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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.

Authors :
Liu, Huanxian
Liu, Jiajin
Sun, Shuping
Dai, Wei
Nie, Binbin
Xu, Baixuan
Dong, Zhao
Yu, Shengyuan
Source :
International Journal of Neuroscience. Jun2024, Vol. 134 Issue 6, p543-550. 8p.
Publication Year :
2024

Abstract

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. 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. 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. 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. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00207454
Volume :
134
Issue :
6
Database :
Academic Search Index
Journal :
International Journal of Neuroscience
Publication Type :
Academic Journal
Accession number :
177520057
Full Text :
https://doi.org/10.1080/00207454.2022.2126773