ECEESPE2025 Poster Presentations Diabetes and Insulin (143 abstracts)
1Endocrine Research Unit, Department of Endocrinology, Odense University Hospital, Odense, Denmark; 2Steno Diabetes Center Odense, Odense University Hospital, Odense, Denmark; 3Department of Clinical Research, Faculty of Health Science, University of Southern Denmark, Odense, Denmark; 4Psychiatry West, Region Zealand, Research Unit for Clinical Psychopharmacology, Slagelse, Denmark; 5Mental Health Services in the Region of Southern Denmark, Child and Adolescent Psychiatry Odense, Odense, Denmark; 6Psychiatric Research Unit, Copenhagen University Hospital Psychiatry Region Zealand, Slagelse, Denmark; 7Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark; 8Næstved, Slagelse og Ringsted Sygehuse, Department of Cardiology and Endocrinology, Slagelse, Denmark; 9IRS - Department of Regional Health Research, Faculty of Health Science, University of Southern Denmark, Odense, Denmark; 10Unit of Mental Health Research, Southwest Denmark, Department of Regional Health Services, University of Southern Denmark, Odense, Denmark; 11Mental Health Services in the Region of Southern Denmark, Department of Psychiatry Odense-Svendborg, Svendborg, Denmark; 12OUH, OPEN - Open Patient data Explorative Network, Odense, Denmark
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Background: Individuals with schizophrenia face a 10 to 20-year reduction in life expectancy, primarily due to cardiovascular disease (CVD) and obesity-related type 2 diabetes (T2D). These risks may be exacerbated by treatment with second-generation antipsychotics (SGAs), which may cause obesity and thereby diminish quality of life (QoL). Semaglutide, a GLP-1 receptor agonist approved for obesity has demonstrated significant efficacy in promoting weight loss, and reducing the prevalence of T2D and risks for CVD. Therefore, this trial evaluated whether once-weekly semaglutide improves HbA1c, reduces weight, and enhances mental health and QoL in prediabetic, overweight/obese SGA-treated patients with schizophrenia.
Methods: We conducted a double-blind, randomized, placebo-controlled trial involving 154 adults, aged 18-60 years, with BMI ≥27 kg/m2, SGA-treated schizophrenia, and prediabetes (HbA1c: 3947 mmol/mol). Participants were randomized (1:1) to receive once-weekly semaglutide or placebo, titrated to 1. 0 mg or maximally tolerated dose, over 30 weeks.
Outcomes: In total, 151 participants completed randomization (semaglutide group: 74; placebo group: 77). Intention-to-treat analysis demonstrated that semaglutide reduced HbA1c by 5. 07 mmol/mol (95% CI: -6. 05 to 4. 09) and body weight by 9. 21 kg (95% CI: -11. 68 to -6. 75) compared to placebo. Furthermore, 81% in the semaglutide group vs. 19% in the placebo group obtained an HbA1c <39 mmol/mol (P < 0. 001). The semaglutide group improved physical QoL scores (SF-36) by 3. 6 points (95% CI: 1. 4 to 5. 8), but changed neither mental QoL scores nor psychiatric symptoms outcomes. Finally, the semaglutide group had higher incidence of gastrointestinal symptoms, but experienced no worsening in somatic or mental serious adverse events.
Interpretation: Semaglutide appears safe as adjunct therapy for SGA-treated patients with schizophrenia, prediabetes, and overweight/obesity. During 30 weeks, semaglutide significantly improved glycemic control, promoted weight loss, and enhanced physical QoL without adversely affecting mental health. These findings highlight its potential role in mitigating cardiometabolic risks in this high-risk population.