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Objective: Individuals with Autism Spectrum Disorder (ASD) or Early-Onset Psychosis (EOP) both experience substantial difficulties with social cognition (Spek et al. 2012; Lanillos et al. 2020); however, the impact of therapy and medication use on their social cognition has not yet been examined (Lai et al. 2014; Schiffman et al. 2018). This project will explore the effects of the history of therapy and medication use as moderating variables between neural architecture and social cognition performance. Participants and Methods: T1-weighted imaging data were acquired on a 3T Siemens scanner for 51 ASD and EOP participants (Mean Age = 16.33), with 41 individuals endorsing history of therapy and 23 endorsing history of medication use across groups. Cortical thickness was calculated using FreeSurfer imaging analysis software (v5.3; Fischel et al., 2002) for social brain regions including inferior parietal lobe (IPL), middle temporal lobe (MPL), caudal anterior cingulate cortex (cACC), rostral anterior cingulate cortex (rACC), fusiform gyrus, precuneus cortex, and insular cortex. The Awareness of Social Inference Test (TASIT; McDonald et al., 2006) was administered to assess social cognition performance. After controlling for individuals that had a history of both therapy and medication use, Pearson's correlations were utilized to examine the relationship between cortical thickness and social cognition performance in ASD and EOP patients. The PROCESS Procedure moderation analysis in SPSS was utilized to determine if history of therapy or medication use moderated the relationship between cortical thickness and social cognition performance (Hayes, 2018). Results: Across groups, there was a negative association between an individual's cACC thickness and TASIT Do score (r = -.415, p =.005) as well as the total TASIT score (r = -.325, p =.031). Additionally, there was a positive association between an individual's precuneus cortical thickness and their TASIT Say score (r =.440, p =.003). Results of the moderation analyses revealed that lack of medication use was associated with greater rACC thickness and higher TASIT Say score (R 2 Change =.1281 mm, p =.0191). Additionally, lack of past therapy experience was associated with greater insular thickness and higher TASIT Think scores (R2 Change =.1957 mm, p =.0033). Conversely, past therapy history was associated with greater fusiform gyrus thickness and higher TASIT Say score (R2 Change =.1115 mm, p =.0262). Conclusions: Our results suggest that for individuals without a history of therapy or medication use, higher cortical thickness of the rACC and insula support better social cognition performance; whereas for individuals with past therapy experience, higher cortical thickness of the fusiform cortex underlies better social cognition performance. Collectively, these findings suggest that an individual's history of therapy or medication use may be relevant variables to consider when examining the relationship between neural cortical thickness and social cognition performance in these neuropsychiatric conditions. [ABSTRACT FROM AUTHOR]

Objective: Previous research has found that trauma is a risk factor for developing early-onset psychosis (EOP), both exhibiting widespread structural abnormalities and social cognitive dysfunction (Hoy et al., 2012; Nair et al., 2020; Rotiker et al., 2018). However, few studies have investigated the association between trauma, neural architecture, and social behaviors. The current study examines whether trauma exposure moderates the association between cortical volume and thickness and social cognition in EOP. Participants and Methods: T1-weighted whole-brain magnetic resonance data were acquired on a 3T Siemens scanner for 23 adolescents with EOP aged 12-21 years (M = 16.12), and 20 age-matched controls (M = 17.22). Cortical volume and thickness were calculated using the Freesurfer software suite (v5.3; Reuter et al., 2012). Based on prior research, bilateral structures of interest included the rostral anterior cingulate cortex (rACC), insula, precuneus, and superior frontal cortex. Social measures included the WebCNP Emotion Recognition (KER40) and Emotion Differentiation Test (MED36) accuracy score (Gur et al., 2010), The Awareness of Social Inference Test Total Score (TASIT; McDonald et al., 2003), and Social Responsiveness Scale, 2nd Edition (SRS-2; Constantino & Gruber, 2012). Trauma exposure was assessed using the Structured Clinical Interview Diagnostic (controls n = 5; EOP n = 9; First et al., 2015). Pearson's correlations and independent t-tests were used to examine the relationship between cortical measurements and social cognition. Additionally, PROCESS macro (Hayes, 2018) was used to examine if trauma history statistically moderated the relationship between cortical measurements and social cognition performance. Results: Significant group differences in SRS-2 scores were observed, as EOP participants scored 24.272 points higher than controls (t = 20.724, p <.001). Across both groups, there was a negative correlation between the SRS-2 score and precuneus volume (r = -.438, p =.011) and thickness (r = -.383, p =.028), TASIT total and superior frontal volume (r = -.349, p =.023), and KER40 and insular volume (r = -.437, p =.20). Further, the moderation analysis revealed that the relationships between precuneus volume and SRS-2 scores, precuneus thickness and MED36 scores, and rACC thickness and KER40 scores depended on experiencing trauma across both groups. Participants with trauma across groups had increased precuneus volume associated with higher SRS-2 scores (p =.0442). Experiencing trauma was also associated with lower precuneus cortical thickness and lower MED36 scores (p =.0172). Conversely, lack of trauma experience was associated with greater rACC thickness and higher KER40 scores (p =.0119). Conclusions: Our findings indicate that past traumatic experiences may be a moderating factor in the relationship between atypical volume and thickness of social brain regions and social cognition. Overall, the significant interactions between trauma exposure and increased volume and thickness in both EOP and control participants were associated with increased impairment on social cognition measures. These findings emphasize the importance of accounting for the impact of early life adversities on brain development and how it may be relevant to social impairments, especially in individuals experiencing psychosis. [ABSTRACT FROM AUTHOR]