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Resting-State Magnetoencephalography Reveals Neurobiological Bridges Between Pain and Cognitive Impairment

INTRODUCTION: Pain has been identified as a risk factor for cognitive dysfunction, which in turn affects pain perception. Although pain, cognitive dysfunction, and their interaction are clinically important, the neural mechanism connecting the two phenomena remains unclear. METHODS: The resting-stat...

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Detalles Bibliográficos
Autores principales: Shigihara, Yoshihito, Hoshi, Hideyuki, Fukasawa, Keisuke, Ichikawa, Sayuri, Kobayashi, Momoko, Sakamoto, Yuki, Negishi, Kazuyuki, Haraguchi, Rika, Konno, Shin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8119570/
https://www.ncbi.nlm.nih.gov/pubmed/33095348
http://dx.doi.org/10.1007/s40122-020-00213-0
Descripción
Sumario:INTRODUCTION: Pain has been identified as a risk factor for cognitive dysfunction, which in turn affects pain perception. Although pain, cognitive dysfunction, and their interaction are clinically important, the neural mechanism connecting the two phenomena remains unclear. METHODS: The resting-state brain activity of 38 participants was measured using magnetoencephalography before and after the patients underwent selective nerve root block (SNRB) for the treatment of their pain. We then assessed the extent to which these data correlated with the subjective levels of pain experienced by the patients across SNRB based on the visual analogue scale and the cognitive status of the patients measured after SNRB using the Japanese versions of the Mini-Mental State Examination (MMSE-J). RESULTS: Slow oscillations (delta) in the right precentral gyrus, right middle temporal gyrus, and left superior frontal gyrus were negatively correlated with the subjective level of pain, and fast oscillations (gamma) in the right insular cortex and right middle temporal gyrus before SNRB were negatively correlated with the MMSE-J score afterwards. These correlations disappeared after SNRB. CONCLUSION: The presently observed changes in neural activity, as indicated by oscillation changes, might represent the transient bridge between pain and cognitive dysfunction in patients with severe pain. Our findings underscore the importance of treating pain before a transient diminishment of cognitive function becomes persistent.