Low-carbohydrate diet proved effective and safe for youths with type 1 diabetes: A randomised trial.

Acta Paediatr

Paediatric Endocrine and Diabetes Unit, Edmond and Lily Safra Children's Hospital, Chaim Sheba Medical Centre, Ramat-Gan, Israel.

Published: February 2025

AI Article Synopsis

  • This study aimed to compare the effects of low-carbohydrate (LC) and Mediterranean (MED) diets on glycaemic and metabolic outcomes in adolescents with type 1 diabetes over six months.
  • Both diets led to improvements in blood glucose levels, but the LC diet showed a greater reduction in time spent at high blood sugar levels.
  • Overall, both diets were safe and effective, with no significant increase in hypoglycaemia or cardiovascular risks for participants.

Article Abstract

Aim: Low-carbohydrate (LC) diets have gained popularity. We compared glycaemic and metabolic parameters following an LC versus a Mediterranean (MED) diet in adolescents and youths with type 1 diabetes.

Methods: In a six-month, open-label, randomised trial, 40 individuals were assigned to either diet. Glycaemic outcomes, based on continuous glucose monitoring, included per cent time of blood glucose in the range [3.9-10.0 mmol/L (70-180 mg/dL)] and haemoglobin A1c (HbA1c).

Results: Twenty-eight (70%) were females. The median age was 18 years. After 6 months, the median time in range increased from 47% to 58% in the LC and from 52% to 64% in the MED diet group (p = 0.98). The delta values for the time in range were 16% and 7% for the respective groups (p = 0.09). The percentage of time >13.9 mmol/L (>250 mg/dL) improved more in the LC diet than in the MED diet group: -10% vs. -2% (p = 0.005). The percentage of time <3.0 mmol/L (<54 mg/dL) was comparable. The delta HbA1c improved in both groups: -0.7% vs. -0.1% (p = 0.02). Changes in BMI Z-score and lipid levels were similar.

Conclusion: Both diets improved glycaemic outcomes in adolescents and youths with type 1 diabetes, without increasing hypoglycaemia or cardiovascular risk factors, indicating comparable safety and efficacy.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11706747PMC
http://dx.doi.org/10.1111/apa.17455DOI Listing

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