Type 1 diabetes

Ketone production and excretion even during mild hyperglycemia and the impact of sodium-glucose co-transporter inhibition in type 1 diabetes

Diabetes Res Clin PractPublished Secondary analysis of a single-arm open-label trial of empagliflozin

Authors' conclusion

Even mild hyperglycemia is associated with greater ketone production, compensated by urinary excretion, in T1D. However, SGLTi exaggerates production and partially reduces compensatory excretion, particularly in women.

Study context

Population
Adults with T1D (50 % female), aged 24 ± 5 years, HbA1c 8.0 ± 0.9 %, T1D duration 17.5 ± 7 years
Participants
40 adults
Comparison
Mild hyperglycemia vs euglycemia, before and after empagliflozin
Methodological details8-week, clamped euglycemia and mild hyperglycemia during extended fasting
  • 8-week
  • Clamped euglycemia and mild hyperglycemia during extended fasting

Primary result

As reported in the abstract

Urine BHB (production) · prior to treatment

P < 0.001

Further findings

%

OutcomeMild hyperglycemiaEuglycemiaP value
BHB fractional excretion0.9 (IQR 0.3–1.6)0.4 (IQR 0.2–0.9)P < 0.001

Effect of SGLTi during mild hyperglycemia · after 8 weeks of empagliflozin

Beta-hydroxybutyrate (BHB) fractional excretion decreased to (p < 0.001)
0.3 %
Plasma BHB increased to (p < 0.001)
0.21 [0.05-0.40] mmol/L
SGLTi increased BHB production
Effect particularly in females (interaction p < 0.001)

Original publication

Ketone production and excretion even during mild hyperglycemia and the impact of sodium-glucose co-transporter inhibition in type 1 diabetes. Diabetes Res Clin Pract. Published 28 November 2023. doi:10.1016/j.diabres.2023.111031

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