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Randomized Controlled Trial
. 2023 Feb 1;46(2):463-468.
doi: 10.2337/dc22-1622.

Efficacy and Safety of Intermittent Fasting in People With Insulin-Treated Type 2 Diabetes (INTERFAST-2)-A Randomized Controlled Trial

Affiliations
Randomized Controlled Trial

Efficacy and Safety of Intermittent Fasting in People With Insulin-Treated Type 2 Diabetes (INTERFAST-2)-A Randomized Controlled Trial

Anna Obermayer et al. Diabetes Care. .

Abstract

Objective: To investigate the safety and feasibility of 3 nonconsecutive days of intermittent fasting (IF) per week over 12 weeks in participants with insulin-treated type 2 diabetes.

Research design and methods: Forty-six people were randomized to an IF or control group. Dietary counseling and continuous glucose monitoring was provided. Coprimary end points were the change in HbA1c from baseline to 12 weeks and a composite end point (weight reduction ≥2%, insulin dose reduction ≥10%, and HbA1c reduction ≥3 mmol/mol).

Results: The IF group showed a significant HbA1c reduction (-7.3 ± 12.0 mmol/mol) compared with the control group (0.1 ± 6.1 mmol/mol) over 12 weeks (P = 0.012). The coprimary end point was achieved by 8 people in the IF and none in the control group (P < 0.001). No severe hypoglycemia occurred.

Conclusions: IF is a safe and feasible dietary option to ameliorate glycemic control while reducing total daily insulin dose and body weight in insulin-treated people with type 2 diabetes.

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Figures

None
Graphical abstract
Figure 1
Figure 1
Trial flowchart.
Figure 2
Figure 2
Change in HbA1c from baseline to 12 weeks in control and IF group. Data are displayed as mean ± SEM. *P = 0.012.
Figure 3
Figure 3
Coprimary end point; percentage of participants achieving each individual aspect and the combined coprimary end point. *P < 0.05, ***P < 0.001.

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