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Volume 183, Issue 2, Pages 99-104 (30 August 2010)


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Functional magnetic resonance imaging response to experimental pain in drug-free patients with schizophrenia

Camilo de la Fuente-Sandovalab, Rafael Favilac, Diana Gómez-Martind, Francisco Pellicere, Ariel Graff-GuerrerofCorresponding Author Informationemail address

Received 25 May 2009; received in revised form 6 February 2010; accepted 6 May 2010.

Abstract 

Clinical evidence suggests that there is decreased pain sensitivity in schizophrenia; however, the neurobiological mechanism of this decrease remains unknown. Using functional magnetic resonance imaging, we examined the blood oxygen level-dependent (BOLD) changes induced by experimental pain-tolerance (endure) hot stimuli vs. non-painful stimuli during an acute psychotic episode in 12 drug-free patients with schizophrenia and in 13 gender- and age-matched healthy controls. The analyses revealed that patients showed a greater BOLD response at S1 compared with controls but a reduced BOLD response in the posterior cingulate cortex (PCC), insula, and brainstem during pain-tolerance stimuli. Pain-tolerance temperature was higher in patients than in healthy controls. BOLD response in the insula positively correlated with unpleasantness and temperature in controls, but this effect was not observed in patients. S1 BOLD response positively correlated with unpleasantness in patients but not in controls. These initial results confirm that unmedicated patients with schizophrenia have a higher pain tolerance than controls, decreased activation in pain affective–cognitive processing regions (insula, PCC, brainstem), and an over-activation of the primary sensory-discriminative pain processing region (S1). These pilot results are the first to explore the mechanism driving altered pain sensitivity in schizophrenia.

a Laboratorio de Psiquiatría Experimental, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico

b Departamento de Neuropsiquiatría, Instituto Nacional de Neurología y Neurocirugía, Mexico City, Mexico

c MR Advanced Applications, GE Healthcare, Mexico City, Mexico

d Departamento de Inmunología y Reumatología, Instituto Nacional de Nutrición, Mexico City, Mexico

e Laboratorio de Neurofisiología Integrativa, Instituto Nacional de Psiquiatría, Mexico City, Mexico

f Multimodal Neuroimaging Schizophrenia Group, PET Centre, Centre for Addiction and Mental Health, 250 College Street, Toronto, Ontario, Canada M5T 1R8

Corresponding Author InformationCorresponding author.

PII: S0925-4927(10)00159-9

doi:10.1016/j.pscychresns.2010.05.003


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