Introduction: The Low Biologically Available Glucose (LoBAG) diet was designed to improve glycemic control of type 2 diabetes mellitus (T2D). This study tested the effectiveness of the diet in free-living participants with T2D.

Methods: A 12-week randomized controlled trial in participants with T2D compared the LoBAG30 diet (30% low starch carbohydrate, 30% protein, 40% fat) to a control diet (55% carbohydrate, 15% protein, 30% fat). Participants were taking metformin at a stable dose or no glucose-lowering medication. Diets were prescribed to be weight neutral and participants were asked to keep physical activity level constant. Diet instruction and dietitian support were provided to both study groups; food was not provided. The primary outcome was hemoglobin A1c (HbA1c) at the end of the intervention, compared between groups.

Results: Forty-eight participants were enrolled (30 female/18 male; 77% white, 15% Black/African American, 2% Asian, 2% American Indian, 4% not reported; 15% Hispanic/Latino). The majority (88%) took metformin. Baseline characteristics were mean (SD) age 57.4 (10.4) years, HbA1c 7.7 (0.6) %, weight 101.5 (19.7) kg, and BMI 35.4 (5.9) kg/m2 with no significant differences between groups. Thirty-eight participants completed the entire intervention; 4/10 non-completers were withdrawn due to the COVID-19 pandemic. HbA1c decreased in both groups over 12 weeks: mean (SD) -1.0 (0.8) % for the LoBAG diet (p<0.01) and -0.6 (0.7) % for control (p<0.01). The final HbA1c was 6.6 (0.6) % in the LoBAG diet group versus 7.2 (0.8) % for control (p=0.01 for comparison between groups). Both groups lost weight: -6.0 (6.9) kg with the LoBAG diet versus -4.3 (3.5) kg for control (p=0.34 for comparison between groups).

Conclusion: Participants with T2D consuming the LoBAG diet had greater reduction in HbA1c over 12 weeks than those consuming a control diet. The LoBAG diet is an effective option for dietary management of blood glucose in patients with T2D.

Disclosure

J. D. Anderson: None. M. A. Hanson: None. L. F. Lysne: None. L. E. Eberly: None. E. R. Seaquist: Consultant; Zucara Therapeutics. D. Knights: None. L. S. Chow: Research Support; Dexcom, Inc. Q. Wang: None. A. Bantle: None.

Funding

University of Minnesota Department of Medicine; National Center for Advancing Translational Sciences (UL1TR002494, KL2TR002492); National Institute of Diabetes and Digestive and Kidney Diseases (K23DK115906)

Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. More information is available at http://www.diabetesjournals.org/content/license.