Objective: Corpus callosum (CC) damage is the most consistent and typical change in early Parkinson's disease (PD), and is associated with various PD symptoms. However, the precise relationship between CC subregions and specific PD symptoms have not been identified comprehensively. In this study, we investigated the association between specific CC subregion alterations and PD symptoms using diffusion-weighted imaging.

Methods: 70 PD patients in early-stage from the Parkinson's Progression Markers Initiative cohort were included. Fixel-based analysis (FBA) was used to calculate mean values of fiber density (FD), fiber cross-section (FC), and combined measure of FD and FC (FDC) for 7 CC subregions. Regression analyses between FBA metrics and PD symptom scores were performed to evaluate associations between CC subregion metrics and clinical symptom scores. Diffusion tensor imaging (DTI) metrics were also analyzed.

Results: The score of akinetic rigid symptoms was negatively associated with FDC value of CC rostral body. The score of Activities of Daily Living was positively associated with FD value of CC anterior midbody. The score of gastrointestinal dysfunction was negatively associated with FDC value of CC rostrum. The severity of thermoregulatory dysfunction and cognitive decline was accompanied by an improvement in FBA metrics for several CC subregions. No significant associations were found using DTI metrics.

Conclusions: In early-stage of PD, motor, autonomic, and cognitive functions are associated with specific subregions of CC, and compensatory changes in CC may exist to maintain normal autonomic and cognitive functions.

Download full-text PDF

Source
http://dx.doi.org/10.1007/s10072-024-07951-5DOI Listing

Publication Analysis

Top Keywords

corpus callosum
8
associated symptoms
8
early-stage parkinson's
8
parkinson's disease
8
fba metrics
8
symptom scores
8
negatively associated
8
associated fdc
8
autonomic cognitive
8
cognitive functions
8

Similar Publications

Background: Studies on the impact of white matter hyperintensity (WMH) on function outcome have primarily concentrated on WMH volume, overlooking the potential significance of WMH location. This study aimed to investigate the relationship between WMH location and outcome in patients with their first-ever acute ischemic stroke (AIS).

Methods: Patients who underwent their first AIS between September 2021 and September 2022 were recruited.

View Article and Find Full Text PDF

Background: Age, sex, and APOE genotype are well-established risk factors for late-onset Alzheimer's Disease (LOAD). Previous findings demonstrate that neuroinflammatory profiles of the human midlife female brain closely resemble the human AD brain. Given APOE's role in LOAD pathogenesis, here we investigate the contribution of this risk factor on targeted AD relevant transcriptional pathways.

View Article and Find Full Text PDF

Background: Inflammation plays a pivotal role in driving the development and progression of Alzheimer's disease (AD) in the human brain, offering a promising avenue for therapeutic intervention. However, the initiation phase of inflammation and its potential sex differences remain elusive. In this study, we aim to provide translational validity to our preclinical findings by testing two hypotheses: 1) the inflammatory profile of late-onset AD (LOAD) is initiated and detectable during midlife aging, and 2) sex differences manifest in the brain by midlife.

View Article and Find Full Text PDF

Background: Our studies show that the small non-coding RNA, mir20a-3p, is neuroprotective for stroke in the acute phase and also attenuates long term cognitive decline in middle-aged female rats. Cognitive decline due to vascular diseases, such as stroke, is associated with secondary neurodegeneration in cortex and limbic structures. In this study, we assessed the volume of white matter, ventricles and regional diffusion-weighted MR imaging measures to delineate pathological tissue characteristics from the postmortem brain of stroke rats.

View Article and Find Full Text PDF

Cuprizone (CPZ) is a widely used toxin that induces demyelinating diseases in animal models, producing multiple sclerosis (MS)-like pathology in rodents. CPZ is one of the few toxins that triggers demyelination and subsequent remyelination following the cessation of its application. This study examines the functional consequences of CPZ-induced demyelination and the subsequent recovery of neural communication within the anterior cingulate cortex (ACC), with a particular focus on inter-hemispheric connectivity via the corpus callosum.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!