Table 2.
Main Effects of Subject Group, Stimulus Type and Hemisphere.
Main Effects of Subject Group: | |||
---|---|---|---|
Component | F(1,38) | p value | Driven By |
P400 Latency | 4.16 | 0.048 | Faster responses in High-Risk than Low-Risk infants1 |
Nc Amplitude | 4.69 | 0.037 | Larger negative responses in Low-Risk than High-Risk infants2 |
Main Effects of Stimulus Type: | |||
---|---|---|---|
Component | F(1,38) | p value | Driven By |
N290 Latency | 8.63 | 0.006 | Faster responses to Objects than Faces1 |
N290 Amplitude | 5.12 | 0.030 | Larger negative responses to Faces than Objects3 |
P400 Amplitude | 6.69 | 0.014 | Larger positive responses to Objects than Faces4 |
Nc Amplitude | 8.69 | 0.005 | Larger negative responses to Objects than Faces5 |
Main Effects of Hemisphere: | |||
---|---|---|---|
Component | F(1,38) | p value | Driven By |
P100 Amplitude | 5.27 | 0.027 | Larger positive responses in Left than Right hemisphere6 |
N290 Amplitude | 8.32 | 0.006 | Larger negative responses in Right than Left hemisphere6 |
P400 Amplitude | 7.57 | 0.009 | Larger positive responses in Left than Right hemisphere6 |
The interpretation of this main effect is modified by the subject group × stimulus type interaction, see Results.
This effect, which does not interact with stimulus type, indicates that Low-Risk infants may have allocated more overall attention than High-Risk infants.
This result mirrors that seen in previous ERP studies of typical infants (30).
This result, although somewhat surprising, is similar to the non-face advantage for the P400 previously reported in ERP studies of typical infants (30).
The Nc is generally believed to be tied to salience/attention (which is thought to differ between familiar and unfamiliar stimuli), not face vs. object processing per se (see 33). However, note that the current study did not find familiarity effects for the Nc (in either Low- or High-Risk infants), which could be because our familiar vs. unfamiliar stimuli did not differ sufficiently in salience (see 33 for discussion). Also, note that the current study found no interactions between familiarity and subject group, which is not consistent with results from previous neural imaging studies that reported differences in the response to familiar vs. unfamiliar faces between individuals with ASD and typical controls (ERPs: 81, fMRI: 99). Again, the null finding of the current study could result if our familiar vs. unfamiliar stimuli did not differ sufficiently in salience. Other reasons for a discrepancy between the current and previous studies include different ages (infants vs. children) and different diagnostic categories (High-Risk infants vs. individuals diagnosed with ASD) across studies.
The interpretation of this main effect is modified by the subject group × hemisphere interaction, see Results.