PP343 - DETERMINATION OF INSULIN RESISTANCE IN ICU, A PHYSIOLOGICAL CLINICAL STUDY, THE DIRICU STUDY
PP343
DETERMINATION OF INSULIN RESISTANCE IN ICU, A PHYSIOLOGICAL CLINICAL STUDY, THE DIRICU STUDY
C. Dupuis1,*, V. Alves de Araújo2, C. Annicchiarico3, G. Macedo3, C. Pinto Teixeira3, V. Uyttendaele4, T. Desaive4, F. Taccone3, C. Miriam5, T. Carton5, M. Seret4, J.-C. Preiser2
1Intensive care medicine, Clermont Ferrand University hospital, Clermont Ferrand, France, 2intensive care, 3Intensive care medicine, Hopital Universitaire libre de Bruxelles, Bruxelles, 4Université de Liège, Liège, 5Hopital Universitaire libre de Bruxelles, Bruxelles, Belgium
Rationale: Insulin resistance (IR) is a key feature of critical illness, with dynamic changes across metabolic phases. However, its bedside assessment remains challenging. Continuous glucose monitoring (CGM)–derived metrics may offer a pragmatic alternative, but their validity as surrogates of intrinsic insulin sensitivity (SI) is unclear. This study aimed to evaluate CGM-derived indices against SI measured by intravenous glucose tolerance testing (SI_IVGTT).
Methods: In this prospective single-center physiological study, 20 non-diabetic ICU patients with stress hyperglycemia were included within 48 hours of admission. CGM (Dexcom G7) was initiated, and IVGTT was performed on days 2 and 4. SI_IVGTT was estimated using the minimal model. CGM-derived indices (CGM-KG, CGM-T50, CGM-AUC0–180), HOMA-IR, and SI derived from the Intensive Control Insulin-Nutrition-Glucose model (ICING) (SI_ICING) were compared with SI_IVGTT.
Results: No significant correlation was observed between CGM-KG and SI_IVGTT at day 2 (ρ=0.07, p=0.76). At day 4, moderate associations emerged (ρ=0.59, p=0.016) but were not significant after correction (FDR-adjusted p=0.069). CGM-derived indices overall showed limited performance. In contrast, SI_ICING showed the strongest association with SI_IVGTT at day 4 (ρ=0.64, p<0.001, FDR-adjusted p=0.048), with good discrimination (AUC 0.87). HOMA-IR was not informative. CGM indices were more relevant in patients without insulin therapy.
Conclusion: CGM-derived metrics do not reliably reflect intrinsic insulin sensitivity in ICU patients, especially under insulin therapy. Treatment-integrated indices such as SI_ICING may better capture metabolic responsiveness. Further studies are needed to improve metabolic monitoring strategies in critical illness.
Disclosure of Interest: C. Dupuis Other: Dexcom supplied the CGM devices but had no role in the study design, data collection, analysis, or manuscript preparation., V. Alves de Araújo: None declared, C. Annicchiarico: None declared, G. Macedo: None declared, C. Pinto Teixeira: None declared, V. Uyttendaele: None declared, T. Desaive: None declared, F. Taccone: None declared, C. Miriam: None declared, T. Carton: None declared, M. Seret: None declared, J.-C. Preiser: None declared