“…Upon stabilization at each temperature, shimming was conducted to correct for temperature‐related susceptibility changes, 26,32 followed by a proton Point‐RESolved Spectroscopy (PRESS) sequence with the following parameters: TE = 40 ms, TR = 2500 ms, flip angle = 90°, averages = 150, voxel size = 3 × 3 × 3 mm 3 , acquisition bandwidth = 6010 Hz, and acquisition time = 375 s. Proton MR spectroscopic thermometry was used because it noninvasively measures temperature based on frequency differences between temperature‐dependent water and temperature‐independent metabolites. The three frequencies of the N ‐acetyl‐aspartate (NAA), creatine (Cr), and choline (Ch) singlets at 2.01, 3.03, and 3.19 ppm were assumed to be temperature independent and fixed, and were used as references to improve the reproducibility of the temperature measurement 58 . Upon completion of the acquisitions, the data were exported to TopSpin 4.2 software (Bruker), where the frequency difference between water and the metabolites was reconstructed and the average temperature was computed according to 58 where , and are the frequencies of the water, Cr, Ch, and NAA peaks, respectively, in units of ppm.…”