P892 - INCREASED CARBOHYDRATE INTAKE DOES NOT ALTER INSULIN RESISTANCE IN TYPE 2 DIABETIC PATIENTS

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P892

INCREASED CARBOHYDRATE INTAKE DOES NOT ALTER INSULIN RESISTANCE IN TYPE 2 DIABETIC PATIENTS

O. Sobotka1,2,*, M. Ticha2,3, P. Skorepa1,2,4, J. Dusbabova1, L. Sobotka1,2

13rd Department of Internal Medicine-Metabolism and Gerontology, University Hospital Hradec Kralove, 23rd Department of Internal Medicine-Metabolism and Gerontology, Faculty of Medicine in Hradec Kralove, Charles University, Hradec Kralove, 3Department of Internal Medicine, Pardubice Hospital, Pardubice, 4Department of Military Internal Medicine and Military Hygiene, University of Defence, Military Faculty of Medicine, Hradec Kralove, Czech Republic

 

Rationale: Carbohydrate (CHO) intake has long been considered a major contributor to insulin resistance (IR), prompting recommendations for reduced CHO in managing type 2 diabetes. However, previous findings from our group showed that increased CHO intake did not worsen IR in a small diabetic cohort. To validate these preliminary observations, this study included a larger sample to further assess the effects of elevated CHO intake on IR.

Methods: Fifteen patients with type 2 diabetes participated. During the first week, they received a standard diabetic diet with 250 g of CHO daily. In the second week, 150 g of maltodextrin was added daily, split across three meals. Plasma glucose was continuously monitored. At the end of each dietary phase, a 100 g CHO test meal was administered, and plasma glucose, insulin, and C-peptide levels were measured.

Results: Adding maltodextrin did not significantly affect glucose tolerance. The plasma glucose AUC after the CHO test meal remained nearly unchanged: 48.6 h·mmol/L (43.4–60.4) vs. 48.6 h·mmol/L (44.0–60.7). Insulin and C-peptide responses showed modest, non-significant declines: insulin AUC from 179.6 h·U/L (79.2–543.3) to 135.4 h·U/L (87.3–451.1), and C-peptide AUC from 11.0 h·nmol/L (4.6–13.0) to 9.5 h·nmol/L (6.5–12.3).

Conclusion: Our findings support earlier results that short-term increased CHO intake does not worsen IR in type 2 diabetes. These data question the routine restriction of CHO in diabetic nutrition. Given their anabolic role and energy yield, CHO may be a useful component—particularly in hospitalized or recovering patients—without adverse metabolic effects, suggesting a more balanced role in clinical nutrition.

Disclosure of Interest: None declared