There is limited work investigating Brain-Computer Interface (BCI) technology in people with Multiple Sclerosis (pwMS), a neurodegenerative disorder of the central nervous system. Present work is limited to recordings at the scalp, which may be significantly altered by changes within the cortex due to volume conduction. The recordings obtained from the sensors, therefore, combine disease-related alterations and task-relevant neural signals, as well as signals from other regions of the brain that are not relevant. The current study aims to unmix signals affected by MS progression and BCI task-relevant signals using estimated source activity to improve classification accuracy. Approach. Data was collected from eight participants with a range of MS severity and ten neurotypical participants. This dataset was used to report the classification accuracy of imagined movements of the hands and feet at the sensor-level and the source-level in the current study. K-means clustering of equivalent current dipoles was conducted to unmix temporally independent signals. The location of these dipoles was compared between MS and control groups and used for classification of imagined movement. Linear discriminant analysis classification was performed at each time-frequency point to highlight differences in frequency band delay. Main Results. Source-level signal acquisition significantly improved decoding accuracy of imagined movement vs. rest and movement vs. movement classification in pwMS and controls. There was no significant difference found in alpha (7-13 Hz) and beta (13-30 Hz) band classification delay between the neurotypical control and MS group, including imagery of limbs with weakness or paralysis. Significance. This study is the first to demonstrate the advantages of source-level analysis for BCI applications in pwMS. The results highlight the potential for enhanced clinical outcomes and emphasize the need for longitudinal studies to assess the impact of MS progression on BCI performance, which is crucial for effective clinical translation of BCI technology. .
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1088/1741-2552/adbec1 | DOI Listing |
Mol Genet Genomic Med
March 2025
Department of Medical Genetics, University of British Columbia (UBC), Vancouver, British Columbia, Canada.
Background: While recently identified heterozygous PRPF8 variants have been linked to various human diseases, their role in neurodevelopmental disorders (NDDs) remains ambiguous. This study investigates the potential association between homozygous PRPF8 variants and NDDs. Most PRPF8 variants are primarily associated with retinal diseases; however, we analyze a family with multiple members diagnosed with NDDs.
View Article and Find Full Text PDFCurr Med Res Opin
March 2025
Merck Healthcare KGaA, Darmstadt, Germany.
Hypothyroidism is a relatively common condition that may affect as many as 10% of the population worldwide when its overt and subclinical presentations are considered. Important clinical comorbidities are highly prevalent in people with hypothyroidism and diminish quality of life and functional status in a manner that is proportional to the number of comorbidities present and their severity. This article reviews the common comorbidities of hypothyroidism, as reported in the literature.
View Article and Find Full Text PDFBackground: this investigation aimed to assess the correlation between the triglyceride glucose (TyG) index and its related indicators, as well as the ratio of triglyceride to high-density lipoprotein cholesterol (TG/HDL-c), with hepatic steatosis and liver fibrosis among middle-aged and elderly participants.
Methods: based on data from the 2017-2020 National Health and Nutrition Examination Survey, the study included adults of ages 40 years and older in the United States. To explore the correlation between TyG and its related indicators, as well as TG/HDL-c with hepatic steatosis and liver fibrosis, multiple regression models were employed.
Background: This study aimed to investigate the clinical value of the serum albumin-to-globulin ratio (AGR) in diagnosing multiple myeloma (MM) and its differential diagnosis from other conditions such as liver and kidney diseases to provide scientific evidence for clinical decision-making.
Methods: A total of 52 newly-diagnosed MM patients from Tongxiang First People's Hospital between January 2020 and June 2024 were selected as the study group. Additionally, 56 patients newly diagnosed with liver disease and 58 patients newly diagnosed with kidney disease during the same period were used as disease control groups, along with 54 healthy individuals serving as the normal control group.
Background: Several particular kinds of typical morphology characteristics of leukemic blasts associated with the specific subtypes of leukemia have been reported. However, B acute lymphoblastic leukemia/lymphoma (B-ALL/LBL) has rarely been reported. The purpose of this study was to investigate the correlation of TCF3::PBX1 fusion with multiple clefts nuclei of blasts in patients with B-ALL/LBL.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!