Skip to main content
. 2018 Oct 24;19(1):99. doi: 10.1186/s10194-018-0924-5

Table 2.

Effect of tDCS on trigeminal nociceptive processing

MNI
X Y Z
Anatomical area kE T pFWE
cluster
pFWE
peak
−22 8–16 L Amygdalaa 107 4.48 .005 .001
−12 2 4 L Basal gangliaa 208 4.24 .033 .006
26 0–20 R Amygdalaa 125 4.18 .002 .001
56–30 -8 R Mid. temporal gyrus 74 4.17 NA NA
−10 -28 70 L M1 and premotor cortexa 162 4.11 .010 .012
−14 -10 18 L Thalamusa 39 3.99 .015 .008
56–18 6 R Superior temporal gyrus 86 3.97 NA NA
14 4 6 R Basal gangliaa 94 3.93 .027 .029
−50 -32 12 L Superior temporal gyrus 49 3.85 NA NA
66–8 18 R Postcentral gyrusa 24 3.81 .042 .025
−40 -2 -18 L Posterior Insular cortex 27 3.77 NS NS
−6 -4 44 L Cingulate cortexa 47 3.77 .03 .027
10–24 74 R Suppl. motor/premotor cortex 25 3.73 NS NS
4 14 0 R Basal ganglia / Caudate ncl.a 59 3.68 .027 .032
38 2 54 R DLPFCa 44 3.67 .044 .047
44 42 4 R DLPFC 42 3.58 NS NS

Areas with significant DC-stimulation induced alterations (postcathodal vs. postanodal). Illustration in Fig. 2. Exploratory significance level punc < .0005. Additional region of interest analysis (ROI) with applied Family-Wise-Error correction for the neuropain-matrix as indicated in the materials and method section (apFWE < 0.05)

R = right, L = left, BL = bilateral, Ke = cluster extend, MNI = Montreal Neurological Institute: NA = not applicable, NS = not significant. M1 = primary motorcortex, DLPFC = dorsolateral prefrontal cortex