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. Author manuscript; available in PMC: 2010 Apr 19.
Published in final edited form as: Alcohol Clin Exp Res. 2008 Jul;32(7):1113–1123. doi: 10.1111/j.1530-0277.2008.00692.x

Table 3.

Greater Areas of Activity in DRD4.L Group Compared With the Control Group

Region BA Peak Z-score TLRC
DRD4.L > Controls
Prepriming
 L OFC* 47 3.17 −42, 43, −5
 L subcallosal gyrus 25 3.10 −10, 19, −15
 L IFG 47 2.92 −36, 29, −15
 R putamen 2.79 24, 11, −7
 L OFC* 47 2.54 −14, 23, −15
 R insula 13 2.41 28, 17, −7
 R OFC 11 2.26 40, 45, −13
 R OFC 11 2.21 12, 25, −15
 R VTA/midbrain 1.90 10, −17, −15
Postpriming
 None
Controls > DRD4.L
Prepriming
 R medial frontal gyrus 10 3.65 20, 43, −1
 L ACG 32 3.38 16, 33, 7
 R caudate 3.05 22, 21, 5
 R ACG 32 2.90 16, 41, −1
 L caudate 2.66 −18, 27, 1
 R IFG 11 1.78 26, 31, −25
Postpriming
 R IFG 47 3.93 23, 31, −11
 L OFC 11 3.64 −24, 35, −13
 L caudate 3.58 22 27 −7
 R globus pallidus 3.57 20, −13, −5
 L thalamus 3.35 −10, −3, −13
 R VTA/midbrain 3.30 14, −9, −9
 R putamen 3.21 −10, 5, −9
 R ACG 32 2.99 18, 33, −11
 L VTA/midbrain 2.87 −6, −19, −9
 L putamen 2.80 −24, 9, −7
 R thalamus 2.70 18, −5, 13

L, left; R, right; OFC, orbitofrontal cortex; IFG, inferior frontal gyrus; VTA, ventral tegmental area; ACG, anterior cingulate gyrus.

Without priming, the DRD4.L subjects had greater BOLD response in all of the ROIs compared to the controls (p < 0.05). None of these structures was greater in the DRD4.L subjects after priming. Maximum loci of activation are listed for each substrate as anatomical labels, Brodmann area (BA) corresponding peak z-score, and Talairach (TLRC) co-ordinates corresponding of greater BOLD response in the risk allele group compared with the nonrisk allele group.

*

Foci of peak activation (i.e., L OFC) that overlap with OPRM1.G individuals.