PCA-Logistic regression analysis of relative volume changes of brain structure and gait disorders in patients with small vessel disease
Discuss this preprint
Start a discussion What are Sciety discussions?Listed in
This article is not in any list yet, why not save it to one of your lists.Abstract
Aims To investigate the relationship between the relative volume changes of brain structures and gait disorders in patients with cerebral small vessel disease (CSVD), and to identify key brain volume indicators that influence gait disorders (GD) through principal component analysis (PCA) combined with logistic regression analysis. Methods A total of 90 patients with CSVD were included and divided into two groups based on their Timed Up and Go Test (TUG) results: the CSVD gait disorder group (GD group, N=50, TUG ≥ 11.5 seconds) and the CSVD non-gait disorder group (NGD group, N=40, TUG < 11.5 seconds). Brain structural volumes and associated imaging markers were calculated using a 3.0T superconducting magnetic resonance imaging (MRI) system combined with an intelligent image analysis platform. The relative volume data of brain structures were subjected to PCA for dimensionality reduction. Regression analysis of the principal components was performed to identify key predictive indicators for gait disorders. Results Principal components 2 and 3 exhibited significant predictive power for gait disorders. Component 2 primarily represented cerebrospinal fluid, the temporal lobe, and the frontal lobe, while Component 3 primarily represented the third ventricle, lateral ventricle, and corpus callosum. Analysis of component loadings indicated that the expansion of cerebrospinal fluid-related structures was positively correlated with the severity of gait disorders, while atrophy of brain tissue structures showed a negative correlation. No significant difference was observed in the total CSVD burden score between the GD and NGD groups. Conclusion The enlargement of the cerebrospinal fluid spaces and the ventricular system are key factors contributing to gait disorders in CSVD patients. Additionally, atrophy in cortical areas such as the temporal and frontal lobes, as well as the corpus callosum, plays a predictive role in the severity of gait disturbances. The total CSVD burden score does not adequately reflect the degree of gait impairment and requires further refinement for clinical application.