학술논문

Altered parietal operculum cortex 2 functional connectivity in benign paroxysmal positional vertigo patients with residual dizziness: A resting‐state fMRI study.
Document Type
Article
Source
CNS Neuroscience & Therapeutics. Feb2024, Vol. 30 Issue 2, p1-10. 10p.
Subject
*BENIGN paroxysmal positional vertigo
*PARIETAL lobe
*FUNCTIONAL connectivity
*FUNCTIONAL magnetic resonance imaging
*PREFRONTAL cortex
*TEMPORAL lobe
Language
ISSN
1755-5930
Abstract
Aims: To investigate changes in functional connectivity (FC) focusing on parietal operculum cortex 2 (OP2) in benign paroxysmal positional vertigo (BPPV) patients with residual dizziness (RD) after successful canalith repositioning procedure (CRP). Methods: High‐resolution three‐dimensional T1 and resting‐state functional magnetic resonance imaging (fMRI) were performed on 55 healthy controls (HCs), 55 BPPV patients with RD, and 55 patients without RD after successful CRP. Seed‐based (bilateral OP2) FC was calculated to investigate the changes in FC among the three groups. Additionally, we further explored the associations between abnormal FC and clinical symptoms. Results: One‐way analysis of covariance showed significant FC differences among the three groups. Post‐hoc analysis showed that patients with RD exhibited decreased FC between left OP2 and regions of left angular gyrus (AG), thalamus, precuneus, middle frontal gyrus (MFG), and right cerebellum posterior lobe (CPL) in comparison with HCs. In addition, compared with patients without RD, patients with RD showed decreased FC between left OP2 and regions of left MFG, AG, middle temporal gyrus, and right CPL. Moreover, in patients with RD, the FC between left thalamus and OP2 was negatively correlated with duration of RD, and the FC between left AG and OP2 was negatively correlated with duration of BPPV. Conclusion: BPPV patients with RD showed reduced FC between brain regions involved in vestibular processing and spatial cognition; These results suggested that BPPV patients with RD might have diminished central processing of vestibular information and impaired spatial cognition. [ABSTRACT FROM AUTHOR]