The brain's functional network can be analyzed as a set of distributed functional modules. Previous studies using the static method suggested the modularity of the brain function network decreased due to stroke; however, how the modular network changes after stroke, particularly over time, is far from understood. This study collected resting-state functional MRI data from 15 stroke patients and 15 age-matched healthy controls. The patients exhibit distinct clinical symptoms, presenting in mild (n = 6) and severe (n = 9) subgroups. By using a multilayer network model, a dynamic modular structure was detected and corresponding interaction measurements were calculated. The results demonstrated that the module structure and interaction had changed following the stroke. Importantly, the significant differences in dynamic interaction measures demonstrated that the module interaction alterations were not independent of the initial degree of clinical severity. Mild patients were observed to have a significantly lower between-module interaction than severe patients as well as healthy controls. In contrast, severe patients showed remarkably lower within-module interaction and had a reduced overall interaction compared to healthy controls. These findings contributed to the development of post-stroke dynamics analysis and shed new light on brain network interaction for stroke patients.Clinical relevance- Dynamic module interaction analysis underpins the post-stroke functional plasticity and reorganization, and may enable new insight into rehabilitation strategies to promote recovery of function.
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http://dx.doi.org/10.1109/EMBC40787.2023.10340633 | DOI Listing |
Sci Rep
December 2024
School of Chemistry, Faculty of Engineering and Physical Sciences, University of Southampton, Life Sciences Building 85, University Road, Highfield, Southampton, SO17 1BJ, UK.
Osteoarthritis (OA) is a complex disease of cartilage characterised by joint pain, functional limitation, and reduced quality of life with affected joint movement leading to pain and limited mobility. Current methods to diagnose OA are predominantly limited to X-ray, MRI and invasive joint fluid analysis, all of which lack chemical or molecular specificity and are limited to detection of the disease at later stages. A rapid minimally invasive and non-destructive approach to disease diagnosis is a critical unmet need.
View Article and Find Full Text PDFInt J Bipolar Disord
December 2024
Department for Psychiatry, Psychosomatic Medicine and Psychotherapy, University Hospital Frankfurt-Goethe University, Frankfurt am Main, Germany.
Background: Attention-deficit/hyperactivity disorder (ADHD) is a common neuro-developmental disorder that often persists into adulthood. Moreover, it is frequently accompanied by bipolar disorder (BD) as well as borderline personality disorder (BPD). It is unclear whether these disorders share underlying pathomechanisms, given that all three are characterized by alterations in affective states, either long or short-term.
View Article and Find Full Text PDFEur Arch Psychiatry Clin Neurosci
December 2024
Laboratory of Clinical Neuropathology, Mental Health Research Center, Kashirskoe Shosse 34, 115522, Moscow, Russia.
Previously we found altered microglia-neuron interactions in the prefrontal cortex in schizophrenia. We hypothesized that microglia-neuron interactions may be dysregulated in the caudate nucleus in schizophrenia. A postmortem ultrastructural morphometric study was performed to investigate satellite microglia (SatMg) and adjacent neurons in the head of the caudate nucleus in 21 cases of schizophrenia and 20 healthy controls.
View Article and Find Full Text PDFPatients with cirrhosis have high systemic inflammation (TNFα, CRP, and IL-6) that is associated with poor outcomes. These biomarkers need continuous non-invasive monitoring, which is difficult with blood. We studied the AWARE sweat-sensor to measure these in passively expressed sweat in healthy people (N = 12) and cirrhosis (N = 32, 10 outpatients/22 inpatients) for 3 days.
View Article and Find Full Text PDFSci Rep
December 2024
Department of Clinical Sciences, College of Veterinary Medicine, North Carolina State University, 1060 William Moore Dr, Raleigh, NC, 27607, USA.
Hypertrophic cardiomyopathy (HCM) afflicts humans, cats, pigs, and rhesus macaques. Disease sequelae include congestive heart failure, thromboembolism, and sudden cardiac death (SCD). Sarcomeric mutations explain some human and cat cases, however, the molecular basis in rhesus macaques remains unknown.
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