Back to Search Start Over

Neurometabolic and Brain Functional Alterations Associated with Cognitive Impairment in Patients with Myasthenia Gravis: A Combined 1H-MRS and fMRI Study.

Authors :
Zhou, Xiaoling
Yang, Yang
Zhu, Feng
Chen, Xiang
Zhu, Yunfei
Gui, Tiantian
Li, Yonggang
Xue, Qun
Source :
Neuroscience. Apr2024, Vol. 544, p12-27. 16p.
Publication Year :
2024

Abstract

• MG patients were accompanied by cognitive decline. • MG patients have a combination of abnormal brain function and neurometabolites. • First study of investigating neurometabolites in vivo in patients with MG. Whether patients with myasthenia gravis (MG) exhibit cognitive impairment is controversial. Also the underlying mechanisms are unknown. We aimed to investigate alterations in cognitive function, neurometabolite levels, and brain function in patients with MG and to explore the associations between abnormal regional brain functional activity, neurometabolite concentrations in the MPFC and left thalamus, and cognitive activity in patients with MG. Neuropsychological tests, proton magnetic resonance spectroscopy, and resting-state functional magnetic resonance imaging were performed on 41 patients with MG and 45 race-, sex-, age-, and education-matched healthy controls (HCs). The results suggest that MG is accompanied by cognitive decline, as indicated by global cognitive function, visual-spatial function, language, memory, abnormalities in regional brain functional activity, and neurometabolite alterations (including GABA, NAA, and Cho) in the medial prefrontal cortex (MPFC) and left thalamus. Cognitive impairment in patients with MG may be related to abnormal regional brain functional activity and changes in neurometabolites, and regional brain functional activity may be modulated by specific neurometabolites. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03064522
Volume :
544
Database :
Academic Search Index
Journal :
Neuroscience
Publication Type :
Academic Journal
Accession number :
176435412
Full Text :
https://doi.org/10.1016/j.neuroscience.2024.02.021