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Chronic Post-Ischemia Pain Model for Complex Regional Pain Syndrome Type-I in Rats
Published on: January 21, 2020
fMRI reveals distinct CNS processing during symptomatic and recovered complex regional pain syndrome in children
1P.A.I.N. Group, Department of Anesthesia, Children's Hospital Boston, MA, USA.
Insights
Paediatric Complex Regional Pain Syndrome (CRPS) shows distinct central nervous system (CNS) activation patterns, even after recovery. These brain changes in children with CRPS suggest altered circuitry persists, impacting how they process stimuli.
Area of Science:
- Neuroscience
- Paediatric Medicine
- Pain Research
Background:
- Complex Regional Pain Syndrome (CRPS) in children differs from adult presentations, often resolving completely.
- Paediatric CRPS offers a unique model to study pain mechanisms due to the ability to compare symptomatic and asymptomatic states within individuals.
- Understanding the central nervous system (CNS) role in paediatric CRPS is crucial for developing targeted treatments.
Purpose of the Study:
- To investigate CNS activation patterns using functional magnetic resonance imaging (fMRI) in paediatric patients with lower extremity CRPS.
- To compare brain activity during active pain (CRPS(+)) and after recovery (CRPS(-)) using both affected and unaffected limb stimulation.
- To identify neural correlates of CRPS symptoms and understand the long-term impact on brain circuitry.
Main Methods:
- fMRI scans were conducted on paediatric patients (9-18 years) during active CRPS and after recovery.
- Mechanical (brush) and thermal (cold) stimuli were applied to affected and unaffected limbs.
- Within-group and between-group analyses compared CNS activation patterns between different states and limbs.
Main Results:
- During active CRPS, stimuli causing allodynia showed CNS activation patterns similar to adult CRPS.
- Painful stimuli induced decreased BOLD signal, indicating activation of endogenous pain modulation.
- Persistent activation differences were observed in recovered patients, suggesting lasting CNS changes.
- Altered brain responses to non-noxious stimuli in unaffected limbs indicate a 'CRPS brain' phenotype.
Conclusions:
- Paediatric CRPS is associated with significant and persistent changes in CNS circuitry.
- These alterations may explain various CRPS symptoms, including movement disorders and sensory processing deficits.
- The findings highlight the importance of considering CNS involvement in the long-term management of paediatric CRPS.
Abstract:
Complex regional pain syndrome (CRPS) in paediatric patients is clinically distinct from the adult condition in which there is often complete resolution of its signs and symptoms within several months to a few years. The ability to compare the symptomatic and asymptomatic condition in the same individuals makes this population interesting for the investigation of mechanisms underlying pain and other symptoms of CRPS. We used fMRI to evaluate CNS activation in paediatric patients (9-18 years) with CRPS affecting the lower extremity. Each patient underwent two scanning sessions: once during an active period of pain (CRPS(+)), and once after symptomatic recovery (CRPS(-)). In each session, mechanical (brush) and thermal (cold) stimuli were applied to the affected region of the involved limb and the corresponding mirror region of the unaffected limb. Two fundamental fMRI analyses were performed: (i) within-group analysis for CRPS(+) state and CRPS(-) state for brush and cold for the affected and unaffected limbs in each case; (ii) between-group (contrast) analysis for activations in affected and unaffected limbs in CRPS or post-CRPS states. We found: (i) in the CRPS(+) state, stimuli that evoked mechanical or cold allodynia produced patterns of CNS activation similar to those reported in adult CRPS; (ii) in the CRPS(+) state, stimuli that evoked mechanical or cold allodynia produced significant decreases in BOLD signal, suggesting pain-induced activation of endogenous pain modulatory systems; (iii) cold- or brush-induced activations in regions such as the basal ganglia and parietal lobe may explain some CNS-related symptoms in CRPS, including movement disorders and hemineglect/inattention; (iv) in the CRPS(-) state, significant activation differences persisted despite nearly complete elimination of evoked pain; (v) although non-noxious stimuli to the unaffected limb were perceived as equivalent in CRPS(+) and CRPS(-) states, the same stimulus produced different patterns of activation in the two states, suggesting that the 'CRPS brain' responds differently to normal stimuli applied to unaffected regions. Our results suggest significant changes in CNS circuitry in patients with CRPS.
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