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Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study

Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by motor and nonmotor signs and symptoms. To date, many studies of PD have focused on its cardinal motor symptoms. To study the nonmotor signs of early PD, we investigated the reactions solicited by heat pain stim...

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Autores principales: Tan, Ying, Tan, Juan, Luo, Cheng, Cui, Wenjuan, He, Hui, Bin, Yi, Deng, Jiayan, Tan, Rui, Tan, Wenrong, Liu, Tao, Zeng, Nanlin, Xiao, Ruhui, Yao, Dezhong, Wang, Xiaoming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299805/
https://www.ncbi.nlm.nih.gov/pubmed/25628915
http://dx.doi.org/10.1155/2015/273019
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author Tan, Ying
Tan, Juan
Luo, Cheng
Cui, Wenjuan
He, Hui
Bin, Yi
Deng, Jiayan
Tan, Rui
Tan, Wenrong
Liu, Tao
Zeng, Nanlin
Xiao, Ruhui
Yao, Dezhong
Wang, Xiaoming
author_facet Tan, Ying
Tan, Juan
Luo, Cheng
Cui, Wenjuan
He, Hui
Bin, Yi
Deng, Jiayan
Tan, Rui
Tan, Wenrong
Liu, Tao
Zeng, Nanlin
Xiao, Ruhui
Yao, Dezhong
Wang, Xiaoming
author_sort Tan, Ying
collection PubMed
description Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by motor and nonmotor signs and symptoms. To date, many studies of PD have focused on its cardinal motor symptoms. To study the nonmotor signs of early PD, we investigated the reactions solicited by heat pain stimuli in early untreated PD patients without pain using fMRI. The activation patterns of contact heat stimuli (51°C) were assessed in 14 patients and 17 age- and sex-matched healthy controls. Patients with PD showed significant decreases in activation of the superior temporal gyrus (STG) and insula compared with controls. In addition, a significant relationship between activation of the insula and STG and the pain scores was observed in healthy controls but not in PD. This study provided further support that the insula and STG are important parts of the somatosensory circuitry recruited during the period of pain. The hypoactivity of the STG and insula in PD implied that functions including affective, cognitive, and sensory-discriminative processes, which are associated with the insula and STG, were disturbed. This finding supports the view that leaving early PD untreated could be tied directly to central nervous system dysfunction.
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spelling pubmed-42998052015-01-27 Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study Tan, Ying Tan, Juan Luo, Cheng Cui, Wenjuan He, Hui Bin, Yi Deng, Jiayan Tan, Rui Tan, Wenrong Liu, Tao Zeng, Nanlin Xiao, Ruhui Yao, Dezhong Wang, Xiaoming Parkinsons Dis Research Article Parkinson's disease (PD) is a progressive neurodegenerative disease characterized by motor and nonmotor signs and symptoms. To date, many studies of PD have focused on its cardinal motor symptoms. To study the nonmotor signs of early PD, we investigated the reactions solicited by heat pain stimuli in early untreated PD patients without pain using fMRI. The activation patterns of contact heat stimuli (51°C) were assessed in 14 patients and 17 age- and sex-matched healthy controls. Patients with PD showed significant decreases in activation of the superior temporal gyrus (STG) and insula compared with controls. In addition, a significant relationship between activation of the insula and STG and the pain scores was observed in healthy controls but not in PD. This study provided further support that the insula and STG are important parts of the somatosensory circuitry recruited during the period of pain. The hypoactivity of the STG and insula in PD implied that functions including affective, cognitive, and sensory-discriminative processes, which are associated with the insula and STG, were disturbed. This finding supports the view that leaving early PD untreated could be tied directly to central nervous system dysfunction. Hindawi Publishing Corporation 2015 2015-01-05 /pmc/articles/PMC4299805/ /pubmed/25628915 http://dx.doi.org/10.1155/2015/273019 Text en Copyright © 2015 Ying Tan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tan, Ying
Tan, Juan
Luo, Cheng
Cui, Wenjuan
He, Hui
Bin, Yi
Deng, Jiayan
Tan, Rui
Tan, Wenrong
Liu, Tao
Zeng, Nanlin
Xiao, Ruhui
Yao, Dezhong
Wang, Xiaoming
Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study
title Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study
title_full Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study
title_fullStr Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study
title_full_unstemmed Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study
title_short Altered Brain Activation in Early Drug-Naive Parkinson's Disease during Heat Pain Stimuli: An fMRI Study
title_sort altered brain activation in early drug-naive parkinson's disease during heat pain stimuli: an fmri study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4299805/
https://www.ncbi.nlm.nih.gov/pubmed/25628915
http://dx.doi.org/10.1155/2015/273019
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