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Background: The research on the impact of dynamic corrected anion gap (cAG) on prognosis is scarce.
Objective: This study aimed to investigate the relationship between changes in cAG (ΔcAG) during intensive care unit (ICU) hospitalization and mortality.
Methods: In this multicenter, retrospective cohort study, patients with both initial and final records of serum sodium, potassium, chloride, bicarbonate, and albumin were recruited from the eICU Collaborative Research Database. Two cohorts were included in the study: cohort A (final cAG > initial cAG) and cohort B (final cAG < initial cAG). Multivariable logistic regression was utilized to assess the association between mortality and ΔcAG in each cohort. ΔcAG was calculated as shown as follows: .
Results: Among the 11,216 enrolled patients, 4,147 (37%) individuals were classified into cohort A, while 7,069 (63%) patients were assigned to cohort B. In cohort A, for every 10% increase in ΔcAG, ICU and hospital mortalities increased by 46.1% (odds ratio: 1.461, 95% confidence interval [1.378, 1.548]) and 55.5% (1.555 [1.467, 1.648]), respectively. Interaction and subgroup analyses demonstrated consistent results among patients with different Acute Physiology and Chronic Health Evaluation Ⅳ (APACHE Ⅳ) scores (≤58 vs. >58), time interval (≤97 h vs. >97 h) and initial cAG (≤16 mEq/L vs. >16 mEq/L). Meanwhile, in cohort B, ICU and hospital mortalities decreased by 31.4% (0.686 [0.619, 0.759]) and 29.4% (0.706 [0.651, 0.764]), respectively, with each 10% increase in ΔcAG, especially among patients with higher APACHE IV scores (>62) and initial cAG (>16 mEq/L). When analyzed categorically, the ΔcAG still exhibited a significant risk gradient across quartiles.
Conclusion: Further elevated cAG after ICU admission demonstrates a robust association with an increased mortality risk in critically ill patients. ICU patients with higher APACHE Ⅳ scores or initial cAG may benefit from measures aimed at reducing cAG.
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http://dx.doi.org/10.3389/fphys.2025.1469985 | DOI Listing |
Zhonghua Nei Ke Za Zhi
September 2025
Department of Neurology of the First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.
To investigate multi-system involvement in Kennedy's disease and its association with disease progression. We retrospectively reviewed the clinical, laboratory, and electrophysiological data from 48 genetically confirmed patients with Kennedy's disease at the Department of Neurology, First Medical Center of the Chinese PLA General Hospital, between February 2016 and February 2024. The disease progression rate was calculated based on the functional scores at baseline and follow-up.
View Article and Find Full Text PDFBMC Neurol
September 2025
Department of Neurology, Asahi General Hospital, 1326 I, Asahi, Chiba 289-2511, Japan.
Background: Spinocerebellar ataxia type 8 (SCA8) is a rare neurodegenerative disease that is caused by CAG/CTG repeat expansion in the overlapping ATXN8 and ATXN8OS genes and basically entails slowly progressive cerebellar dysfunction with resultant dysarthria, limb incoordination, and gait instability. Moreover, patients with SCA8 may also exhibit pyramidal and extrapyramidal signs, cognitive decline, and involuntary movements. Although SCA8 is an autosomal dominant inheritance disorder, it sometimes seems to be sporadic because of reduced penetrance.
View Article and Find Full Text PDFJ Clin Invest
August 2025
Department of Pathology, University of Michigan School of Medicine, Ann Arbor, United States of America.
Degeneration of the neuromuscular system is a characteristic feature of spinal and bulbar muscular atrophy (SBMA), a CAG/polyglutamine (polyQ) expansion disorder caused by mutation in the androgen receptor (AR). Using a gene targeted mouse model of SBMA, AR113Q mice, we demonstrate age-dependent degeneration of the neuromuscular system that initially manifests with muscle weakness and atrophy and progresses to include denervation of neuromuscular junctions and lower motor neuron soma atrophy. Using this model, we tested the hypothesis that therapeutic intervention targeting skeletal muscle during this period of disease progression arrests degeneration of the neuromuscular system.
View Article and Find Full Text PDFFront Immunol
August 2025
Department of Medical Laboratory Diagnostics - Fahrenheit Biobank BBMRI.pl, Medical University of Gdansk, Gdańsk, Poland.
Introduction: Immunonutrition is a part of nutritional interventions in gastrointestinal cancer patients. It seems to be especially important in the preoperative period to reduce, among others, surgery-related complications. The relation between the immune system and gut microbiota has been previously analyzed.
View Article and Find Full Text PDFMicroPubl Biol
July 2025
Geriatric Research Education and Clinical Center, VA Puget Sound Health Care System, Seattle, Washington, United States.
CAG repeat expansions within the HTT gene cause Huntington's disease (HD), a devastating neurodegenerative disease characterized by progressive movement, cognitive, and behavioral symptoms. These expansions result in the expression and accumulation of neurotoxic poly-glutamine (polyQ). Disease initiation depends on the length of the expansion, with fewer than 35 repeats of polyQ typically not pathogenic, while 40 or greater repeats almost always result in HD.
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