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. Author manuscript; available in PMC: 2017 Feb 2.
Published in final edited form as: Am J Med Genet B Neuropsychiatr Genet. 2013 Mar 8;162B(3):245–252. doi: 10.1002/ajmg.b.32141

Table 2.

Study variables by child COMT genotype.

Variable Child COMT val158met Genotype
Study 1 (Stony Brook University)a Study 2 (Western University)b
val/val (N = 73) val/met + met/met (N =340) val/val (N = 102) val/met + met/met (N =260)
M (SD) M (SD) M (SD) M (SD)
Anxiety 11.09 (7.23)* 9.19 (8.39)* 9.66 (2.18) 9.02 (1.92)
Depression 5.12 (4.19)** 3.89 (4.37)** 13.21 (0.70)* 12.65 (1.52)*
ODD 5.36 (7.83) 4.81 (6.74) 13.44 (3.24) 12.99 (3.12)
ADHD 2.60 (6.19) 2.75 (6.50) 36.70 (9.22) 35.79 (8.01)

p < 0.10,

*

p < .05,

**

p < .01.

1

Mean ranks were tested using Wilcoxon rank sum test, as symptom scores were not normally distributed due to absence of internalizing symptoms in some children. These children received a score of ‘0’ on the relevant symptom sub-scale on the PAPA.

a

Symptom data based on maternal interview reports from the PAPA.

b

Primary caregiver reports from the ECI-4.

Note: N, sample size; SD, standard deviation; PPVT, Peabody Picture Vocabulary Test; SES, socioeconomic status as indexed by Hollingshead’s Four Factor Index of Social Status [Hollingshead, 1975]; PAPA, Preschool Age Psychiatric Assessment; ECI-4, Early Childhood Inventory-4 [Gadow and Sprafkin, 1997]; COMT, Catechol-O-methyltransferase; val, valine; met, methionine.