AI Article Synopsis

  • The study compared BOLD responses in patients with psychophysiological insomnia (PI) and healthy controls (HCs) during single-task and multitask fMRI.
  • Principal component analysis (PCA) was utilized to identify features for machine learning classification, revealing that PCA features outperformed single-task BOLD responses in distinguishing between PI and HCs.
  • Key brain areas identified included the bilateral inferior frontal gyrus and several others, indicating these regions may play significant roles in PI discrimination.

Article Abstract

We investigated the differential spatial covariance pattern of blood oxygen level-dependent (BOLD) responses to single-task and multitask functional magnetic resonance imaging (fMRI) between patients with psychophysiological insomnia (PI) and healthy controls (HCs), and evaluated features generated by principal component analysis (PCA) for discrimination of PI from HC, compared to features generated from BOLD responses to single-task fMRI using machine learning methods. In 19 patients with PI and 21 HCs, the mean beta value for each region of interest (ROIbval) was calculated with three contrast images (i.e., sleep-related picture, sleep-related sound, and Stroop stimuli). We performed discrimination analysis and compared with features generated from BOLD responses to single-task fMRI. We applied support vector machine analysis with a least absolute shrinkage and selection operator to evaluate five performance metrics: accuracy, recall, precision, specificity, and F2. Principal component features showed the best classification performance in all aspects of metrics compared to BOLD response to single-task fMRI. Bilateral inferior frontal gyrus (orbital), right calcarine cortex, right lingual gyrus, left inferior occipital gyrus, and left inferior temporal gyrus were identified as the most salient areas by feature selection. Our approach showed better performance in discriminating patients with PI from HCs, compared to single-task fMRI.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8087661PMC
http://dx.doi.org/10.1038/s41598-021-88845-wDOI Listing

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