<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Sun L</submitter><pubmed_abstract>The link between serum glucose-potassium ratio (GPR) and mortality in critically ill toxic encephalopathy (TE) patients is not well defined. This study has aimed to clarify the effect of GPR fluctuations on TE mortality. A total of 3,462 TE patients with TE requiring ICU care were selected from the Medical Information Mart Intensive Care (MIMIC-IV) database. Patients were categorized into three groups based on GPR tertiles: Tertile 1 (n = 1154, range 0.103-1.442), Tertile 2 (n = 1153, range 1.444-1.966), and Tertile 3 (n = 1155, range 1.967-12.937). The primary outcomes studied were 28-day and 90-day all-cause mortality (ACM). To analyze the relationship between GPR and outcomes, we employed Cox regression models adjusted for multiple covariates and restricted cubic splines to explore the potential non-linear association. The 3,462 - patient cohort had a mean age of 67.7 ± 16.6 years, with 58.2% male. The 28-day and 90-day ACM were 21.9% and 31.2%, respectively. Multivariate adjusted analysis showed no overall GPR-ACM correlation at 28 and 90 d. Regarding different groups, with T2 as the reference group (Ref), for 28-day ACM, the adjusted hazard ratio (HR) of the T1 was 1.20 (95% Confidence Interval [CI]: 1.00-1.44, p ≡ P = 0.049), and that of T3 group was 1.22 (95% CI: 1.01-1.47, P = 0.035). For 90 - day ACM, the adjusted HR of the T1 was 1.19 (95% CI: 1.02-1.39, P = 0.023), and the T3 was 1.20 (95% CI: 1.03-1.40). The correlation between the GPR lesvel and ACM was U-shaped association. The left and right - hand side effect sizes at the inflection point (1.65) were 0.472 (HR: 0.472, 95% CI 0.306-0.728, P &lt; 0.001) and 1.127 (HR: 1.127, 95% CI 1.032-1.229, P = 0.0075). Sensitivity analysis was stable. Our findings have revealed a U-shaped relationship between GPR levels and ACM in critically ill patients with TE. Close attention should therefore be paid to this issue in order to improve patient care.</pubmed_abstract><journal>Scientific reports</journal><pagination>26795</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12287516</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>U shaped relationship between serum glucose potassium ratio and mortality in critically ill patients with toxic encephalopathy.</pubmed_title><pmcid>PMC12287516</pmcid><pubmed_authors>Sun L</pubmed_authors><pubmed_authors>Shao F</pubmed_authors><pubmed_authors>Jin P</pubmed_authors><pubmed_authors>Liu T</pubmed_authors></additional><is_claimable>false</is_claimable><name>U shaped relationship between serum glucose potassium ratio and mortality in critically ill patients with toxic encephalopathy.</name><description>The link between serum glucose-potassium ratio (GPR) and mortality in critically ill toxic encephalopathy (TE) patients is not well defined. This study has aimed to clarify the effect of GPR fluctuations on TE mortality. A total of 3,462 TE patients with TE requiring ICU care were selected from the Medical Information Mart Intensive Care (MIMIC-IV) database. Patients were categorized into three groups based on GPR tertiles: Tertile 1 (n = 1154, range 0.103-1.442), Tertile 2 (n = 1153, range 1.444-1.966), and Tertile 3 (n = 1155, range 1.967-12.937). The primary outcomes studied were 28-day and 90-day all-cause mortality (ACM). To analyze the relationship between GPR and outcomes, we employed Cox regression models adjusted for multiple covariates and restricted cubic splines to explore the potential non-linear association. The 3,462 - patient cohort had a mean age of 67.7 ± 16.6 years, with 58.2% male. The 28-day and 90-day ACM were 21.9% and 31.2%, respectively. Multivariate adjusted analysis showed no overall GPR-ACM correlation at 28 and 90 d. Regarding different groups, with T2 as the reference group (Ref), for 28-day ACM, the adjusted hazard ratio (HR) of the T1 was 1.20 (95% Confidence Interval [CI]: 1.00-1.44, p ≡ P = 0.049), and that of T3 group was 1.22 (95% CI: 1.01-1.47, P = 0.035). For 90 - day ACM, the adjusted HR of the T1 was 1.19 (95% CI: 1.02-1.39, P = 0.023), and the T3 was 1.20 (95% CI: 1.03-1.40). The correlation between the GPR lesvel and ACM was U-shaped association. The left and right - hand side effect sizes at the inflection point (1.65) were 0.472 (HR: 0.472, 95% CI 0.306-0.728, P &lt; 0.001) and 1.127 (HR: 1.127, 95% CI 1.032-1.229, P = 0.0075). Sensitivity analysis was stable. Our findings have revealed a U-shaped relationship between GPR levels and ACM in critically ill patients with TE. Close attention should therefore be paid to this issue in order to improve patient care.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Jul</publication><modification>2026-03-17T15:36:39.832Z</modification><creation>2025-08-17T03:06:09.221Z</creation></dates><accession>S-EPMC12287516</accession><cross_references><pubmed>40702256</pubmed><doi>10.1038/s41598-025-12496-4</doi></cross_references></HashMap>