC).

Results

Of the data collected from 99 scanners, 4 were excluded due to various reasons. Thus, data from 95 scanners were ultimately analyzed. For the first 5:20 min (64 transients), median (interquartile range) drift was 0.44 (1.29) Hz before fMRI and 0.83 (1.29) Hz after. This increased to 3.15 (4.02) Hz for the full 30 min (360 transients) run. Average drift rates were 0.29 Hz/min before fMRI and 0.43 Hz/min after. Paired t-tests indicated that drift increased after fMRI, as expected (p < 0.05). Simulated spectra convolved with the frequency drift showed that the intensity of the NAA singlet was reduced by up to 26%, 44 % and 18% for GE, Philips and Siemens scanners after fMRI, respectively. ICCs indicated good agreement between datasets acquired on separate days. The single site long acquisition showed drift rate was reduced to 0.03 Hz/min approximately three hours after fMRI.

Discussion

This study analyzed frequency drift data from 95 3T MRI scanners. Median levels of drift were relatively low (5-min average under 1 Hz), but the most extreme cases suffered from higher levels of drift. The extent of drift varied across scanners which both linear and nonlinear drifts were observed.

Keywords: Magnetic resonance spectroscopy (MRS), Frequency drift, 3T, Press, Multi-vendor, Multi-site

1. Introduction

MRI scanners rely upon a strong magnetic field (B0) in order to polarize the bulk magnetization of 1H protons and generate detectable radiofrequency (RF) signals. Magnetic field gradient pulses allow the encoding of position as the resonance frequency is linearly proportional to the magnetic field. Hence, gradient pulses are used to make RF pulses slice-selective, to suppress unwanted signals, and to directly read out the location of signals during acquisition. Rapid switching of gradient fields, which is a common feature of efficient modern imaging sequences, results in the deposition of substantial amounts of energy within the scanner. Eddy currents release heat between vibrating parts in the coil system, heating up the nearby heat shield and shimming elements (El-Sharkawy et al., 2006; Foerster et al., 2005). Although the gradient coils themselves are water-cooled, vibrations and eddy currents that they induce deposit energy elsewhere in the scanner that is less efficiently temperature-controlled, changing the local temperature of conducting scanner components. Unstable internal temperature leads to temperature-dependent changes in magnetic susceptibility and thus the B0 field (Foerster et al., 2005).

Instability in the B0 magnetic field can impact experiments in several ways. Firstly, experiments often rely upon frequency-selective pulses, including for positional and chemical-shift selectivity. Secondly, detected signals will be distorted by short-term B0 instabilities during the acquisition window. Thirdly, longer-term B0 instabilities will interfere with the appropriate combination of signals acquired during different TRs. Typically, slice-selective pulses are applied with high bandwidth and the location of signals is only minimally shifted by B0 instability. In time-series fMRI, significant SNR loss due to gradient-induced heat drift can be recovered by realignment correction (Lange et al., 2011). However, MR spectroscopy (MRS) and imaging applications, which include chemical exchange saturation transfer imaging (CEST) and lipid suppression, make use of chemical-shift-selective pulses of narrower bandwidth, and hence will be more adversely impacted by B0 instability (Poblador Rodriguez et al., 2019). Thus, B0 instability particularly impacts MRS experiments, which rely upon extensive signal averaging, leading to incoherent averaging, line-broadened, distorted peaks and reduced SNR (Foerster et al., 2005; Henry et al., 1999; Rowland et al., 2017).

The magnitude of gradient-induced B0 field changes varies depending on the length of the applied imaging protocol and the gradient duty cycle of the sequences, particularly when echo planar imaging (EPI) is used for e.g. fMRI and diffusion tensor imaging (DTI). In addition, scanner design characteristics including the amount and distribution of iron used in the passive shim elements plays a role in the B0 field changes (Lange et al., 2011). It has been reported that up to ten hours were required for B0 to return to its initial value after a two-hour fMRI acquisition (Foerster et al., 2005). B0 field drift changes have a particular impact on J-difference approaches that rely on alignment and subtraction of individual transients, as is the case for e.g. MEGA–editing of GABA. One study reported frequency drift rates of over 1 Hz/min after 8 min of fMRI (Harris et al., 2014), compared to under 0.1 Hz/min without prior imaging and showed drift was associated with a 16% decrease in the GABA+ signal as measured with the respective edited MRS acquisition. This change in metabolite signal can be explained by the shifted position of frequency-selective editing pulses that characterize editing, targeting the scalar-coupled GABA resonances at 1.89 ppm and measurement of the observed signal at 3.01 ppm (Edden et al., 2012). A comparable field drift has also been observed after a 22- minute DTI acquisition, which resulted in an over 3 Hz/min drift after DTI compared to under 1 Hz/min without a previous DTI scan (Rowland et al., 2017). The narrow bandwidth of editing pulses makes frequency drift influential on both the efficiency of the editing experiment and the summation and subtraction of sub-spectra (Edden and Barker, 2007; van der Veen et al., 2017).

Given the particular impact of field drift on MRS, much work has sought to mitigate the impact of field drift on data through both prospective and retrospective approaches. The line-broadening and SNR losses caused by incoherent averaging of signals acquired with different B0 frequencies can be addressed to a large extent by retrospective frequency correction during post-processing, which is now a consensus-recommended step in all MRS processing (Near et al., 2020; Wilson et al., 2019). Corrections via residual water signals, creatine referencing, spectral registration and non-water-suppressed methods have comparable efficacy on frequency correction (Ernst and Li, 2011; Helms and Piringer, 2001; Keating and Ernst, 2012; Near et al., 2015; van der Veen et al., 2017; Waddell et al., 2007; Wilson, 2019). In the residual water method, frequency shift and phase offset are corrected using the maximum water modulus and phase of the first point in the FID. In creatine referencing, the creatine peak is fitted to the real part of a Lorentzian using global nonlinear least squares with constrained parameters to achieve frequency and phase alignment. Spectral registration uses a representative average as a reference and fits other signal averages to this reference in the time domain using nonlinear least squares minimization. Non-water-suppressed acquisition techniques such as metabolite cycling offer the ability to improve frequency alignment in post-processing steps by aligning the high SNR water peak in each transient, but these acquisition methods have yet to be incorporated as product on clinical MRI systems. Nonetheless, many negative impacts of B0 field drift cannot be removed by post-processing.

Prospective approaches such as a feedback-based interleaved reference scan (IRS) method utilize the water reference signal for a real‐time update of the carrier frequency of RF pulses and analog-to-digital converter (Edden et al., 2016; Henry et al., 1999; Lange et al., 2011; Thiel et al., 2002). This feedback mechanism updates the water resonance on the basis of individual transients to prevent the water resonance from drifting in order to achieve drift correction. The IRS-based method has also been implemented in MRS imaging sequences for field drift and localization error correction (Ebel and Maudsley, 2005; Tal and Gonen, 2013). A more recent study proposed to obtain a localized reference using outer volume suppression localization and selective water excitation (Lee et al., 2018). This method prevents the saturation-induced SNR loss that happens in PRESS-based IRS navigators while also using the water peak as the reference for frequency drift correction. Difference-edited MRS, which relies upon accurate subtraction of large signals to resolve smaller ones, is particularly impacted by field drift, and the elimination of subtraction artifacts is an enduring challenge (Evans et al., 2013; Near et al., 2020; Waddell et al., 2007; Wilson et al., 2019). Water suppression pulses are often applied with narrow bandwidths in order to preserve signals around 4 ppm, and the size of the residual water signal can change dramatically after drift. The use of frequency-selective pulses is even more integral to edited MRS methods (Mullins et al., 2014), and if the resonant frequency of signals drifts away from the nominal frequency of editing pulses, losses in editing efficiency arise.

Frequency drift during either MRS or EPI-based acquisitions has rarely been studied especially on a large-scale multi-site and multi-vendor manner. Published works are mostly single-site and single-scanner studies which may not be representative to other scanners due to the use of different protocols and study design (Foerster et al., 2005; Harris et al., 2014; Rowland et al., 2017). The amount of frequency drift is scanner-dependent and related to the scanner's gradient coil system and cooling hardware that may vary across scanners. Such impact of drift may be reduced using prospective or retrospective frequency correction methods. However, efficacy of such corrections is poorly characterized and the impact of line-broadening, lineshape distortion, subtraction artifacts, and accuracy of frequency-selective pulses on spectral data collected from multiple scanners remains unclear. In this study, a standardized protocol was developed and shared across different sites with scanners from various vendors to study the impact of gradient-induced frequency drift and the consistency of drift within scanner. The aim of the standardized protocol was to reduce the number of confounding variables, allowing objective analysis of how EPI scanning influences frequency drift and how this may impact MR spectral analysis. By collecting data from a large number of sites worldwide, we aimed to establish a benchmark of the ‘typical’ levels of drift and to assess the need for real-time field-frequency locking (Henry et al., 1999). Each acquired dataset consisted of two sets of PRESS scans immediately before and after an EPI acquisition to characterize the B0 field drift.

2. Methods

2.1. Scanner details

Site recruitment was initiated from previous multi-site studies involving imaging centers focusing on neurological and psychological research with 3T scanners worldwide (Mikkelsen et al., 2017; Mikkelsen et al., 2019), and subsequently extended through advertising on social media. Eighty sites with 99 scanners were recruited (GE = 22, Philips = 30, Siemens = 47) and supplied data, of which 60 sites submitted two datasets acquired on separate days. Four sites with PET/MR scanners participated. See Table 1 for details.

Table 1.

Number of participating sites and data reported.

Sites Data reported (excluded) Repeated data*
GE 21 22 (1) 15
Philips 23 30 (0) 20
Siemens 36 47 (3) 25
Total 80 99 (4) 60

No repeated data were excluded.

2.2. Data acquisition

Sites were instructed to use a spherical or cylindrical water-dominant phantom, and a phased-array head or head-and-neck RF coil (between 8 and 64 channels). Scanning was performed following a period of at least 6h of scanner idle time (ideally the first scan of the day) to avoid any drift confounds due to unintended heating effects from prior scanning. Phantoms were acclimatized in the scan room for the same period and positioned in the isocenter. Each site was required to submit a minimum of one dataset and suggested to repeat the protocol on a different day for a second dataset if possible. Phantom data files were shared securely and analyzed by the co-authors at the Johns Hopkins University School of Medicine with local IRB approval.

Raw data were exported in GE P-file (.7), Philips .data/.list and SDAT/SPAR and Siemens TWIX (.dat) formats as these formats contain the unaveraged information and, hence, allow for frequency and phase of individual transients to be observed. Data were uploaded to a secure online repository. Scanner details (i.e., date of scan, scanner vendor and model, software version, year of installation, estimated hours of use per day, coil, maximum gradient amplitude and gradient slew rate) were reported. Additional metrics including the course of the gradient temperature during the experiment and the number and bulk weight of passive shims were suggested to be included if available.

2.3. Scanning protocol

Unsuppressed water data were acquired from the phantom, using PRESS localization with real-time frequency stabilization/adjustment switched off, before and after a BOLD-weighted fMRI sequence. Standardized protocols were generated for GE, Philips and Siemens scanners consisting of: 1) minimal preparatory imaging; 2) pre-fMRI PRESS (TR/TE = 5000/35 ms; FA = 90°; 64 transients; no water suppression; voxel size = 2 × 2 × 2 cm3; second-order shim; scan duration = 5:20 min); 3) BOLD-weighted EPI based on the ADNI-3 protocol (Weiner et al., 2017) (TR/TE = 3000/30 ms; 197 dynamics; EPI factor/echo train length = 31/64, Inter-echo times (echo spacing) 0.5 ms (GE and Philips) / 0.72 ms (Siemens) and FOV = 217×217 mm2 (Philips and Siemens) / 220×220 mm2 (GE), duration = 10 min); and 4) post-fMRI PRESS (same parameters as for pre-fMRI PRESS except 360 transients and duration = 30 min).

In addition, one GE site repeated the protocol with an extra-long acquisition, consisting of 16-min pre-fMRI PRESS (192 transients) and 171-minute post-fMRI PRESS (2048 transients) to investigate the time required for the frequency offset to reach a plateau. Except for the number of transients, all other parameters remained unchanged.

2.4. Data analysis

Data analyses were performed using MATLAB (R2020b, MathWorks, Natick, USA), including eddy-current correction (Klose, 1990) using the first acquired transient as a reference, zero-filling to yield an apparent spectral resolution of 0.24 Hz/point and Fourier transformation. The unsuppressed water peak in each transient of the pre- and post-fMRI PRESS spectra was modeled in the frequency domain using a Voigt lineshape function (Marshall et al., 1997) with a linear baseline to extract the water peak center frequency from each transient. Full-width half-maximum (FWHM) and the integral of the water signal were measured and reported to assess the change of lineshape. To compare frequency drift before and after fMRI, the mean absolute water peak frequency offset was calculated for each acquisition. Frequency offset was calculated as the difference between each transient's observed water signal frequency and the frequency of the first transient. The median drift is the median across the 95 datasets, of the mean offset throughout each measurement. Drift rate was measured pre-fMRI and over the same time period (5:20 min) of post-fMRI. The average drift rate is a mean across the 95 datasets which was calculated for each from the difference between the first and the last frequency offsets in Hz divided by the duration of the scan in minutes. Pearson's correlation coefficients (r) and two-sided paired t-tests were calculated between the mean absolute frequency offsets before and after fMRI for correlation and distribution analyses. Spearman's rank correlation coefficients (ρ) were measured for the correlation of operating hours and years of usage with frequency offsets. Differences on operating hours and years of usage among vendors were tested using Kruskal-Wallis test. A p-value less than 0.05 was considered statistically significant.

2.4.1. Repeated protocol

Sites were encouraged to repeat the acquisition protocol on a different day to investigate consistency and reproducibility of frequency drift characteristics. Pearson's correlation coefficients and intraclass correlation coefficients (ICC) were calculated for the mean absolute frequency offsets between the two runs. ICC calculation was based on a two-way mixed model using absolute agreement. The median values and interquartile ranges of the mean absolute frequency offsets across all datasets and within vendors are shown in violin plots with p-values from the paired t-tests. Datasets from the first and second day were plotted against each other to allow visualized observation for consistency between the two runs. All statistical analysis was performed using R (RStudio: Integrated Development for R. RStudio, PBC, Boston, MA) (R Core Team 2020).

2.5. Convolution of frequency drift and simulated spectra

To visualize the impact of the observed frequency drifts on a typical 5-min in vivo MRS protocol, a synthetic in vivo-like spectrum was generated using FID-A (Simpson et al., 2017) density-matrix simulations and the modeling results from a recent analysis of short-TE spectra in Osprey (Oeltzschner et al., 2020; Zollner et al., 2021), including weighted signals from 18 metabolites (TE = 35 ms; 2 kHz spectral width; 2048 complex samples; 2 Hz linewidth). The simulated spectrum was convolved with the frequency trace from the first 64 TRs of the phantom scan. The convolution involved Fourier transform and shifting the zero-frequency component to the center to replicate the simulated spectrum. Frequency shifts from the 64 pre-and post-fMRI PRESS transients were applied and re-averaged to obtain the final spectra. The simulated spectra with maximum and minimum drifts across all datasets were plotted to observe how extreme frequency drift affect signal intensities. The maximum amplitude of the 2.01 ppm NAA singlet was determined to compare the change of signal intensity of the synthetic ‘drift-affected’ spectra before and after fMRI. Additionally, the impact of linear drift (from 0 to 50 Hz range) was demonstrated for two scenarios. First, these synthetic drift time-courses were convolved into the same simulated short-TE spectrum, and the NAA peak height reported. Second, the offset dependence of GABA editing efficiency was simulated in FID-A using 15 ms editing pulses and TE 68 ms, and the change of relative GABA signal integral was reported as a function of linear drift.

3. Results

Of the data collected from 99 scanners, 4 were excluded from the final analysis due to unexpected artifacts or corruption of data that were unable to be processed. Thus, data from 95 scanners were ultimately analyzed. No data were excluded from the repeated scans. Table 1 summarizes the numbers of sites and datasets. Table 2 summarizes scanner details. The average estimated scanner operation time per day was 7.2 ± 2.9 hours (no differences across vendors: χ2 = 0.071; p = 0.965), and the average age of scanner was 5.5 ± 3.8 years (no differences across vendors: χ2 = 4.458; p = 0.108). Low correlations were observed between operating time (r = 0.17/0.13) and age of scanner (r = 0.026/0.19) with pre-/post-fMRI frequency drift respectively, all p > 0.05. The median (IQR) FWHM of the water signal was 2.43 (0.01) Hz (GE: 1.90 (0.02) Hz, Philips: 2.29 (0.03) Hz, Siemens: 2.78 (0.02) Hz) for pre-fMRI PRESS and 2.44 (0.02) Hz (GE:2.02 (0.03) Hz, Philips: 2.25 (0.03) Hz, Siemens: 2.76 (0.02) Hz) for post-fMRI. The median (IQR) integral was 0.03 (2.1E-5) (GE: 0.029 (3E-4), Philips: 0.033 (2E-4), Siemens: 0.025 (3E-4)) for pre-fMRI PRESS and 0.03 (9.5E-5) (GE: 0.025 (3E-4), Philips: 0.028 (2E-4), Siemens: 0.033 (1E-4)) for post-fMRI PRESS.

Table 2.

Scanner information for all datasets (n = 99).

Site ID Scanner model Software release Year of install Average hours of operation per day Gradient max. amplitude (mT/m) / slew rate (T/m/s) Mean absolute frequency offsets (Hz)
Pre-fMRI Post-fMRI (5:20 min) Post-fMRI (30:00 min)
G01a GE Discovery MR750 DV26 2010 12 50 / 200 0.30 0.16 1.66
G02a GE Discovery MR750 DV26 2019 1 50 / 200 0.14 0.19 1.66
G03a GE Discovery MR750 DV26 2014 9 50 / 200 0.05 0.16 1.47
G04a GE Discovery MR750 DV26 2010 11 50 / 200 0.08 0.68 2.46
G05a GE Discovery MR750 DV26 2009 8 50m/ 200 0.14 1.11 3.44
G06a GE Discovery MR750W DV25 2013 6 44 / 200 0.46 3.46 5.88
G07a GE Discovery MR750 DV26 2011 8 50 / 200 0.05 0.50 2.28
G08a GE SIGNA Premier RX27 2020 2 80 / 200 0.31 1.68 11.18
G09a GE SIGNA Premier RX27 2018 8 80 / 200 0.13 0.76 4.11
G10a GE SIGNA UHP 3T R27 2020 5 100 / 200 0.25 0.83 3.52
G11a GE SIGNA PET/MR MP26 2016 5 44 / 200 0.36 2.20 4.20
G12a GE Discovery MR750 DV25.1 2011 6 50 / 200 0.11 0.16 1.22
G15a GE Discovery MR750 DV26 2010 13 50 / 200 0.31 0.20 0.63
G16a GE Discovery MR750 DV26 2012 6 50 / 200 0.06 0.65 2.97
G17a GE Discovery MR750 DV25 2010 8 87 / 200 0.13 0.57 2.20
G18a GE SIGNA PET/MR MP26 2014 4 44 / 200 0.30 1.00 1.20
G19a GE Discovery MR750 DV26 2011 8 50 / 200 0.28 0.52 2.45
G20a GE Discovery MR750 DV26 2012 10 50 / 200 0.06 0.42 1.77
G21a# GE SIGNA Premier RX27 2019 10 80 / 200 n/a n/a n/a
G23a GE Discovery MR750 DV26 2016 5 50 / 200 0.04 0.50 2.56
G24a GE Discovery MR750 DV26 2012 6 50 / 200 0.14 0.54 2.34
G24b GE Discovery MR750 DV26 2013 6 50 / 200 0.06 1.04 3.75
P01a Philips Achieva R5.6.1 2018 6 40 / 200 1.80 1.77 3.17
P01b Philips Ingenia R5.6.1 2018 6 45 / 200 0.94 2.81 3.40
P02a Philips Achieva R5.3.1.3 2012 14 80 / 100 1.42 3.63 5.63
P02b Philips Ingenia R5.3.1.3 2015 8 45 / 200 0.65 1.75 2.70
P03a Philips Achieva R5.6.1 2018 4 40 / 120 0.64 7.19 8.28
P03b Philips Ingenia R5.6.1 2016 8 45 / 120 1.12 1.53 2.82
P04a Philips Achieva TX R5.6 2010 8 40 / 200 1.26 4.61 17.01
P05a Philips Achieva dStream R5.7.1 2009 9 80 / 200 2.67 5.91 15.72
P06a Philips Ingenia R5.4.1.1 2016 8 45 / 200 1.14 1.42 1.56
P06b Philips Achieva R5.3.1.2 2010 8 80 / 100 1.97 1.47 6.88
P06c Philips Ingenia Elition R5.6.1 2018 8 45 / 220 1.02 1.69 1.96
P07a Philips Ingenia R5.3.1.3 2017 6 80 / 200 0.13 0.45 4.96
P08a Philips ingenia Elition R5.6.1 2020 3 45 / 220 0.93 4.23 3.62
P09a Philips Ingenia R5.4.1 2019 7 n/a 1.50 1.00 4.09
P10a Philips Ingenia R5.4.1 2016 8 80 / 200 0.07 0.44 5.65
P11a Philips Achieva R5v30.02 2012 5 40 / 200 2.06 6.23 16.82
P12a Philips Ingenia R5.6.1 2019 5 45 / 220 0.87 0.09 5.66
P13a Philips Achieva dStream R5.6.1 2008 10 80 / 200 1.83 2.14 6.06
P15a Philips Ingenia Elition X R5.6.1 2019 6 45 / 220 0.74 0.74 4.63
P16a Philips Ingenia Elition X R5.6.1 2020 2 45 / 220 1.05 0.23 8.07
P17a Philips Ingenia CX R5.6.1 2019 2 40 / 200 1.40 0.63 1.67
P18a Philips Ingenia R5.6.1 2012 9 33 / 200 0.83 2.43 7.69
P18b Philips Ingenia R.5.61 2015 8 33 / 200 1.43 1.49 3.15
P18c Philips Ingenia Elition X R.5.61 2018 9 45 / 200 1.35 2.50 2.10
P19a Philips Achieva R5.4.1 2015 4 40 / 200 0.42 0.49 1.67
P20a Philips Achieva dStream R5.4.0.1 2013 10 40 / 200 3.46 4.49 13.86
P22a Philips Achieva dStream R5.7.1 2020 8 45 / 200 0.44 0.72 5.82
P23a Philips Achieva R5.4.1 2008 15 40 / 200 2.55 2.10 2.43
P24a Philips Achieva R5.6.1 2010 8 n/a 1.43 1.69 3.77
P25a Philips Achieva R3.3.2 2012 4 40 / 200 2.29 2.93 3.83
S01a Siemens Prisma VE11B 2016 4 80 / 200 0.07 0.21 0.49
S02a# Siemens Vida XA20 2020 12 60 / 200 n/a n/a n/a
S03a Siemens Prisma VE11C 2018 9 80 / 200 0.09 0.90 2.02
S03b Siemens Biograph mMR VE11P 2017 5 45 / 200 0.53 0.81 2.26
S03c Siemens Trio VB17 2006 4 45 / 200 0.04 0.60 0.87
S04a Siemens Skyra VE11C 2015 8 45 / 200 1.80 0.34 7.71
S05a Siemens Prisma VE11C 2018 4 80 / 200 0.03 0.05 0.56
S06a* Siemens Prisma VE11E 2019 8 40 / 200 0.03 0.22 0.93
S07a Siemens Biograph mMR VE11P 2019 8 45 / 200 0.46 0.41 2.71
S07b Siemens Prisma VE11E 2015 11 80 / 200 2.63 2.18 9.48
S08a Siemens Prisma VE11C 2016 5 80 / 200 0.02 0.02 0.35
S09a Siemens Verio VB17 2009 5 45 / 200 0.49 1.66 1.87
S10a Siemens Prisma VE11C 2020 3 80 / 200 0.02 0.02 0.34
S11a* Siemens Prisma VE11C 2017 6 80 / 200 0.09 0.09 0.74
S11c* Siemens Prisma VE11C 2015 3 80 / 200 0.09 0.11 0.22
S12a Siemens Skyra VE11E 2014 6 45 / 200 1.91 0.83 11.68
S13a* Siemens Prisma VE11C 2015 6 80 / 200 0.02 0.02 0.43
S13b* Siemens Prisma VE11C 2015 6 80 / 200 1.13 0.92 4.54
S13c*# Siemens Connectom VD13D 2015 6 300 / 200 n/a n/a n/a
S14a Siemens Skyra VD13A 2011 5 45 / 200 1.08 2.09 5.44
S15a Siemens Trio VB19a 2007 5 45 / 200 0.02 0.90 1.71
S15b Siemens Prisma VE11C 2002 10 80 / 200 0.11 1.49 3.90
S16a* Siemens Skyra VE11C 2012 9 45 / 200 0.47 1.65 3.23
S17a* Siemens Skyra VE11C 2019 3 45 / 200 0.19 0.38 4.74
S18a* Siemens Tim Trio VB17A 2009 8 45 / 200 0.03 0.14 0.21
S18b Siemens Skyra VE11C 2012 5 45 / 200 0.47 2.49 2.48
S19a* Siemens Prisma VE11C 2014 8 80 / 200 2.46 1.56 8.15
S20a Siemens Prisma VE11C 2018 3 80 / 200 2.13 1.49 7.50
S21a Siemens Prisma VE11C 2015 8 80 / 200 0.03 0.04 0.34
S22a* Siemens Prisma VE11C 2018 8 80 / 200 2.18 1.54 7.62
S22b*# Siemens Skyra VE11C 2020 12 45 / 200 n/a n/a n/a
S23a* Siemens Prisma VE11C 2016 8 80 / 200 1.66 1.24 5.70
S24a Siemens Prisma VE11C 2016 8 80 / 200 2.30 2.25 11.39
S25a Siemens Prisma VE11C 2016 8 80 / 200 0.04 0.10 0.13
S26a* Siemens Prisma VE11C 2016 8 80 / 200 0.41 0.44 2.25
S27a Siemens Prisma VE11C 2019 8 80 / 200 2.49 1.67 9.70
S27b Siemens Skyra VE11C 2019 8 45 / 200 0.19 1.00 6.54
S28a* Siemens Skyra E11-A 2015 17 45 / 200 1.03 0.70 5.59
S29a Siemens Prisma VE11E 2017 8 80 / 200 0.02 0.10 0.62
S30a Siemens Prisma VE11C 2018 9 80 / 200 0.06 0.26 0.82
S31a Siemens Prisma VE11c 2015 9 80 / 200 2.36 1.67 8.13
S33a* Siemens Prisma VE11C 2016 9 80 / 200 0.05 0.06 0.51
S37a Siemens Prisma VE11C 2016 3 80 / 200 0.08 0.64 0.33
S38a Siemens Prisma VE11C 2016 9 80 / 200 0.23 0.76 2.54
S40a* Siemens Prisma VE11C 2017 8 80 / 200 0.08 0.13 0.94
S40b* Siemens Prisma VE11C 2015 8 80 / 200 3.29 2.36 10.21
S99a Siemens Prisma VE11C 2019 7 80 / 200 1.00 0.96 4.32

indicates repeated protocol was performed.

indicates chiller/eco mode was off. If not specify, the setting was in default.

#

indicates data have been excluded due to noise artefact or headers unable to be read.

indicates reassigned site ID for P21a.

3.1. Frequency drift

Individual spectra from one of the highest-drifting scanners, before and after fMRI, are shown in Fig. 1a with frequency drift traces. The frequency drift traces are overlaid for all 95 initial scans in Fig. 1b. Scanners drifted by up to 7 Hz over 320 s before fMRI, and by up to 26 Hz within 30 min after 10 min of fMRI. Frequency drifts for the first 320 s before and after fMRI are shown in Fig. 1c. Violin plots of the mean absolute frequency offsets for all scanners are shown in Fig. 2a. Before fMRI, the median (IQR) was 0.44 (1.29) Hz. Mean drift across all scanners increased to 0.83 (1.29) Hz after fMRI for the first 5:20 min, and further increased to 3.15 (4.02) Hz for the full 30-min run. Average drift rates were 0.29 Hz/min and 0.43 Hz/min before and after fMRI, respectively. Due to the non-linear drift behavior of a few scanners, the drift rate was not determined across the full 30-min run. t-tests indicated that drift was significantly increased (t = -4.09, p < 0.05) after fMRI across all scanners. Correlation analysis indicated moderate correlation between drift across the first 64 transients before and after fMRI (r = 0.55, p < 0.05), as shown in Fig. 2b.

Fig. 1.

Fig 1

a) Individual transients pre- and post-fMRI PRESS (plotted in blue and red, respectively) from one of the highest drift datasets. The frequency offset derived from modeling the water signals is plotted (middle). Three hundred sixty averages correspond to 30 min total scan duration. Panel (b) shows water offset traces for all 95 scanners before and after fMRI for GE (green and light blue), Philips (orange and brown) and Siemens (blue and purple). Panel (c) shows the pre-fMRI PRESS traces and the same period (5:20 min) for post-fMRI traces.

Fig. 2.

Fig 2

a) Violin plots of mean absolute frequency offsets for all 95 scanners (median (solid line) and IQR (dashed line)); data from GE (green), Philips (orange) and Siemens (blue) are plotted. P-values show the mean values are significantly different before and after running the fMRI sequence. Panel (b) shows a scatterplot between pre-fMRI and early post-fMRI (first 5:20 min) with the confidence interval shaded in grey, in which a moderate correlation was observed.

3.2. Second acquisition from repeated protocol

Sixty scanners repeated the protocol on a different day. Frequency offsets recorded on two separate days before fMRI are correlated in Fig. 3a. The same plot is shown for post-fMRI data in Fig. 3b. Within these sixty scanners, the median (IQR) frequency drift before fMRI was 0.31 (1.09) Hz and 0.33 (1.14) Hz, for the first and repeated datasets, respectively. The mean absolute frequency offsets for each session were compared pairwise within-site for repeatability and correlation. ICC and Pearson's coefficients were 0.85 and 0.75, respectively, indicating good agreement and correlation between sessions for pre-fMRI datasets. Post-fMRI, median frequency drifts on the two days were 2.55 (3.06) Hz and 2.88 (2.98) Hz, with ICC and Pearson's coefficients being 0.95 and 0.90, respectively.

Fig. 3.

Fig 3

Frequency offsets from day 1 against day 2 a) before fMRI and b) after fMRI, for GE (green), Philips (orange) and Siemens (blue). Inserts show only those traces that remain within the gray box on the primary plot to allow for visualization of the lower-drift traces.

3.3. Intensity changes in simulated spectra between minimum and maximum drifts

Simulated spectra convolved with 64-transient water frequency drift traces (the highest and lowest drift case for each vendor before and after fMRI) are shown in Fig. 4. The intensity of the 2.01 ppm NAA singlet in the maximum-drift cases is reduced by 5%, 28% and 28% for GE, Philips and Siemens before fMRI, respectively, and by 26%, 44% and 18% after fMRI, respectively. The impact of linear drift (of up to 50 Hz range) on the NAA peak height is shown in Fig. 5a. Since drift does not impact noise levels, these peak signal losses represent predicted losses of SNR. The effective change in GABA editing efficiency seen with linear drift is shown in Fig. 5b. Note that this Fig. reports integral, which is unaffected by lineshape convolution, to isolate this aspect of drift.

Fig. 4.

Fig 4

Comparison of simulated spectra with frequency offsets applied between minimum and maximum drift for pre- and post-fMRI PRESS data. The minimum-drift case for each vendor (50% opacity) is overlaid with the maximum-drift case (opaque).

Fig. 5.

Fig 5

Impact of linear drift. Panel (a) shows the change in simulated NAA signal height as a function of the range of linear drift. Panel (b) shows the simulated GABA integral changes as a function of the same linear drift, due to editing efficiency losses.

3.4. Frequency drift in an approximately three-hour long acquisition

The frequency offsets for a single 171-min post-fMRI PRESS experiment (2048 transients) are shown in Fig. 6. Gradients and bore temperatures returned to their initial state within ~10 min. The mean absolute frequency offset was 13.9 (± 6.45) Hz and reached up to 21.5 Hz. The overall drift rate was 0.12 Hz/min but dropped to 0.03 Hz/min for the last 16 min (the last 196/2048 transients), suggesting the frequency drift approached equilibrium almost three hours after the EPI sequence. The site (G03a) provided this long acquisition data had amongst the lowest mean absolute drift in pre- and post-fMRI cases for the regular protocol, and a below average drift rate as shown in table 2.

Fig. 6.

Fig 6

Temperature change and water frequency offset before and after fMRI for the long PRESS acquisition. Panel (a) shows the corresponding gradient temperatures from sensors at different locations as well as the bore and scan room temperature. Panel (b) shows the change of frequency offsets after fMRI.

4. Discussion

This is a large multi-site study to date that has characterized the levels of B0 field drift in 3T MRI scanners. Results suggest that operating time and age of scanner have no significant correlations with frequency drift. Lineshapes of the acquired water signals are consistent in terms of their FWHM and integral.

4.1. Average frequency drift does not severely impact spectral data

The levels of B0 field instability that are tolerable vary between experiments, but for the majority of MRI and MRS methods, mean offsets below 1 Hz do not have any significant impact. Including the median-drift case observed in this study, spectra are virtually indistinguishable from minimum-drift spectra because this level of instability is small compared to the typical in vivo linewidth. Moreover, the line-broadening effect seen on less stable scanners can readily be addressed using retrospective frequency correction recommended in recent consensus on MRS data processing (Near et al., 2020; Wilson et al., 2019). This is necessary even for extremely stable scanners, since it also addresses frequency and phase instability arising from subject motion.

Although the drift is significantly greater after fMRI, it typically remains in the same order of magnitude. The previous observation of field drift associated with a single run of fMRI (Harris et al., 2014), over 1 Hz/min, is above average, although falling within the range of results seen here. For a majority of scanners, although a single fMRI run does result in a less stable scanner, the extent of that impact is moderate, and the benefits of performing fMRI early in multimodal imaging protocols (particularly task-related fMRI to identify functional regions for MRS assessment) probably outweigh the detriment to MRS. However, it is important to consider that the heating effects of imaging sequences are additive, and although a single 10-min fMRI scan has limited effects, MRS performed after several runs of such scans or other EPI-based sequence such as DWI (Lange JMRI 2011) might be more seriously impacted. Furthermore, the variation among sites suggests testing drift on a specific scanner is worthwhile prior to establishing a protocol.

4.1.1. Cooling and frequency drift

While gradient cooling systems return gradient temperatures to equilibrium relatively rapidly, they do not fully prevent the dissipation of energy to elsewhere within the scanner. Cooling of other scanner parts, manifested as field drift, may require a much longer time to be stabilized. Therefore, in addition to considering the implications for sequence ordering within a protocol, one must also consider what the scanner was doing in the previous imaging session(s). For this reason, it has been suggested that running MRS scans ‘from cold’ will result in the greatest scanner stability especially before running B0 field sensitive sequences. Any system feature that alters the gradient temperature during downtime (e.g., overnight to reduce energy consumption) may make pre-fMRI scans less stable than at typical daytime equilibrium; an equilibration period immediately after startup is recommended for such scanners.

4.2. Frequency drift is largely consistent and reproducible within individual scanners

Over the duration of typical experiments (~10 min), the drift observed is relatively linear. Some scanners do show smooth changes of drift rate, e.g., appearing to reach a heating/cooling equilibrium and returning towards the initial center frequency. Philips scanners also illustrate some behavior that is not smooth, presumably reflecting automatic changes in an external cooling system. This dip appears between 10 and 20 min after fMRI in about two-thirds of Philips scanners. Although the extent of the dips varies, it does not seem to be related to the model or the age of the scanners. Types of cooling systems may be of interest for further study. The patterns of drift seen are also relatively reproducible (ICC » 0.9), and even smooth non-linearities in behavior are mostly reproduced in repeat measurements. This suggests that maintaining consistent scan order within protocols will reduce the variance in drift observed. This is common practice in studies, but particularly where acquiring the full protocol is in doubt, e.g., in studies of low-compliance groups, randomization of scan order is sometimes implemented. Change of SNR has been demonstrated using simulated in vivo spectra convolved with frequency traces. Results suggest that the relative change of NAA and GABA signals are minimal within 1 Hz as of lower than the median drift in a typical 5-min MRS.

4.3. Limitations

One disadvantage of the data visualizations in Fig. 1, Fig. 2, Fig. 3 is that they over-emphasize the outlier sites with large drift and tend to conceal the sites displaying very little drift. Frequency drift induced by gradient heating is a known issue, however, readings from sensors for gradient temperature monitoring have not been widely reported, while the number and locations of them also vary across vendors. Temperature readings are archived in log files, which can be retrieved retrospectively after the scan. However, the files consist of a lot of other information for the scan that make temperature retrieval more complicated. Furthermore, gradient temperatures are stored in time series and users would have to match the time of the scan with the data in log files. Real-time gradient temperature monitoring would be helpful, but it is not an available option for all scanners. Passive shim elements play a key role in heat dissipation. However, the number and bulk weight of passive shim installed are poorly reported as many of the sites that participated in this study found the information inaccessible. Finally, other studies have reported phantom temperature could be increased by approximately 1–1.5°C during a 30-min turbo spin-echo sequence (Graedel et al., 2015) and approximately 1°C during a one-hour long steady-state free precession sequence (El-Sharkawy et al., 2006). Although phantom temperature variation might have slight influence on water frequency that would, to first order, be common across all vendors, phantom heating induced by absorption of the RF energy is neglected. Human body temperature should be largely consistent throughout the scan and the effects of heating from RF is minimal.

4.4. Conclusion

While previous studies have established that scanner drift occurs, and that it can have a negative impact on the quality of data acquired (Evans et al., 2013; Harris et al., 2014; Rowland et al., 2017; Tsai et al., 2016),these studies have been carried out on a single scanner. It has not been clear to what extent these issues are generalizable to all MR scanners, or whether such issues have become over-emphasized. Overall, the results of this study are encouraging. Median levels of drift are low for cold scanners, and moderate to severe drift only appears after EPI in a small number of scanners. The implications of instability in the main magnetic field are very different for different imaging and spectroscopy sequences. It is helpful to consider the quantitative results of this study in the context of these effects. Real-time field-frequency lock for MRS acquisition is suggested to avoid drift related data instability especially after multiple long EPI acquisitions including fMRI and DTI when field drift is much more pronounced and for multi-center collaborations in which data are obtained from different scanners. In conclusion, this study measured field drift before and after 10 min of fMRI/EPI on 95 3T scanners using the MRS water signal.

CRediT authorship contribution statement

Steve C.N. Hui: Conceptualization, Methodology, Formal analysis, Writing – original draft, Writing – review & editing, Visualization, Project administration. Mark Mikkelsen: Methodology, Software, Writing – review & editing. Helge J. Zöllner: Methodology, Software, Writing – review & editing. Vishwadeep Ahluwalia: Validation, Resources, Writing – review & editing. Sarael Alcauter: Validation, Resources, Writing – review & editing. Laima Baltusis: Validation, Resources, Writing – review & editing. Deborah A. Barany: Validation, Resources, Writing – review & editing. Laura R. Barlow: Validation, Resources, Writing – review & editing. Robert Becker: Validation, Resources, Writing – review & editing. Jeffrey I. Berman: Validation, Resources, Writing – review & editing. Adam Berrington: Validation, Resources, Writing – review & editing. Pallab K. Bhattacharyya: Validation, Resources, Writing – review & editing. Jakob Udby Blicher: Validation, Resources, Writing – review & editing. Wolfgang Bogner: Validation, Resources, Writing – review & editing. Mark S. Brown: Validation, Resources, Writing – review & editing. Vince D. Calhoun: Validation, Resources, Writing – review & editing. Ryan Castillo: Validation, Resources, Writing – review & editing. Kim M. Cecil: Validation, Resources, Writing – review & editing. Yeo Bi Choi: Validation, Resources, Writing – review & editing. Winnie C.W. Chu: Validation, Resources, Writing – review & editing. William T. Clarke: Validation, Resources, Writing – review & editing. Alexander R. Craven: Validation, Resources, Writing – review & editing. Koen Cuypers: Validation, Resources, Writing – review & editing. Michael Dacko: Validation, Resources, Writing – review & editing. Camilo de la Fuente-Sandoval: Validation, Resources, Writing – review & editing. Patricia Desmond: Validation, Resources, Writing – review & editing. Aleksandra Domagalik: Validation, Resources, Writing – review & editing. Julien Dumont: Validation, Resources, Writing – review & editing. Niall W. Duncan: Validation, Resources, Writing – review & editing. Ulrike Dydak: Validation, Resources, Writing – review & editing. Katherine Dyke: Validation, Resources, Writing – review & editing. David A. Edmondson: Validation, Resources, Writing – review & editing. Gabriele Ende: Validation, Resources, Writing – review & editing. Lars Ersland: Validation, Resources, Writing – review & editing. C. John Evans: Validation, Resources, Writing – review & editing. Alan S.R. Fermin: Validation, Resources, Writing – review & editing. Antonio Ferretti: Validation, Resources, Writing – review & editing. Ariane Fillmer: Validation, Resources, Writing – review & editing. Tao Gong: Validation, Resources, Writing – review & editing. Ian Greenhouse: Validation, Resources, Writing – review & editing. James T. Grist: Validation, Resources, Writing – review & editing. Meng Gu: Validation, Resources, Writing – review & editing. Ashley D. Harris: Validation, Resources, Writing – review & editing. Katarzyna Hat: Validation, Resources, Writing – review & editing. Stefanie Heba: Validation, Resources, Writing – review & editing. Eva Heckova: Validation, Resources, Writing – review & editing. John P. Hegarty: Validation, Resources, Writing – review & editing. Kirstin-Friederike Heise: Validation, Resources, Writing – review & editing. Shiori Honda: Validation, Resources, Writing – review & editing. Aaron Jacobson: Validation, Resources, Writing – review & editing. Jacobus F.A. Jansen: Validation, Resources, Writing – review & editing. Christopher W. Jenkins: Validation, Resources, Writing – review & editing. Stephen J. Johnston: Validation, Resources, Writing – review & editing. Christoph Juchem: Validation, Resources, Writing – review & editing. Alayar Kangarlu: Validation, Resources, Writing – review & editing. Adam B. Kerr: Validation, Resources, Writing – review & editing. Karl Landheer: Validation, Resources, Writing – review & editing. Thomas Lange: Validation, Resources, Writing – review & editing. Phil Lee: Validation, Resources, Writing – review & editing. Swati Rane Levendovszky: Validation, Resources, Writing – review & editing. Catherine Limperopoulos: Validation, Resources, Writing – review & editing. Feng Liu: Validation, Resources, Writing – review & editing. William Lloyd: Validation, Resources, Writing – review & editing. David J. Lythgoe: Validation, Resources, Writing – review & editing. Maro G. Machizawa: Validation, Resources, Writing – review & editing. Erin L. MacMillan: . Richard J. Maddock: . Andrei V. Manzhurtsev: Validation, Resources, Writing – review & editing. María L. Martinez-Gudino: Validation, Resources, Writing – review & editing. Jack J. Miller: Validation, Resources, Writing – review & editing. Heline Mirzakhanian: Validation, Resources, Writing – review & editing. Marta Moreno-Ortega: Validation, Resources, Writing – review & editing. Paul G. Mullins: Validation, Resources, Writing – review & editing. Shinichiro Nakajima: Validation, Resources, Writing – review & editing. Jamie Near: Validation, Resources, Writing – review & editing. Ralph Noeske: Validation, Resources, Writing – review & editing. Wibeke Nordhøy: Validation, Resources, Writing – review & editing. Georg Oeltzschner: Validation, Resources, Writing – review & editing. Raul Osorio-Duran: Validation, Resources, Writing – review & editing. Maria C.G. Otaduy: Validation, Resources, Writing – review & editing. Erick H. Pasaye: Validation, Resources, Writing – review & editing. Ronald Peeters: Validation, Resources, Writing – review & editing. Scott J. Peltier: Validation, Resources, Writing – review & editing. Ulrich Pilatus: Validation, Resources, Writing – review & editing. Nenad Polomac: Validation, Resources, Writing – review & editing. Eric C. Porges: Validation, Resources, Writing – review & editing. Subechhya Pradhan: Validation, Resources, Writing – review & editing. James Joseph Prisciandaro: Validation, Resources, Writing – review & editing. Nicolaas A Puts: Validation, Resources, Writing – review & editing. Caroline D. Rae: Validation, Resources, Writing – review & editing. Francisco Reyes-Madrigal: Validation, Resources, Writing – review & editing. Timothy P.L. Roberts: Validation, Resources, Writing – review & editing. Caroline E. Robertson: Validation, Resources, Writing – review & editing. Jens T. Rosenberg: Validation, Resources, Writing – review & editing. Diana-Georgiana Rotaru: Validation, Resources, Writing – review & editing. Ruth L O'Gorman Tuura: Validation, Resources, Writing – review & editing. Muhammad G. Saleh: Validation, Resources, Writing – review & editing. Kristian Sandberg: Validation, Resources, Writing – review & editing. Ryan Sangill: Validation, Resources, Writing – review & editing. Keith Schembri: Validation, Resources, Writing – review & editing. Anouk Schrantee: Validation, Resources, Writing – review & editing. Natalia A. Semenova: Validation, Resources, Writing – review & editing. Debra Singel: Validation, Resources, Writing – review & editing. Rouslan Sitnikov: Validation, Resources, Writing – review & editing. Jolinda Smith: Validation, Resources, Writing – review & editing. Yulu Song: Validation, Resources, Writing – review & editing. Craig Stark: Validation, Resources, Writing – review & editing. Diederick Stoffers: Validation, Resources, Writing – review & editing. Stephan P. Swinnen: Validation, Resources, Writing – review & editing. Rongwen Tain: Validation, Resources, Writing – review & editing. Costin Tanase: Validation, Resources, Writing – review & editing. Sofie Tapper: Validation, Resources, Writing – review & editing. Martin Tegenthoff: Validation, Resources, Writing – review & editing. Thomas Thiel: Validation, Resources, Writing – review & editing. Marc Thioux: Validation, Resources, Writing – review & editing. Peter Truong: Validation, Resources, Writing – review & editing. Pim van Dijk: Validation, Resources, Writing – review & editing. Nolan Vella: Validation, Resources, Writing – review & editing. Rishma Vidyasagar: Validation, Resources, Writing – review & editing. Andrej Vovk: Validation, Resources, Writing – review & editing. Guangbin Wang: Validation, Resources, Writing – review & editing. Lars T. Westlye: Validation, Resources, Writing – review & editing. Timothy K. Wilbur: Validation, Resources, Writing – review & editing. William R. Willoughby: Validation, Resources, Writing – review & editing. Martin Wilson: Validation, Resources, Writing – review & editing. Hans-Jörg Wittsack: Validation, Resources, Writing – review & editing. Adam J. Woods: Validation, Resources, Writing – review & editing. Yen-Chien Wu: Validation, Resources, Writing – review & editing. Junqian Xu: Validation, Resources, Writing – review & editing. Maria Yanez Lopez: Validation, Resources, Writing – review & editing. David K.W. Yeung: Validation, Resources, Writing – review & editing. Qun Zhao: Validation, Resources, Writing – review & editing. Xiaopeng Zhou: Validation, Resources, Writing – review & editing. Gasper Zupan: Validation, Resources, Writing – review & editing. Richard A.E. Edden: Conceptualization, Methodology, Validation, Writing – review & editing, Supervision, Funding acquisition.

Declaration of Competing Interest

Jack J. Miller would like to acknowledge the support of a Novo Nordisk Research Fellowship run in conjunction with the University of Oxford. Francisco Reyes-Madrigal has served as a speaker for Janssen (Johnson & Johnson) and AstraZeneca. Marc Thioux and Pim van Dijk were supported by The Netherlands Organization for Health Research and Development (ZonMW) and the Dorhout Mees Foundation. All other authors have no conflict of interest to declare.

Acknowledgments

Acknowledgements

This work was supported by NIH grants R01 EB016089, R01 EB023963, R21 AG060245, S10 OD021726, K01 AA025306, K99 AG062230, K99 DA051315, K99 EB028828, R01 MH110270, R01-DC008871, S10 OD012336, S10 OD021648, P41 EB031771, Taiwan MOST grant 108-2410-H-038-008-MY2, JST COI grant JPMJCE1311, ERC grant #249516, DLR 01ZX1909A SySMedSUDs, Natural Sciences and Engineering Research Council of Canada RGPIN/03875-2017, CONACYT grant CF-2019-6390, The European Research Council under the European Union's Horizon 2020 Research and Innovation program (ERC StG 802998), Ariane Fillmer has received funding from the 18HLT09 NeuroMET2 project within the EMPIR programme co-financed by the Participating States and from the European Union's Horizon 2020 research and innovation programme. The contribution of Kristian Sandberg and Katarzyna Hat to this article is based upon work from COST Action CA18106, supported by COST (European Cooperation in Science and Technology). Marc Thioux and Pim van Dijk received funding from ZonMW, Dorhout Mees Foundation, Heinsius Houbolt Foundation and the European Union's Horizon 2020 research and innovation programme under the Marie Skłodowska-Curie grant agreement No 764604. NeuRA Imaging, part of the Australian National Imaging Facility, is supported by the National Collaborative Research Infrastructure Scheme. We would also like to thank Dr. Yoshihiro Noda from Keio University for his assistant on data collection.

Data and code availability statements

All data were collected prospectively using MRI phantom. They will be available on the NITRC portal in the “Big Drift” project repository (https://www.nitrc.org/projects/bigdrift/). See appendix in manuscript for more details. Data analysis was performed using MATLAB (R2020b, MathWorks, Natick, USA), and statistical analysis using R (RStudio: Integrated Development for R. RStudio, PBC, Boston, MA). All functions and packages are freely available on MATHWORKS and GITHUB.

Appendix

A subset of the data presented in this work has been made available on the NITRC portal in the “Big Drift” project repository (https://www.nitrc.org/projects/bigdrift/) for benchmark and further analyses. It is distributed freely under the Creative Commons Attribution-NonCommercial-ShareAlike license. Community members are encouraged to make use of this resource for developing and optimizing frequency drift related methods.

References

  1. R Core Team . R Foundation for Statistical Computing; Vienna, Austria: 2020. R: A Language and Environment for Statistical Computing. [Google Scholar]
  2. Ebel A., Maudsley A.A. Detection and correction of frequency instabilities for volumetric 1H echo-planar spectroscopic imaging. Magn. Reson. Med. 2005;53:465–469. doi: 10.1002/mrm.20367. [DOI] [PubMed] [Google Scholar]
  3. Edden R.A., Barker P.B. Spatial effects in the detection of gamma-aminobutyric acid: improved sensitivity at high fields using inner volume saturation. Magn. Reson. Med. 2007;58:1276–1282. doi: 10.1002/mrm.21383. [DOI] [PubMed] [Google Scholar]
  4. Edden R.A., Oeltzschner G., Harris A.D., Puts N.A., Chan K.L., Boer V.O., Schar M., Barker P.B. Prospective frequency correction for macromolecule-suppressed GABA editing at 3T. J. Magn. Reson. Imaging. 2016;44:1474–1482. doi: 10.1002/jmri.25304. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Edden R.A., Puts N.A., Barker P.B. Macromolecule-suppressed GABA-edited magnetic resonance spectroscopy at 3T. Magn. Reson. Med. 2012;68:657–661. doi: 10.1002/mrm.24391. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. El-Sharkawy A.M., Schar M., Bottomley P.A., Atalar E. Monitoring and correcting spatio-temporal variations of the MR scanner's static magnetic field. MAGMA. 2006;19:223–236. doi: 10.1007/s10334-006-0050-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Ernst T., Li J. A novel phase and frequency navigator for proton magnetic resonance spectroscopy using water-suppression cycling. Magn. Reson. Med. 2011;65:13–17. doi: 10.1002/mrm.22582. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Evans C.J., Puts N.A., Robson S.E., Boy F., McGonigle D.J., Sumner P., Singh K.D., Edden R.A. Subtraction artifacts and frequency (mis-)alignment in J-difference GABA editing. J. Magn. Reson. Imaging. 2013;38:970–975. doi: 10.1002/jmri.23923. [DOI] [PubMed] [Google Scholar]
  9. Foerster B.U., Tomasi D., Caparelli E.C. Magnetic field shift due to mechanical vibration in functional magnetic resonance imaging. Magn. Reson. Med. 2005;54:1261–1267. doi: 10.1002/mrm.20695. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Graedel N.N., Polimeni J.R., Guerin B., Gagoski B., Bonmassar G., Wald L.L. An anatomically realistic temperature phantom for radiofrequency heating measurements. Magn. Reson. Med. 2015;73:442–450. doi: 10.1002/mrm.25123. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Harris A.D., Glaubitz B., Near J., John Evans C., Puts N.A., Schmidt-Wilcke T., Tegenthoff M., Barker P.B., Edden R.A. Impact of frequency drift on gamma-aminobutyric acid-edited MR spectroscopy. Magn. Reson. Med. 2014;72:941–948. doi: 10.1002/mrm.25009. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Helms G., Piringer A. Restoration of motion-related signal loss and line-shape deterioration of proton MR spectra using the residual water as intrinsic reference. Magn. Reson. Med. 2001;46:395–400. doi: 10.1002/mrm.1203. [DOI] [PubMed] [Google Scholar]
  13. Henry P.G., van de Moortele P.F., Giacomini E., Nauerth A., Bloch G. Field-frequency locked in vivo proton MRS on a whole-body spectrometer. Magn. Reson. Med. 1999;42:636–642. doi: 10.1002/(sici)1522-2594(199910)42:4<636::aid-mrm4>3.0.co;2-i. [DOI] [PubMed] [Google Scholar]
  14. Keating B., Ernst T. Real-time dynamic frequency and shim correction for single-voxel magnetic resonance spectroscopy. Magn. Reson. Med. 2012;68:1339–1345. doi: 10.1002/mrm.24129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Klose U. In vivo proton spectroscopy in presence of eddy currents. Magn. Reson. Med. 1990;14:26–30. doi: 10.1002/mrm.1910140104. [DOI] [PubMed] [Google Scholar]
  16. Lange T., Zaitsev M., Buechert M. Correction of frequency drifts induced by gradient heating in 1H spectra using interleaved reference spectroscopy. J. Magn. Reson. Imaging. 2011;33:748–754. doi: 10.1002/jmri.22471. [DOI] [PubMed] [Google Scholar]
  17. Lee C.Y., Choi I.Y., Lee P. Prospective frequency correction using outer volume suppression-localized navigator for MR spectroscopy and spectroscopic imaging. Magn. Reson. Med. 2018;80:2366–2373. doi: 10.1002/mrm.27340. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Marshall I., Higinbotham J., Bruce S., Freise A. Use of Voigt lineshape for quantification of in vivo 1H spectra. Magn. Reson. Med. 1997;37:651–657. doi: 10.1002/mrm.1910370504. [DOI] [PubMed] [Google Scholar]
  19. Mikkelsen M., Barker P.B., Bhattacharyya P.K., Brix M.K., Buur P.F., Cecil K.M., Chan K.L., Chen D.Y., Craven A.R., Cuypers K., Dacko M., Duncan N.W., Dydak U., Edmondson D.A., Ende G., Ersland L., Gao F., Greenhouse I., Harris A.D., He N., Heba S., Hoggard N., Hsu T.W., Jansen J.F.A., Kangarlu A., Lange T., Lebel R.M., Li Y., Lin C.E., Liou J.K., Lirng J.F., Liu F., Ma R., Maes C., Moreno-Ortega M., Murray S.O., Noah S., Noeske R., Noseworthy M.D., Oeltzschner G., Prisciandaro J.J., Puts N.A.J., Roberts T.P.L., Sack M., Sailasuta N., Saleh M.G., Schallmo M.P., Simard N., Swinnen S.P., Tegenthoff M., Truong P., Wang G., Wilkinson I.D., Wittsack H.J., Xu H., Yan F., Zhang C., Zipunnikov V., Zollner H.J., Edden R.A.E. Big GABA: Edited MR spectroscopy at 24 research sites. Neuroimage. 2017;159:32–45. doi: 10.1016/j.neuroimage.2017.07.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Mikkelsen M., Rimbault D.L., Barker P.B., Bhattacharyya P.K., Brix M.K., Buur P.F., Cecil K.M., Chan K.L., Chen D.Y., Craven A.R., Cuypers K., Dacko M., Duncan N.W., Dydak U., Edmondson D.A., Ende G., Ersland L., Forbes M.A., Gao F., Greenhouse I., Harris A.D., He N., Heba S., Hoggard N., Hsu T.W., Jansen J.F.A., Kangarlu A., Lange T., Lebel R.M., Li Y., Lin C.E., Liou J.K., Lirng J.F., Liu F., Long J.R., Ma R., Maes C., Moreno-Ortega M., Murray S.O., Noah S., Noeske R., Noseworthy M.D., Oeltzschner G., Porges E.C., Prisciandaro J.J., Puts N.A.J., Roberts T.P.L., Sack M., Sailasuta N., Saleh M.G., Schallmo M.P., Simard N., Stoffers D., Swinnen S.P., Tegenthoff M., Truong P., Wang G., Wilkinson I.D., Wittsack H.J., Woods A.J., Xu H., Yan F., Zhang C., Zipunnikov V., Zollner H.J., Edden R.A.E. Big GABA II: Water-referenced edited MR spectroscopy at 25 research sites. Neuroimage. 2019;191:537–548. doi: 10.1016/j.neuroimage.2019.02.059. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Mullins P.G., McGonigle D.J., O'Gorman R.L., Puts N.A., Vidyasagar R., Evans C.J., Cardiff Symposium on, M.R.S.o.G. Edden R.A. Current practice in the use of MEGA-PRESS spectroscopy for the detection of GABA. Neuroimage. 2014;86:43–52. doi: 10.1016/j.neuroimage.2012.12.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Near J., Edden R., Evans C.J., Paquin R., Harris A., Jezzard P. Frequency and phase drift correction of magnetic resonance spectroscopy data by spectral registration in the time domain. Magn. Reson. Med. 2015;73:44–50. doi: 10.1002/mrm.25094. [DOI] [PMC free article] [PubMed] [Google Scholar]
  23. Near J., Harris A.D., Juchem C., Kreis R., Marjanska M., Oz G., Slotboom J., Wilson M., Gasparovic C. Preprocessing, analysis and quantification in single-voxel magnetic resonance spectroscopy: experts' consensus recommendations. NMR Biomed. 2020:e4257. doi: 10.1002/nbm.4257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Oeltzschner G., Zollner H.J., Hui S.C.N., Mikkelsen M., Saleh M.G., Tapper S., Edden R.A.E. Osprey: Open-source processing, reconstruction & estimation of magnetic resonance spectroscopy data. J. Neurosci. Methods. 2020;343 doi: 10.1016/j.jneumeth.2020.108827. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Poblador Rodriguez E., Moser P., Dymerska B., Robinson S., Schmitt B., van der Kouwe A., Gruber S., Trattnig S., Bogner W. A comparison of static and dynamic B0 mapping methods for correction of CEST MRI in the presence of temporal B0 field variations. Magn. Reson. Med. 2019;82:633–646. doi: 10.1002/mrm.27750. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Rowland B.C., Liao H., Adan F., Mariano L., Irvine J., Lin A.P. Correcting for Frequency Drift in Clinical Brain MR Spectroscopy. J. Neuroimaging. 2017;27:23–28. doi: 10.1111/jon.12388. [DOI] [PubMed] [Google Scholar]
  27. Simpson R., Devenyi G.A., Jezzard P., Hennessy T.J., Near J. Advanced processing and simulation of MRS data using the FID appliance (FID-A)-An open source, MATLAB-based toolkit. Magn. Reson. Med. 2017;77:23–33. doi: 10.1002/mrm.26091. [DOI] [PubMed] [Google Scholar]
  28. Tal A., Gonen O. Localization errors in MR spectroscopic imaging due to the drift of the main magnetic field and their correction. Magn. Reson. Med. 2013;70:895–904. doi: 10.1002/mrm.24536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Thiel T., Czisch M., Elbel G.K., Hennig J. Phase coherent averaging in magnetic resonance spectroscopy using interleaved navigator scans: compensation of motion artifacts and magnetic field instabilities. Magn. Reson. Med. 2002;47:1077–1082. doi: 10.1002/mrm.10174. [DOI] [PubMed] [Google Scholar]
  30. Tsai S.Y., Fang C.H., Wu T.Y., Lin Y.R. Effects of Frequency Drift on the Quantification of Gamma-Aminobutyric Acid Using MEGA-PRESS. Sci. Rep. 2016;6:24564. doi: 10.1038/srep24564. [DOI] [PMC free article] [PubMed] [Google Scholar]
  31. van der Veen J.W., Marenco S., Berman K.F., Shen J. Retrospective correction of frequency drift in spectral editing: The GABA editing example. NMR Biomed. 2017;30 doi: 10.1002/nbm.3725. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Waddell K.W., Avison M.J., Joers J.M., Gore J.C. A practical guide to robust detection of GABA in human brain by J-difference spectroscopy at 3 T using a standard volume coil. Magn. Reson. Imaging. 2007;25:1032–1038. doi: 10.1016/j.mri.2006.11.026. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Weiner M.W., Veitch D.P., Aisen P.S., Beckett L.A., Cairns N.J., Green R.C., Harvey D., Jack C.R., Jr., Jagust W., Morris J.C., Petersen R.C., Salazar J., Saykin A.J., Shaw L.M., Toga A.W., Trojanowski J.Q., Alzheimer's Disease Neuroimaging, I. The Alzheimer's Disease Neuroimaging Initiative 3: Continued innovation for clinical trial improvement. Alzheimers Dement. 2017;13:561–571. doi: 10.1016/j.jalz.2016.10.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Wilson M. Robust retrospective frequency and phase correction for single-voxel MR spectroscopy. Magn. Reson. Med. 2019;81:2878–2886. doi: 10.1002/mrm.27605. [DOI] [PubMed] [Google Scholar]
  35. Wilson M., Andronesi O., Barker P.B., Bartha R., Bizzi A., Bolan P.J., Brindle K.M., Choi I.Y., Cudalbu C., Dydak U., Emir U.E., Gonzalez R.G., Gruber S., Gruetter R., Gupta R.K., Heerschap A., Henning A., Hetherington H.P., Huppi P.S., Hurd R.E., Kantarci K., Kauppinen R.A., Klomp D.W.J., Kreis R., Kruiskamp M.J., Leach M.O., Lin A.P., Luijten P.R., Marjanska M., Maudsley A.A., Meyerhoff D.J., Mountford C.E., Mullins P.G., Murdoch J.B., Nelson S.J., Noeske R., Oz G., Pan J.W., Peet A.C., Poptani H., Posse S., Ratai E.M., Salibi N., Scheenen T.W.J., Smith I.C.P., Soher B.J., Tkac I., Vigneron D.B., Howe F.A. Methodological consensus on clinical proton MRS of the brain: Review and recommendations. Magn. Reson. Med. 2019;82:527–550. doi: 10.1002/mrm.27742. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Zollner H.J., Povazan M., Hui S.C.N., Tapper S., Edden R.A.E., Oeltzschner G. Comparison of different linear-combination modeling algorithms for short-TE proton spectra. NMR Biomed. 2021;34:e4482. doi: 10.1002/nbm.4482. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

All data were collected prospectively using MRI phantom. They will be available on the NITRC portal in the “Big Drift” project repository (https://www.nitrc.org/projects/bigdrift/). See appendix in manuscript for more details. Data analysis was performed using MATLAB (R2020b, MathWorks, Natick, USA), and statistical analysis using R (RStudio: Integrated Development for R. RStudio, PBC, Boston, MA). All functions and packages are freely available on MATHWORKS and GITHUB.

RESOURCES