Age-associated alterations in thalamocortical structural connectivity in youths with a psychosis-spectrum disorder.
Lydia LewisMary CorcoranKang Ik K ChoYooBin KwakRebecca A HayesBart LarsenMaria JalbrzikowskiPublished in: Schizophrenia (Heidelberg, Germany) (2023)
Psychotic symptoms typically emerge in adolescence. Age-associated thalamocortical connectivity differences in psychosis remain unclear. We analyzed diffusion-weighted imaging data from 1254 participants 8-23 years old (typically developing (TD):N = 626, psychosis-spectrum (PS): N = 329, other psychopathology (OP): N = 299) from the Philadelphia Neurodevelopmental Cohort. We modeled thalamocortical tracts using deterministic fiber tractography, extracted Q-Space Diffeomorphic Reconstruction (QSDR) and diffusion tensor imaging (DTI) measures, and then used generalized additive models to determine group and age-associated thalamocortical connectivity differences. Compared to other groups, PS exhibited thalamocortical reductions in QSDR global fractional anisotropy (GFA, p-values range = 3.0 × 10 -6 -0.05) and DTI fractional anisotropy (FA, p-values range = 4.2 × 10 -4 -0.03). Compared to TD, PS exhibited shallower thalamus-prefrontal age-associated increases in GFA and FA during mid-childhood, but steeper age-associated increases during adolescence. TD and OP exhibited decreases in thalamus-frontal mean and radial diffusivities during adolescence; PS did not. Altered developmental trajectories of thalamocortical connectivity may contribute to the disruptions observed in adults with psychosis.
Keyphrases
- white matter
- functional connectivity
- resting state
- depressive symptoms
- diffusion weighted imaging
- acute lymphoblastic leukemia
- working memory
- magnetic resonance imaging
- bipolar disorder
- physical activity
- multiple sclerosis
- machine learning
- computed tomography
- magnetic resonance
- deep brain stimulation
- contrast enhanced
- ultrasound guided
- early life
- childhood cancer