Association between bipolar disorder and diabetic ketoacidosis/hyperosmolar hyperglycemic state

• Published in: Scientific reports Vol. 15; no. 1; pp. 22701 - 10
• Main Authors: Liu, Han-Jung, Lo, Shih-Chang, Huang, Chien-Ning, Yang, Yi-Sun, Wang, Yu-Hsun, Kornelius, Edy
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 02.07.2025; Nature Portfolio
• Subjects: 692/308; 692/699/2743; Adult; Aged; Bipolar; Bipolar Disorder - complications; Bipolar Disorder - epidemiology; Diabetes; Diabetes Mellitus, Type 2 - complications; Diabetes Mellitus, Type 2 - epidemiology; Diabetic Ketoacidosis - complications; Diabetic Ketoacidosis - epidemiology; Diabetic Ketoacidosis - etiology; DKA; Female; HHS; Humanities and Social Sciences; Humans; Hyperglycemia; Hyperglycemic Hyperosmolar Nonketotic Coma - epidemiology; Incidence; Male; Middle Aged; multidisciplinary; Retrospective Studies; Risk Factors; Science; Science (multidisciplinary); Bipolar; HHS; Diabetes; DKA
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-025-08087-y

Individuals with bipolar disorder have a higher prevalence of type 2 diabetes mellitus (T2DM) and are at increased risk for diabetes-related complications. However, little is known about the association between bipolar disorder and acute hyperglycemic crises, including diabetic ketoacidosis (DKA) and hyperosmolar hyperglycemic state (HHS). This study aimed to evaluate whether bipolar disorder is associated with an increased risk of DKA and HHS in individuals with newly diagnosed T2DM. We conducted a retrospective cohort study using the TriNetX electronic health records network. Adults diagnosed with T2DM between 2016 and 2024 who received at least one glucose-lowering medication were included. Patients with a recorded diagnosis of bipolar disorder within one year before T2DM onset formed the exposure group, while those without bipolar disorder served as controls. Individuals with pre-existing hyperglycemic crises were excluded. Propensity score matching (1:1) was applied to balance demographic factors, body mass index, comorbidities, and medication use. The primary outcome was the incidence of DKA or HHS, analyzed using Cox proportional hazards models to estimate hazard ratios (HRs) with 95% confidence intervals (CIs). After matching ( N  = 39,676 per group), patients with bipolar disorder had a significantly higher risk of hyperglycemic crises (HR 1.65, 95% CI 1.45–1.88). Separate analyses revealed an increased risk of DKA (HR 1.58, 95% CI 1.37–1.82) and HHS (HR 1.95, 95% CI 1.30–2.94). Subgroup analyses suggested that the association was more pronounced in younger patients, White individuals, those with cerebrovascular disease, and those on insulin therapy. Bipolar disorder may be associated with a higher risk of acute hyperglycemic crises in patients with newly diagnosed T2DM. These findings highlight the need for integrated psychiatric and diabetes care to mitigate metabolic decompensation. Future prospective studies are warranted to further explore the mechanisms underlying this association and to develop targeted interventions.