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. 2015 Oct 23;10(10):e0141133.
doi: 10.1371/journal.pone.0141133. eCollection 2015.

A Functional Magnetic Resonance Imaging Study to Investigate the Utility of a Picture Imagination Task in Investigating Neural Responses in Patients with Chronic Musculoskeletal Pain to Daily Physical Activity Photographs

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A Functional Magnetic Resonance Imaging Study to Investigate the Utility of a Picture Imagination Task in Investigating Neural Responses in Patients with Chronic Musculoskeletal Pain to Daily Physical Activity Photographs

Ann M Taylor et al. PLoS One. .

Abstract

Pain-related anxiety and fear are associated with increased difficulties in attention, increased awareness of pain, impaired disengagement from pain, and can moderate the effects of attentional coping attempts. Accurately assessing the direct impact of pain-related anxiety and fear on pain behavior has proved difficult. Studies have demonstrated no or limited influence of pain-related fear and anxiety on behavior but this may be due to inherent problems with the scales used. Neuroimaging has improved the understanding of neural processes underlying the factors that influence pain perception. This study aimed to establish if a Picture and Imagination Task (PIT), largely developed from the Photographs of Daily Activity (PHODA) assessment tool, could help explore how people living with chronic pain process information about daily activities. Blood oxygenation level dependent (BOLD) functional magnetic resonance imaging (fMRI) was used to compare brain responses in patients with chronic musculoskeletal pain (CMSKP) (n = 15) and healthy controls (n = 15). Subjects were asked to imagine how they would feel mentally and physically if asked to perform daily activities illustrated in PIT. The results found that a number of regions involved in pain processing saw increased BOLD activation in patients compared with controls when undertaking the task and included the insula, anterior cingulate cortex, thalamus and inferior and superior parietal cortices. Similarly, increased BOLD responses in patients compared to controls in the frontal pole, paracingulate and the supplementary motor cortex may be suggestive of a memory component to the responses The amygdala, orbitofrontal cortex, substantia nigra/ventral tegmentum, putamen, thalamus, pallidum, inferior parietal (supramarginal and angular gyrus) and cingulate cortex were also seen to have greater differences in BOLD signal changes in patients compared with controls and many of these regions are also associated with general phobic responses. Therefore, we suggest that PIT is a useful task to explore pain- and movement-related anxiety and fear in fMRI studies. Regions in the Default Mode Network remained active or were less deactivated during the PIT task in patients with CMSKP compared to healthy controls supporting the contention that the DMN is abnormal in patients with CMSKP.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1
Fig 1. Trial timing.
Each trial in the task lasted 7–15 s and was composed of 4 different screens; a photo from either PHODA or a resting activity, a fixation cross, a screen to indicate the subject should respond and ended with a second fixation cross.
Fig 2
Fig 2. Maps illustrating activation of brain regions during the PIT task activity.
Statistical maps of the patient group, the control group and patient > control comparing activation during the PIT task. Patients with CMSKP have significantly different BOLD activation in regions known to be involved in pain processing, phobia and fear conditioning. Each z-statistic map represents these group differences in a whole brain analysis. The color bar shows the scale of the Z-statistic (2.3–8.1). Slice location is identified in white on the figures and presented in millimeters. The z-stat comes from the corrected clusters, the z-stats themselves are not corrected. PCC: posterior cingulate cortex, ACC: anterior cingulate cortex, STG: superior temporal gyrus, OFG: orbitofrontal gyrus, SN/VT: substantia nigra/ventral tegmental region, IFG: inferior frontal gyrus.
Fig 3
Fig 3. Graphs illustrating the percentage signal change in areas illustrated in Fig 2.
The graphs show the percentage signal change with the error bars representing standard deviations across subjects. The percent signal change is calculated across the significantly activated voxels within the Harvard-Oxford atlas defined anatomical region. Images illustrated in Fig 2 are a combination of anatomical and functional data and the graphs represent the direction and magnitude of the signal change within the regions illustrated in Fig 2 Because these activations are already defined as significant, no further statistical tests were performed.

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