Altered cortical excitability in persistent idiopathic facial pain.


Journal

Cephalalgia : an international journal of headache
ISSN: 1468-2982
Titre abrégé: Cephalalgia
Pays: England
ID NLM: 8200710

Informations de publication

Date de publication:
02 2019
Historique:
pubmed: 15 6 2018
medline: 14 4 2020
entrez: 15 6 2018
Statut: ppublish

Résumé

Persistent idiopathic facial pain is a refractory and disabling condition of unknown mechanism and etiology. It has been suggested that persistent idiopathic facial pain patients have not only peripheral generators of pain, but also central nervous system changes that would contribute to the persistence of symptoms. We hypothesized that persistent idiopathic facial pain would have changes in brain cortical excitability as measured by transcranial magnetic stimulation compared to healthy controls. Twenty-nine persistent idiopathic facial pain patients were compared to age- and sex-matched healthy controls and underwent cortical excitability measurements by transcranial magnetic stimulation applied to the cortical representation of the masseter muscle of both hemispheres. Single-pulse stimulation was used to measure the resting motor threshold and suprathreshold motor-evoked potentials. Paired-pulse stimulation was used to assess short intracortical inhibition and intracortical facilitation. Clinical pain and associated symptoms were assessed with validated tools. Spontaneous pain was found in 27 (93.1%) and provoked pain was found in two (6.9%) persistent idiopathic facial pain patients. The motor-evoked potentials at 120% and 140% were significantly lower for both hemispheres compared to controls. Persistent idiopathic facial pain patients had lower short-interval intracortical inhibition compared with controls. These changes were correlated with some aspects of quality of life, and higher mood symptoms. These neurophysiological alterations were not influenced by analgesic medication, as similar changes were observed in patients with or without central-acting drugs. Persistent idiopathic facial pain is associated with changes in intracortical modulation involving GABAergic mechanisms, which may be related to certain aspects of the pathophysiology of this chronic pain condition. Trial registration: NTC01746355.

Identifiants

pubmed: 29898612
doi: 10.1177/0333102418780426
doi:

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

219-228

Auteurs

Ricardo Galhardoni (R)

1 Pain Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.
2 Service of Interdisciplinary Neuromodulation (SIN), Laboratory of Neurosciences (LIM-27), Department and Institute of Psychiatry, University of São Paulo, São Paulo, Brazil.
3 School of Medicine, University of City of São Paulo (UNICID), São Paulo, Brazil.

Daniel Ciampi de Andrade (D)

1 Pain Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.
2 Service of Interdisciplinary Neuromodulation (SIN), Laboratory of Neurosciences (LIM-27), Department and Institute of Psychiatry, University of São Paulo, São Paulo, Brazil.
4 Pain Center, Cancer Institute of State of São Paulo "Octavio Frias de Oliveira", São Paulo, Brazil.

Mariana Yt Puerta (MY)

1 Pain Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Andre R Brunoni (AR)

2 Service of Interdisciplinary Neuromodulation (SIN), Laboratory of Neurosciences (LIM-27), Department and Institute of Psychiatry, University of São Paulo, São Paulo, Brazil.

Bruna Lr Varotto (BL)

1 Pain Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.
5 Dentistry Division of the Central Institute and Experimental Neurosurgery Division of the Psychiatric Institute, Clinics Hospital, School of Medicine, University of São Paulo, São Paulo SP, Brazil.

José Tt de Siqueira (JT)

1 Pain Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.
5 Dentistry Division of the Central Institute and Experimental Neurosurgery Division of the Psychiatric Institute, Clinics Hospital, School of Medicine, University of São Paulo, São Paulo SP, Brazil.

Manoel J Teixeira (MJ)

1 Pain Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.
2 Service of Interdisciplinary Neuromodulation (SIN), Laboratory of Neurosciences (LIM-27), Department and Institute of Psychiatry, University of São Paulo, São Paulo, Brazil.
4 Pain Center, Cancer Institute of State of São Paulo "Octavio Frias de Oliveira", São Paulo, Brazil.
6 Neurosurgery Division, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.

Silvia Rdt Siqueira (SR)

1 Pain Center, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.
5 Dentistry Division of the Central Institute and Experimental Neurosurgery Division of the Psychiatric Institute, Clinics Hospital, School of Medicine, University of São Paulo, São Paulo SP, Brazil.
6 Neurosurgery Division, Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil.
7 School of Arts, Science and Humanities, University of São Paulo, São Paulo, Brazil.

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Classifications MeSH