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. 2018 Aug 8;44(2):390–398. doi: 10.1038/s41386-018-0174-x

Table 2.

Brain regions showing dose-related effects of ondansetron

BA k x y z pcorr r r lower r upper
Insula (middle, posterior) (L) 13 1409 −38 −10 4 0.02 0.57 0.35 0.73
Superior temporal (L) 22, 41, 42 −38 −36 8 0.04
Precentral/inferior frontal/postcentral (L) 2, 6, 9, 43, 44 −54 6 26 0.03
Insula (middle, posterior) (R) 13 1165 36 −36 10 0.02 0.55 0.33 0.71
Superior/middle temporal (R) 22, 38, 41, 42 60 −16 10 0.03
Postcentral/precentral (R) 2, 3, 4, 6 595 58 −8 36 0.03 0.56 0.33 0.71
Anterior cingulate (B) 33 158 −6 6 30 0.04 0.52 0.29 0.69
Middle frontal (L) 9 36 −36 36 32 0.05 0.46 0.22 0.65
Supplementary motor area (R) 6 19 12 2 58 0.05 0.51 0.27 0.68
Supplementary motor area (L) 6 17 −6 2 48 0.05 0.44 0.19 0.63
Insula (posterior)/superior temporal 13 16 −46 −36 18 0.05 0.44 0.19 0.63

Data are whole-brain corrected at a family-wise error rate of p < 0.05 using threshold-free cluster enhancement and nonparametric permutation analysis. Positive correlation coefficients reflect greater reductions (i.e., decreased activity) for OND (compared to PL) as dosage increases

BA Brodmann’s areas, k cluster extent, pcorr whole-brain-corrected p value, R right, L left, B bilateral, r Pearson’s correlation coefficient with 95% confidence interval bounds, coordinates are in MNI space