Table 3.
Genotype | N | BPD score ± STD | F | df | p | η2 | power | |
---|---|---|---|---|---|---|---|---|
COMT | Met/Met | 34 | 4.79 ± 2.54 | 0.367 | 2,131 | 0.694 | 0.006 | 0.108 |
Met/Val | 70 | 4.71 ± 2.29 | ||||||
Val/Val | 32 | 5.16 ± 2.57 | ||||||
DAT1 | 9/9 | 11 | 4.64 ± 2.87 | 0.120 | 2,131 | 0.887 | 0.002 | 0.068 |
40 bp | 9/10 | 48 | 4.75 ± 2.74 | 0.082 | 1,132 | 0.775 | 0.001 | 0.059 |
VNTR | 10/10* | 77 | 4.92 ± 2.13 | |||||
DRD2 | B1/B1 | 3 | 3.33 ± 3.22 | 1.712 | 2,131 | 0.184 | 0.025 | 0.355 |
TaqIB | B1/B2 | 37 | 5.38 ± 2.31 | 1.518 | 1,132 | 0.220 | 0.011 | 0.231 |
B2/B2 | 96 | 4.68 ± 2.40 | ||||||
TaqID | C/C | 27 | 4.30 ± 2.54 | 1.490 | 2,131 | 0.229 | 0.022 | 0.313 |
C/T | 59 | 5.31 ± 2.28 | ||||||
T/T | 50 | 4.58 ± 2.43 | ||||||
TaqIA | A1/A1 | 4 | 3.75 ± 2.75 | 0.460 | 2,131 | 0.632 | 0.007 | 0.124 |
A1/A2 | 41 | 4.90 ± 2.56 | 0.001 | 1,132 | 0.970 | 0 | 0.050 | |
A2/A2 | 91 | 4.86 ± 2.34 | ||||||
DRD4 | 1/1 | 4 | 3.25 ± 2.06 | 1.611 | 2,131 | 0.204 | 0.024 | 0.336 |
120 bp | 1/2 | 40 | 5.18 ± 2.18 | 1.604 | 1,132 | 0.208 | 0.012 | 0.242 |
dup | 2/2 | 92 | 4.76 ± 2.50 | |||||
-616 | C/C | 44 | 5.48 ± 2.45 | 5.146 | 2,131 | 0.007 | 0.073 | 0.818 |
C/G | 56 | 4.80 ± 2.36 | 8.152 | 1,132 | 0.005 | 0.058 | 0.809 | |
G/G | 36 | 4.11 ± 2.27 | ||||||
-521 | C/C | 34 | 5.00 ± 2.54 | 0.463 | 2,131 | 0.630 | 0.007 | 0.124 |
C/T | 65 | 4.62 ± 2.38 | 0.354 | 1,132 | 0.553 | 0.003 | 0.091 | |
T/T | 37 | 5.08 ± 2.37 | ||||||
48 bp | 7/7 | 3 | 5.67 ± 1.53 | 0.282 | 2,131 | 0.754 | 0.004 | 0.094 |
VNTR | one 7 | 35 | 4.77 ± 2.38 | 0.134 | 1,132 | 0.715 | 0.001 | 0.065 |
no 7 | 98 | 4.84 ± 2.45 | ||||||
Haplotype | 0 | 68 | 4.40 ± 2.34 | 3.602 | 2,131 | 0.030 | 0.052 | 0.658 |
-616 C ~ | 1 | 50 | 5.14 ± 2.46 | 6.969 | 1,132 | 0.009 | 0.050 | 0.746 |
-521 T | 2 | 18 | 5.67 ± 2.30 |
The mean ± SD of the sum of borderline symptoms (BPD score) from the self-report SCID-II Screen questionnaire are presented for the different genotype groups. Where it is indicated, in the second set of univariate ANOVAs rare homozygote genotypes (n < 5) or literature-based genotypes were grouped together with the heterozygotes for the fixed factor; sex and age were used as covariates.
* At the DAT1 VNTR one 10/11 and one 10/12 sample were grouped together with the 10/10 (9-allele absent) genotype group.