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Background And Objectives: Previous studies addressing the association between multiple sclerosis (MS) and stroke yielded conflicting results. The current study aimed to evaluate the association between MS and incident stroke, overall and by main stroke subtypes.
Methods: We conducted a population-based retrospective cohort study utilizing the Clalit Health Services database, the largest healthcare provider in Israel. The cohort included all incident MS patients aged ≥25 years diagnosed between 1 January 2005 and 31 December 2022. Each MS patient was matched to 10 non-MS controls based on age, sex, and population sector. MS cases (exposed group) and non-MS cases (unexposed group) were followed from the index date until 31 December 2023 for stroke occurrence.
Results: The study included 1602 MS patients and 16,020 non-MS controls. Overall stroke was diagnosed in 26 patients in the MS group and 233 in the non-MS group, reflecting a crude incidence rate of 1.61 and 1.40 per 1000 person-years, respectively. The adjusted hazard ratios (HRs) were 0.95 (95 % CI, 0.61-1.48) for overall stroke, 0.94 (95 % CI, 0.59-1.51) for ischemic stroke, and 0.94 (95 % CI, 0.25-3.56) for intracerebral hemorrhage. The results remained consistent when analysis was restricted to patients without a prior history of stroke, when follow-up was restricted to 2 years, and when the cohort was extended to include preexisting MS cases. Age and sex did not modify the association between MS and stroke risk (p-for interaction=0.161 and 0.647, respectively).
Conclusions: Our findings suggest that MS is not associated with an increased risk of stroke.
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http://dx.doi.org/10.1016/j.msard.2025.106715 | DOI Listing |
JPEN J Parenter Enteral Nutr
September 2025
Center for Sarcopenia and Malnutrition Research, Kumamoto Rehabilitation Hospital, Kumamoto, Japan.
Background: Limited evidence exists regarding the cognitive and physical improvement effects of medium-chain triglyceride (MCT) intake in patients with stroke. This study aimed to investigate the association between MCT-enhanced rice consumption and enhancements in outcomes, including cognitive level, in patients following stroke.
Methods: We performed a retrospective cohort study on adults admitted to a rehabilitation center with cognitive decline following acute stroke.
BMC Emerg Med
September 2025
Department of Neurology and Clinical Neuroscience, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany.
Background: Identifying suspected anterior circulation large-vessel occlusion (aLVO) strokes during emergency calls could enhance dispatch efficiency, particularly in rural areas. However, data on emergency medical dispatchers' (EMDs) ability to recognize aLVO symptoms remain limited. This simulation study aimed to evaluate the feasibility of identifying side-specific arm paresis, side-specific conjugate eye deviation (CED), and aphasia during emergency calls by instructing layperson callers to perform brief, standardized examination steps.
View Article and Find Full Text PDFLab Anim Res
September 2025
Department of Pathology, Faculty of Medicine, Kindai University, 377-2 Ohno-Higashi, Osaka-Sayama, Osaka, 589-8511, Japan.
Background: Stroke-prone spontaneously hypertensive rats (SHRSP) exhibit slow-twitch muscle-specific hypotrophy compared with normotensive Wistar-Kyoto rats (WKY). Because slow-twitch muscles are prone to disuse atrophy, SHRSP may experience both disuse atrophy and impaired recovery from it. This study investigated the response of SHRSP to disuse atrophy and subsequent recovery, using WKY as a control.
View Article and Find Full Text PDFClin Genet
September 2025
Department of Pediatrics, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
LONP1 encodes a mitochondrial protease essential for protein quality control and metabolism. Variants in LONP1 are associated with a diverse and expanding spectrum of disorders, including Cerebral, Ocular, Dental, Auricular, and Skeletal anomalies syndrome (CODAS), congenital diaphragmatic hernia (CDH), and neurodevelopmental disorders (NDD), with some individuals exhibiting features of mitochondrial encephalopathy. We report 16 novel LONP1 variants identified in 16 individuals (11 with NDD, 5 with CDH), further expanding the clinical spectrum.
View Article and Find Full Text PDFMol Psychiatry
September 2025
Center for Gene Regulation in Health and Disease, Cleveland State University, Cleveland, OH, 44115, USA.
Dysregulated spine morphology is a common feature in the pathology of many neurodevelopmental and neuropsychiatric disorders. Overabundant immature dendritic spines in the hippocampus are causally related to cognitive deficits of Fragile X syndrome (FXS), the most common form of heritable intellectual disability. Recent findings from us and others indicate autophagy plays important roles in synaptic stability and morphology, and autophagy is downregulated in FXS neurons.
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