A combined DTI and resting state functional MRI study in patients with postherpetic neuralgia.

Purpose: To explore the brain microstructural and functional changes in patients with postherpetic neuralgia (PHN).Materials and Methods: 12 PHN patients and 12 healthy volunteers were enrolled. Diffusion tensor imaging (DTI) and resting-state functional MRI (rfMRI) sequences were scanned by a 3T MR...

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Detalles Bibliográficos
Publicado en:Japanese Journal of Radiology Vol. 38; no. 5; pp. 440 - 451
Autores principales: Dai, Hui, Jiang, Chengcheng, Wu, Guanzuan, Huang, Renjun, Jin, Xiaohong, Zhang, Zhongshuai, Wang, Lina, Li, Yonggang
Formato: diagnostic images research tables/charts Journal Article
Publicado: Springer Nature May2020
Acceso en línea:Ver este registro en EBSCOhost
Descripción
Sumario:Purpose: To explore the brain microstructural and functional changes in patients with postherpetic neuralgia (PHN).Materials and Methods: 12 PHN patients and 12 healthy volunteers were enrolled. Diffusion tensor imaging (DTI) and resting-state functional MRI (rfMRI) sequences were scanned by a 3T MR scanner. Fractional anisotropy (FA) and mean diffusivity (MD) t-maps were obtained following DTI data processing. The amplitude of low-frequency fluctuation (ALFF) and fractional ALFF (fALFF) were obtained following rfMRI data processing. A two sample t-test was performed to compare the FA, MD, ALFF and fALFF differences between the PHN patients and healthy controls.Results: No significant differences were noted with regard to the parameters gender, age and education years between the two groups. FA, MD, ALFF and/or fALFF indicated significant alterations in specific pain or pain-related brain regions, such as brainstem, cerebellum, parietal lobe, precuneus, frontal lobe, temporal lobe, postcentral and precentral gyrus, corpus callosum, cingulate gyrus, putamen and insula.Conclusion: Multi-local alterations of spontaneous brain activity could form a network related to chronic pain, sensory discrimination, emotion and cognition, suggesting complicated central mechanisms of PHN. The combined-action of brain microstructure and function may play a critical role in comprehension of neurological mechanisms of PHN-induced pain.