Table 1.
CON | SCH | SCH low | SCHhigh | |
Onset | ||||
μV | ||||
Fz | 0.40** | -1.30 | -0.68 | -1.98 |
1.41 | 1.68 | 1.42 | 1.77 | |
Cz | 1.13** | -0.37 | 0.32 | -1.14 |
1.35 | 1.14 | 1.91 | 2.24 | |
Pz | 0.62 | -0.12 | 0.88* | -1.25 |
1.50 | 2.13 | 1.26 | 2.41 | |
Fp1 | -0.32* | -1.27 | -0.59 | -2.03 |
1.30 | 1.28 | 0.81 | 1.31 | |
Fp2 | -0.35* | -1.37 | -0.59* | -2.24 |
1.30 | 1.44 | 0.87 | 1.49 | |
C3' | 0.33 | -0.17 | 0.33 | -0.74 |
0.90 | 1.68 | 1.32 | 1.94 | |
C4' | 0.57 | -0.01 | 0.46 | -0.53 |
0.99 | 1.29 | 1.21 | 1.25 | |
Peak | ||||
μV | ||||
Fz | 1.31** | -0.06 | 0.85* | -1.08 |
1.64 | 1.71 | 0.91 | 1.87 | |
Cz | 1.90* | 0.44 | 1.21 | -0.42 |
1.64 | 1.58 | 1.95 | 2.56 | |
Pz | 0.65 | -0.30 | 0.56* | -1.28 |
1.31 | 1.71 | 1.19 | 2.29 | |
Fp1 | 0.13 | -0.41 | 0.58** | -1.52 |
1.26 | 1.58 | 1.04 | 1.35 | |
Fp2 | 0.20 | -0.40 | 0.77** | -1.71 |
1.38 | 1.82 | 1.27 | 1.43 | |
C3' | 0.76 | 0.11 | 0.44 | -0.26 |
1.04 | 1.26 | 1.17 | 1.34 | |
C4' | 0.95 | 0.22 | 0.76 | -0.39 |
0.82 | 1.59 | 1.26 | 1.78 | |
Other Group Variables | ||||
St. P50rat | 0.40 | 0.35 | 0.35 | 0.35 |
0.30 | 0.22 | 0.21 | 0.25 | |
S1Epochs | 98** | 77 | 83 | 71 |
12 | 23 | 18 | 28 | |
S2Epochs | 101** | 85 | 94 | 76 |
12 | 23 | 16 | 26 | |
Tobacco | 34 | 75 | 108 | 38 |
47 | 73 | 66 | 63 |
Mean amplitudes in μV (standard deviation). *) p < 0.05; **) p < 0.01 (post-hoc pairwise comparisons, Bonferroni corrected) when in (CON) denoting probability of significant difference between healthy controls (CON, N = 24) and all the schizophrenia spectrum patients (SCH, N = 17), when in (SCHlow) denoting probability of significant difference between patients having a negative symptom score (sum of five global SANS (not including global attention) items) ranging 0–7 (SCHlow, N = 9) and the patients having scores ranging 8–12 (SCHhigh, N = 8). The P50 ratio (S2/S1 amplitude) following traditional 10–50 Hz digital filtering has previously been reported [5], where it is compared to two other types of digital filtering. Number of included sweeps in the EP in both stimuli (S1 and S2) differs between healthy comparisons subjects and patients, but not within the patient sample.