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Medication overuse headache associated with decreased dopamine transporter availability in the medial but not in the lateral orbitofrontal cortex: a 11CFT PET/MR study.
Liu, Huanxian; Liu, Jiajin; Sun, Shuping; Dai, Wei; Nie, Binbin; Xu, Baixuan; Dong, Zhao; Yu, Shengyuan.
Afiliação
  • Liu H; Department of Neurology, Chinese PLA General Hospital, Beijing, China.
  • Liu J; Medical School of Chinese PLA, Beijing, China.
  • Sun S; Department of Nuclear Medicine, First Medical Center, Chinese PLA General Hospital, Beijing, China.
  • Dai W; Department of Neurology, Chinese PLA General Hospital, Beijing, China.
  • Nie B; Medical School of Chinese PLA, Beijing, China.
  • Xu B; Department of Neurology, Chinese PLA General Hospital, Beijing, China.
  • Dong Z; Medical School of Chinese PLA, Beijing, China.
  • Yu S; Beijing Engineering Research Center of Radiographic Techniques and Equipment, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, China.
Int J Neurosci ; : 1-8, 2022 Sep 24.
Article em En | MEDLINE | ID: mdl-36120989
BACKGROUNDS: Dysfunction of the mesocorticolimbic dopamine system in medication overuse headache (MOH) is unknown. This study aimed to determine dopamine transporter (DAT) availability, which is sensitive to dopamine levels, in the mesocorticolimbic dopamine system in MOH patients. METHODS: This case-control study investigated eligible MOH patients admitted to the International Headache Centre in the neurological department of Chinese PLA General Hospital between July 2018 and August 2019. All subjects underwent an integrated positron emission tomography (PET)/magnetic resonance (MR) brain scans with 11CFT, a radioligand that binds to DAT. Standardised uptake value ratio (SUVr) images were compared voxelwise between MOH patients and healthy controls (HCs). SUVr values from significantly changed regions were extracted, and partial correlation analyses with clinical measures were conducted. RESULTS: We examined 17 MOH patients and 16 HCs. MOH patients had lower SUVr levels in the medial rather than lateral orbitofrontal cortex (OFC) than HCs (T = -5.0317, PGRF < 0.01), which showed no correlation with clinical features. CONCLUSIONS: MOH is characterised by decreased DAT availability in the medial OFC, which might reflect compensatory downregulation due to low dopamine signalling within the mesocorticolimbic dopamine system and provide a new perspective to understand the pathogenesis of MOH.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Risk_factors_studies Idioma: En Ano de publicação: 2022 Tipo de documento: Article