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Orthostatic blood pressure (BP) dysregulation can impair cerebral blood perfusion and cognition. Water intake prevents syncope caused by orthostatic hypotension (OHypo) and improves orthostatic tolerance. However, research on scheduled water intake's effect on the association between OHypo and cognition is limited. This study aimed to investigate the impact of scheduled water intake on orthostatic BP dysregulation and mild cognitive impairment (MCI). This cross-sectional study was conducted in rural Fuxin, Liaoning Province, China, using cohort data. Water intake patterns were self-reported, and orthostatic BP was measured. MCI was assessed with the Chinese version of the Montreal Cognitive Assessment-Basic (MoCA-BC).Latent class mixed models were applied to identify systolic BP trajectory patterns. Logistic regression was used to examine the association between orthostatic BP abnormality and MCI, adjusting for potential confounders and including an interaction term for orthostatic BP abnormality and water intake regularity. Linear regression was used to analyze the relationship between orthostatic BP abnormality and total MoCA-BC score. Subgroup analyses were conducted based on age and water intake regularity. The study included 1576 participants: 1236 (78.4%) had normal recovery, 234 (14.8%) had delayed recovery, 36 (2.3%) had OHypo, and 70 (4.5%) had orthostatic hypertension. The average age was 63.2 ± 7.7 years, with a daily water intake of 1612.5 ± 978.8 ml; 1055 (66.9%) were female. Unscheduled water intake significantly interacted with OHypo on MCI (OR 5.82; 95% CI 1.17-35.34; P = 0.039). After adjusting for confounders, scheduled water intake was associated with a lower OR of MCI in those with OHypo (OR 0.11; 95% CI 0.02-0.44; P = 0.003), while unscheduled water intake showed no significant association (OR 0.99; 95% CI 0.41-2.57; P = 0.985). Scheduled water intake is linked to a lower risk of MCI in individuals with OHypo, suggesting a protective role. Promoting scheduled water intake might be inversely associated with MCI in OHypo patients. Further longitudinal studies are needed to confirm these findings and understand the mechanisms involved.
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http://dx.doi.org/10.1038/s41598-025-94818-0 | DOI Listing |
Cell Commun Signal
September 2025
Department of Cytology, Institute of Anatomy, Medical Faculty, Ruhr-University Bochum, Universitätsstr. 150, Building MA 5/52, Bochum, 44801, Germany.
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Mol Psychiatry
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Section on Clinical Genomics and Experimental Therapeutics, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, USA.
Pharmacological modulation of glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) through dual GIP/GLP-1 receptor agonists, commonly used for diabetes and obesity, shows promise in reducing alcohol consumption. We applied drug-target Mendelian randomization (MR) using genetic variation at these loci to assess their long-term effects on problematic alcohol use (PAU), binge drinking, alcohol misuse classifications, liver health, and other substance use behaviors. Genetic proxies for lowered BMI, modeling the appetite-suppressing and weight-reducing effects of variants in both the GIPR and GLP1R loci ("GIPR/GLP1R"), were linked with reduced binge drinking in the primary (β = -0.
View Article and Find Full Text PDFAlcohol Clin Exp Res (Hoboken)
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Research Unit of Psychiatry, Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Background: Alcohol use disorder (AUD) among older adults, particularly with respect to gender differences in treatment outcomes, remains underexplored. Our objective was to explore gender differences in AUD treatment outcomes among older adults, focusing on continuous measures (e.g.
View Article and Find Full Text PDFMethods Cell Biol
September 2025
LR18ES03 Laboratory of Neurophysiology, Cellular Physiopathology and Valorisation of Biomolecules, Faculty of Science of Tunis, University Tunis El Manar, Tunis, Tunisia. Electronic address:
Binge drinking (BD) is a widespread pattern of excessive alcohol consumption among adolescents and young adults with detrimental consequences for brain development. Animal models are essential for investigating the neurobiological mechanisms underlying BD, but selecting an appropriate model is critical to ensure relevance to human behavior. This study aims to validate a murine model of (BD) using Swiss Webster mice.
View Article and Find Full Text PDFJ Safety Res
September 2025
MAIC/UniSC Road Safety Research Collaboration, University of the Sunshine Coast, 90 Sippy Downs Dr, Sippy Downs, Queensland 4556, Australia.
Introduction: Drink driving is a dangerous behavior associated with significant road trauma. The ability to estimate one's alcohol plays an important role in the decision to drink and drive. This systematic review aimed to synthesize the evidence regarding what factors are associated with the accuracy of self-estimated blood and breath alcohol concentrations (BAC/BrAC) and discuss relevant implications for drink driving.
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