Sec. Brain Imaging and Stimulation
Corrigendum: Repeatability and Reproducibility of in-vivo Brain Temperature Measurements
- 1Department of Psychology, University of Alabama at Birmingham (UAB), Birmingham, AL, United States
- 2Department of Neurobiology, University of Alabama at Birmingham (UAB), Birmingham, AL, United States
- 3University of Alabama at Birmingham Epilepsy Center (UABEC), Birmingham, AL, United States
- 4Department of Neurology, University of Alabama at Birmingham (UAB), Birmingham, AL, United States
- 5Department of Radiology, Miller School of Medicine, University of Miami, Miami, FL, United States
- 6Department of Neurosurgery, University of Alabama at Birmingham (UAB), Birmingham, AL, United States
by Sharma, A. A., Nenert, R., Mueller, C., Maudsley, A. A., Younger, J. W., and Szaflarski, J. P. (2020). Front. Hum. Neurosci. 14:598435. doi: 10.3389/fnhum.2020.598435
In the original article, there was a mistake in Figure 1 as published.
The original figure was adapted from Dehkharghani et al. (2015), but this adaptation was not appropriately described and referenced in the manuscript. We apologize for this oversight. The figure has been revised: the adapted portion has been replaced with a new graphic and the caption now appropriately indicates that a portion was adapted from a previously published article. The corrected Figure 1 appears below.
Figure 1. Brain temperature can be non-invasively derived from volumetric magnetic resonance spectroscopic imaging (MRSI) data by calculating the frequency difference between the temperature-sensitive water peak and one or more metabolite peaks that are temperature-insensitive (left*). When using creatine as the reference, voxel-level brain temperature can be calculated according to the following equation: TCRE = −102.61(ΔH20−CRE) + 206.1°C, ΔH20−CRE = chemical shift difference between the creatine and water resonances. Example TCRE calculations are provided for a participant's single tissue slice (right). Representative spectra illustrate ΔH20−CRE derivations, with plots depicting a water-suppressed metabolite spectrum (red line), with an overlay that indicates the location of the reference water signal (blue line). Spectral plots were created within the Metabolite Imaging and Data Analysis System (MIDAS) software package, and the figure was created using BioRender. *Adapted from Dehkharghani et al. (2015).
The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
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Dehkharghani, S., Mao, H., Howell, L., Zhang, X., Pate, K. S., Magrath, P. R., et al. (2015). Proton resonance frequency chemical shift thermometry: experimental design and validation toward high-resolution noninvasive temperature monitoring and in vivo experience in a non-human primate model of acute ischemic stroke. Am. J. Neuroradiol. 36, 1128–1135. doi: 10.3174/ajnr.A4241
Keywords: MRS, brain temperature, MR thermometry, neuroinflammation, neuroimaging
Citation: Sharma AA, Nenert R, Mueller C, Maudsley AA, Younger JW and Szaflarski JP (2021) Corrigendum: Repeatability and Reproducibility of in-vivo Brain Temperature Measurements. Front. Hum. Neurosci. 15:780797. doi: 10.3389/fnhum.2021.780797
Received: 21 September 2021; Accepted: 04 November 2021;
Published: 26 November 2021.
Edited and reviewed by: Dajiang Zhu, University of Texas at Arlington, United States
Copyright © 2021 Sharma, Nenert, Mueller, Maudsley, Younger and Szaflarski. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ayushe A. Sharma, firstname.lastname@example.org