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Carbohydrate-deficient transferrin (CDT) and the γ-glutamyltransferase-CDT derived Anttila-Index are established biomarkers for sustained heavy alcohol consumption and their potential role to predict delirium and mortality in critically ill patients is not clear. In our prospective observational study, we included 343 consecutive patients admitted to our ICU, assessed the occurrence of delirium and investigated its association with biomarkers of alcohol abuse measured on the day of ICU admission. 35% of patients developed delirium during ICU stay. We found significantly higher CDT levels (p = 0.011) and Anttila-Index (p = 0.001) in patients with delirium. CDT above 1.7% (OR 2.06), CDT per percent increase (OR 1.26, AUROC 0.75), and Anttila-Index per unit increase (OR 1.28, AUROC 0.74) were associated with delirium development in adjusted regression models. Anttila-Index and CDT also correlated with delirium duration exceeding 5 days. Additionally, Anttila-Index above 4, Anttila-Index per unit increase, and CDT per percent increase were independently associated with hospital mortality.
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http://dx.doi.org/10.1016/j.isci.2023.108044 | DOI Listing |
J Affect Disord
September 2025
Département de psychiatrie et d'addictologie, Université de Montréal, Montréal, Québec, Canada; Centre de recherche de l'Institut universitaire en santé mentale (CR-IUSMM), Université de Montréal, Montréal, Québec, Canada.
This study explored the role of metabolic syndrome (MetS) and health-related behaviors in the progression of depressive symptoms over a one-year naturalistic follow-up in patients with depressive disorder. Using data from 153 participants recruited through the Signature Biobank at a psychiatric emergency setting, we tested whether MetS mediated the relationship between health-related behaviors such as smoking, alcohol and drug use, and sleep, and depressive symptom trajectories. Linear mixed models revealed that while depressive symptoms significantly decreased over time, higher MetS score was associated with a slower improvement in depressive symptoms.
View Article and Find Full Text PDFJ Nutr Health Aging
September 2025
Department of Twin Research & Genetic Epidemiology, King's College London, London, United Kingdom; Department of Pathophysiology and Transplantation, Università Degli Studi di Milano, Via Francesco Sforza, 35, 20122 Milan, Italy; Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Angelo Bia
Introduction: The gut-liver axis regulates metabolic homeostasis, with bile acids (BAs) serving as key signalling molecules. BA dysregulation is implicated in metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction- and alcohol-associated liver disease (MetALD), yet consistent identification of BA markers and their mechanistic roles across different stages of these diseases remain elusive.
Methods: We integrated three complementary studies to examine BA dysregulation: a population-based cohort (1522 females from TwinsUK with serum BA and liver biomarker data), a clinical cohort (30 patients with steatotic liver disease, fibrosis stages F0-F4, and 4 controls), and rodent models (20 rats with MASLD/MetALD vs.
Maturitas
August 2025
Navarrabiomed, Hospital Universitario de Navarra (HUN), Universidad Pública de Navarra (UPNA), IdiSNA, Pamplona, Navarra, Spain; CIBER of Frailty and Healthy Aging (CIBERFES), Instituto de Salud Carlos III, Madrid, Spain.
Aim: To examine the association between intrinsic capacity and cancer mortality in middle-aged and older adults.
Methods: We analysed a prospective cohort of 443,130 participants from the UK Biobank, with seven biomarkers reflecting the level of functioning in five domains of intrinsic capacity to calculate an overall score (ranging from 0 [better] to +4 [poor]). Associations between intrinsic capacity scores and mortality from any type of cancer (censored as of December 31, 2022) were estimated using Cox proportional hazard models adjusted for multiple potential confounders.
J Anal Toxicol
September 2025
Department of Laboratory Medicine, Mayo Clinic Arizona, Phoenix, AZ, USA.
Background: Alcohol biomarkers including ethyl glucuronide (EtG) and phosphatidylethanol (PEth) are ordered frequently in clinical and forensic settings including solid organ transplantation. PEth provides a long detection window but can be insensitive to light drinking. In contrast, EtG and ethyl sulfate (EtS) can be elevated after light alcohol consumption and might complement PEth testing.
View Article and Find Full Text PDFPlasma proteomic signatures accurately predict disease risk, but our understanding of the mechanisms contributing to the predictive value of the proteome remains limited. Here, we characterized proteomic biomarkers of 19 age-related diseases, based on observational associations between 2,923 protein levels and incidence of these outcomes in the UK Biobank (N = 45,438). To identify the subset of these biomarkers that may represent causal drivers of disease, we first employed Mendelian Randomization (MR) and found that only 8% of the protein-disease associations with genetic instruments showed suggestive evidence of causal relationships, and were more likely to pertain to only a single disease.
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