Increased power spectral density in resting-state pain-related brain
networks in fibromyalgia
    
    
    
- Author(s)
- Ji-Young Kim; Seong-Ho Kim; Jeehye Seo; Sang-Hyon Kim; Seung Woo Han; Eon Jeong Nam; Seong-Kyu Kim; Hui Joong Lee; Seung-Jae Lee; Yang-Tae Kim; Yongmin Chang
- Keimyung Author(s)
- Kim, Sang Hyon; Kim, Yang Tae
- Department
- Dept. of Internal Medicine (내과학)
 Dept. of Psychiatry (정신건강의학)
- Journal Title
- Pain
- Issued Date
- 2013
- Volume
- 154
- Issue
- 9
- Abstract
- Fibromyalgia (FM), characterized by chronic widespread pain, is known to be associated with heightened
 responses to painful stimuli and atypical resting-state functional connectivity among pain-related
 regions of the brain. Previous studies of FM using resting-state functional magnetic resonance imaging
 (rs-fMRI) have focused on intrinsic functional connectivity, which maps the spatial distribution of temporal
 correlations among spontaneous low-frequency fluctuation in functional MRI (fMRI) resting-state
 data. In the current study, using rs-fMRI data in the frequency domain, we investigated the possible alteration
 of power spectral density (PSD) of low-frequency fluctuation in brain regions associated with central
 pain processing in patients with FM. rsfMRI data were obtained from 19 patients with FM and 20 agematched
 healthy female control subjects. For each subject, the PSDs for each brain region identified from
 functional connectivity maps were computed for the frequency band of 0.01 to 0.25 Hz. For each group,
 the average PSD was determined for each brain region and a 2-sample t test was performed to determine
 the difference in power between the 2 groups. According to the results, patients with FM exhibited significantly
 increased frequency power in the primary somatosensory cortex (S1), supplementary motor
 area (SMA), dorsolateral prefrontal cortex, and amygdala. In patients with FM, the increase in PSD did
 not show an association with depression or anxiety. Therefore, our findings of atypical increased frequency
 power during the resting state in pain-related brain regions may implicate the enhanced resting-
 state baseline neural activity in several brain regions associated with pain processing in FM.
 
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