Abstract:Magnetic resonance spectroscopy (MRS) enables the noninvasive quantification of up to 20 neurochemicals in selected brain regions and has found many applications in the study of the cerebellum in health and disease. The neurochemicals accessible by MRS include neuronal and glial markers, neurotransmitters, markers of cellular energetics, and antioxidants and, therefore, provide means to assess neuronal dysfunction/loss, glial activation, energy metabolism, and oxidative stress. As a result, the methodology has… Show more
“…This study demonstrates that nearly identical neurochemical profiles consisting of 13–17 metabolites are obtained in two different brain regions in relatively large healthy cohorts by different operators at two MR sites. The acquisition of high‐quality MRS data from the cerebellum and brainstem is particularly challenging due to their caudal location in the head and broader intrinsic linewidths relative to other cerebral VOI . We were able to obtain high‐quality MRS data in a dual‐site setting due the consistency of obtaining artifact‐free short T E spectra using an in‐house developed and highly optimized pulse sequence and identical B 0 and B 1 adjustment protocols.…”
Section: Discussionmentioning
confidence: 99%
“…A previously described semi‐LASER sequence was used to achieve lower apparent T 2 relaxation, minimal J ‐coupling evolution, and smaller chemical shift displacement errors relative to the standard PRESS sequence. Two relatively challenging brain regions were chosen for this two‐site comparison: the cerebellar vermis and pons .…”
Purpose
To determine if neurochemical concentrations obtained at two MRI sites using clinical 3 T scanners can be pooled when a highly optimized, non-vendor short-echo, single voxel proton MRS pulse sequence is utilized in conjunction with identical calibration and quantification procedures.
Methods
A modified semi-LASER sequence (TE = 28 ms) was used to acquire spectra from two brain regions (cerebellar vermis and pons) on two Siemens 3 T scanners using the same B0 and B1 calibration protocols from two different cohorts of healthy volunteers (N=24–33 per site) matched for age and BMI. Spectra were quantified with LCModel using water scaling.
Results
The spectral quality was very consistent between the two sites and allowed reliable quantification of at least 13 metabolites in the vermis and pons compared to 3 – 5 metabolites in prior multi-site MRS trials using vendor-provided sequences. The neurochemical profiles were nearly identical at the two sites and showed the feasibility to detect inter-individual differences in the healthy brain.
Conclusion
Highly reproducible neurochemical profiles can be obtained on different clinical 3 T scanners at different sites, provided that the same, optimized acquisition and analysis techniques are utilized. This will allow pooling of multi-site data in clinical studies, which is particularly critical for rare neurological diseases.
“…This study demonstrates that nearly identical neurochemical profiles consisting of 13–17 metabolites are obtained in two different brain regions in relatively large healthy cohorts by different operators at two MR sites. The acquisition of high‐quality MRS data from the cerebellum and brainstem is particularly challenging due to their caudal location in the head and broader intrinsic linewidths relative to other cerebral VOI . We were able to obtain high‐quality MRS data in a dual‐site setting due the consistency of obtaining artifact‐free short T E spectra using an in‐house developed and highly optimized pulse sequence and identical B 0 and B 1 adjustment protocols.…”
Section: Discussionmentioning
confidence: 99%
“…A previously described semi‐LASER sequence was used to achieve lower apparent T 2 relaxation, minimal J ‐coupling evolution, and smaller chemical shift displacement errors relative to the standard PRESS sequence. Two relatively challenging brain regions were chosen for this two‐site comparison: the cerebellar vermis and pons .…”
Purpose
To determine if neurochemical concentrations obtained at two MRI sites using clinical 3 T scanners can be pooled when a highly optimized, non-vendor short-echo, single voxel proton MRS pulse sequence is utilized in conjunction with identical calibration and quantification procedures.
Methods
A modified semi-LASER sequence (TE = 28 ms) was used to acquire spectra from two brain regions (cerebellar vermis and pons) on two Siemens 3 T scanners using the same B0 and B1 calibration protocols from two different cohorts of healthy volunteers (N=24–33 per site) matched for age and BMI. Spectra were quantified with LCModel using water scaling.
Results
The spectral quality was very consistent between the two sites and allowed reliable quantification of at least 13 metabolites in the vermis and pons compared to 3 – 5 metabolites in prior multi-site MRS trials using vendor-provided sequences. The neurochemical profiles were nearly identical at the two sites and showed the feasibility to detect inter-individual differences in the healthy brain.
Conclusion
Highly reproducible neurochemical profiles can be obtained on different clinical 3 T scanners at different sites, provided that the same, optimized acquisition and analysis techniques are utilized. This will allow pooling of multi-site data in clinical studies, which is particularly critical for rare neurological diseases.
“…). Of note, the cerebellum presents challenges for MRS, such as broader intrinsic line widths than other brain regions (Öz ), however, its anatomical landmarks present an advantage for consistent placement of the VOI within and between animals. Thus, the mean test‐retest coefficient of variation using the same methodology in the mouse cerebellum is ≤ 5% for six of the reported metabolites, including tCr, tCho and Tau, and ≤ 10% for five reported metabolites, including Gln (Öz et al .…”
Section: Discussionmentioning
confidence: 99%
“…Interestingly, glucose and glycogen (the main storage form of glucose in the brain) levels in the cerebellum are higher than other brain regions (Swanson et al . ) and, together with high creatine kinase activity and tCr levels, the cerebellum appears to be distinct from other brain regions in its energy buffering capacity (Öz ).…”
Spinocerebellar ataxia type 1 (SCA1) is a hereditary, progressive and fatal movement disorder that primarily affects the cerebellum. Non-invasive imaging markers to detect early disease in SCA1 will facilitate testing and implementation of potential therapies. We have previously demonstrated the sensitivity of neurochemical levels measured by 1H magnetic resonance spectroscopy (MRS) to progressive neurodegeneration using a transgenic mouse model of SCA1. In order to investigate very early neurochemical changes related to neurodegeneration, here we utilized a knock-in mouse model, the Sca1154Q/2Q line, which displays milder cerebellar pathology than the transgenic model. We measured cerebellar neurochemical profiles of Sca1154Q/2Q mice and wild-type littermates using 9.4T MRS at ages 6, 12, 24, and 39 weeks and assessed the cerebellar pathology of a subset of the mice at each time point. The Sca1154Q/2Q mice displayed very mild cerebellar pathology even at 39 weeks, however, were distinguished from wild types by MRS starting at 6 weeks. Taurine and total choline levels were significantly lower at all ages and glutamine and total creatine levels were higher starting at 12 weeks in Sca1154Q/2Q mice than controls, demonstrating the sensitivity of neurochemical levels to neurodegeneration related changes in the absence of overt pathology.
“…We used coils that were capable of achieving sufficient B 1 for spectroscopy (with minimal chemical shift displacement) in deep brain regions at both fields. We focused on two brain regions that are of interest for neurological diseases and that present different levels of technical challenges for MRS: the posterior cingulate, a key node in the default mode network , which is affected in a number of neurological and psychiatric disorders , and the cerebellum, which is affected in multiple movement disorders and is technically more challenging for study by MRS (due to its caudal location in the brain and broader intrinsic linewidths than most other cortical areas).…”
Purpose
To determine the test-retest reproducibility of neurochemical concentrations obtained with a highly optimized, short-echo, single voxel proton MRS pulse sequence at 3T and 7T using state-of-the-art hardware.
Methods
A semi-LASER sequence (TE = 26–28ms) was used to acquire spectra from the posterior cingulate and cerebellum at 3T and 7T from 6 healthy volunteers who were scanned weekly 4 times on both scanners. Spectra were quantified with LCModel.
Results
More neurochemicals were quantified with mean Cramér-Rao lower bounds (CRLB) ≤ 20% at 7T than at 3T despite comparable frequency-domain SNR. While CRLB were lower at 7T (p < 0.05), between-session coefficients of variance (CVs) were comparable at the two fields with 64 transients. Five metabolites were quantified with between-session CVs ≤ 5% at both fields. Analysis of subspectra showed that a minimum achievable CV was reached with a lower number of transients at 7T for multiple metabolites and that between-session CVs were lower at 7T than at 3T with fewer than 64 transients.
Conclusion
State-of-the-art MRS methodology allows excellent reproducibility for many metabolites with 5 minute data averaging on clinical 3T hardware. Sensitivity and resolution advantages at 7T are important for weakly represented metabolites, short acquisitions and small volumes-of-interest.
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