Adolescents’ pain-related ontogeny shares a neural basis with adults’ chronic pain in basothalamo-cortical organization
During late adolescence, the brain undergoes ontogenic organization altering subcortical-cortical circuitry. This includes regions implicated in pain chronicity, and thus alterations in the adolescent ontogenic organization could predispose to pain chronicity in adulthood - however, evidence is lack...
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Veröffentlicht in: | iScience 2024-02, Vol.27 (2), p.108954-108954, Article 108954 |
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Sprache: | eng |
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Zusammenfassung: | During late adolescence, the brain undergoes ontogenic organization altering subcortical-cortical circuitry. This includes regions implicated in pain chronicity, and thus alterations in the adolescent ontogenic organization could predispose to pain chronicity in adulthood - however, evidence is lacking. Using resting-state functional magnetic resonance imaging from a large European longitudinal adolescent cohort and an adult cohort with and without chronic pain, we examined links between painful symptoms and brain connectivity. During late adolescence, thalamo-, caudate-, and red nucleus-cortical connectivity were positively and subthalamo-cortical connectivity negatively associated with painful symptoms. Thalamo-cortical connectivity, but also subthalamo-cortical connectivity, was increased in adults with chronic pain compared to healthy controls. Our results indicate a shared basis in basothalamo-cortical circuitries between adolescent painful symptomatology and adult pain chronicity, with the subthalamic pathway being differentially involved, potentially due to a hyperconnected thalamo-cortical pathway in chronic pain and ontogeny-driven organization. This can inform neuromodulation-based prevention and early intervention.
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•Adolescent ontogenic basothalamo-cortical changes and painful symptoms correlate•Basothalamo-cortical brain connectivity is altered in adult chronic pain•The overlapping neural basis indicates complex brain-pain trajectories•Late adolescence may be a sensitive period of pain-related brain changes
Neuroscience; Clinical neuroscience; Sensory neuroscience |
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ISSN: | 2589-0042 2589-0042 |
DOI: | 10.1016/j.isci.2024.108954 |