ePoster

ALTERED PAIN PROCESSING AND CORTICO–STRIATAL–THALAMIC CIRCUITRY IN CHILDREN WITH EARLY-ONSET PSYCHOSIS

Hanne van der Heijdenand 15 co-authors

Boston Children's Hospital Harvard Medical School

FENS Forum 2026 (2026)
Barcelona, Spain
Board PS07-10AM-568

Presentation

Date TBA

Board: PS07-10AM-568

Poster preview

ALTERED PAIN PROCESSING AND CORTICO–STRIATAL–THALAMIC CIRCUITRY IN CHILDREN WITH EARLY-ONSET PSYCHOSIS poster preview

Event Information

Poster Board

PS07-10AM-568

Abstract

Aims

: Pain and somatosensory aversions are understudied features of early-onset psychosis (EOP). We aimed to identify clinical and neurobehavioral correlates of abnormal pain and somatosensory experiences in children with EOP.
Methods: Clinical assessments and child- (male or female; ages 12-18 years)/parent-reported outcomes were administered to children with EOP (N=31) and compared to chronic pain (CP, N=29), attention-deficit/hyperactivity disorder (ADHD, N=30), and healthy controls (HCs, N=20). Children with EOP and HCs were additionally phenotyped using quantitative sensory testing (QST), cognitive tasks, and structural and functional magnetic resonance imaging (MRI). The EOP cohort also completed a questionnaire battery at 6-months follow-up.
Results: Children with EOP showed more severe pain and somatosensory aversions than those with ADHD or HCs, but less than CP patients, with reports stable at follow-up. Thermal sensitivities on QST were associated with negative symptom severity (ρ=0.49, p=0.009) and self-reported cognitive difficulties (ρ=-0.37, p=0.009). Using fMRI, EOP patients exhibited increased evoked pain responses in the striatum (p<0.05) (Figure 1A) and higher cortico-striatal-thalamic connectivity (p<0.001) (Figure 1B), while striatal connectivity patterns reflective of dopamine transporter density (Figure 1C), were linked to negative symptoms (ρ=-0.42, p=0.05) and pain-related parameters (ρ=0.65, p=0.001). Reduced striatal and paracentral volumes were observed (p<0.05), with nucleus accumbens volumes inversely associated with pain episode frequency (ρ=-0.49, p=0.02).
Conclusions: Pain and somatosensory disturbances in EOP are associated with disruptions in cortico–striatal–thalamic circuits. Upon further validation, clinical and neurobehavioral markers that can detect dysregulated pain behaviors in EOP may represent a novel approach for monitoring children with EOP.


A) Evoked Heat Pain Response in fMRI. Clusters of significantly greater activation in the Putamen and Caudate in children with EOP (N=23) compared to HCs (N=20) with mixed-Effects (FLAME1) FSL analysis corrected for age and sex (cluster-size corrected p < 0.05). 5/10 temperature in scanner mean (SD) EOP=42.8(2.7), HC=43.7(2.1) °C. Subject-specific parameter estimates extracted from the left putamen and caudate clusters, demonstrating higher parameter estimates in children with EOP compared to HCs. B) Resting-state fMRI Connectivity. Seed-based resting-state fMRI analyses revealed clusters of higher connectivity from left and right thalamus seeds to somatosensory cortex regions and the contralateral putamen (blue clusters) in children with EOP (N = 24) compared to HCs (N = 20), cluster-size threshold p<0.001 p-FDR corrected for multiple comparisons and adjusted for age and sex. Parameter estimates were extracted from whole-ROI-to-ROI connectivity to demonstrate higher functional connectivity between the thalamus and the putamen, and between the thalamus and the precentral gyrus, in children with EOP compared to HCs. C) Striatal connectopic mapping second-order connectivity mode [indicative of Striatal Dopamine Transporter Density] of the putamen and caudate nucleus accumens (CNA) overlayed on an MNI template brain. Trend Surface Modelling (TSM) shows higher TSM coefficients for the left caudate (Y) and a trend for the left putamen (Y3) in children with EOP compared to HCs.

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