Cited by 82Diabetes Management and ResearchDiabetes Treatment and ManagementDiabetes Management and Education

The effect of discontinuing continuous glucose monitoring in adults with type 2 diabetes treated with basal insulin

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Aleppo, Grazia, Beck, Roy W., Bailey, Ryan, Ruedy, Katrina J., Calhoun, Peter, Peters, Anne L., Pop-Busui, Rodica, Philis-Tsimikas, Athena +89 more·2021·Diabetes Care

Published version of a preprint

Abstract

OBJECTIVE: To explore the effect of discontinuing continuous glucose monitoring (CGM) after 8 months of CGM use in adults with type 2 diabetes treated with basal without bolus insulin. RESEARCH DESIGN AND METHODS: This multicenter trial had an initial randomization to either real-time CGM or blood glucose monitoring (BGM) for 8 months followed by 6 months in which the BGM group continued to use BGM (n = 57) and the CGM group was randomly reassigned either to continue CGM (n = 53) or discontinue CGM with resumption of BGM for glucose monitoring (n = 53). RESULTS: In the group that discontinued CGM, mean time in range (TIR) 70–180 mg/dL, which improved from 38% before initiating CGM to 62% after 8 months of CGM, decreased after discontinuing CGM to 50% at 14 months (mean change from 8 to 14 months −12% [95% CI −21% to −3%], P = 0.01). In the group that continued CGM use, little change was found in TIR from 8 to 14 months (baseline 44%, 8 months 56%, 14 months 57%, mean change from 8 to 14 months 1% [95% CI −11% to 12%], P = 0.89). Comparing the two groups at 14 months, the adjusted treatment group difference in mean TIR was −6% (95% CI −16% to 4%, P = 0.20). CONCLUSIONS: In adults with type 2 diabetes treated with basal insulin who had been using real-time CGM for 8 months, discontinuing CGM resulted in a loss of about one-half of the initial gain in TIR that had been achieved during CGM use.

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  • Interruption of access to CGM is associated with worsening outcomes.

    “Interruption of access to CGM is associated with a worsening of outcomes (7,15); therefore, it is important for individuals on CGM to have consistent access to devices.”

    From 7. Diabetes Technology: Standards of Care in Diabetes—2025 (2025) · cites this paper as [15]

  • CGM discontinuation in individuals with type 2 diabetes on basal insulin caused partial reversal of A1C reduction and TIR improvements, suggesting that continued CGM use achieves the greatest benefits.

    “CGM discontinuation in individuals with type 2 diabetes on basal insulin caused partial reversal of A1C reduction and TIR improvements, suggesting that continued CGM use achieves the greatest benefits (15).”

    From 7. Diabetes Technology: Standards of Care in Diabetes—2025 (2025) · cites this paper as [15]

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References 21 · Cited by 82

Authors
Aleppo, G., Beck, R. W., Bailey, R., Ruedy, K. J., Calhoun, P., Peters, A. L., Pop-Busui, R., Philis-Tsimikas, A., Bao, S., Umpierrez, G., Davis, G., Kruger, D., Bhargava, A., Young, L., Buse, J. B., McGill, J. B., Martens, T., Nguyen, Q. T., Orozco, I., Biggs, W., Lucas, K. J., Polonsky, W. H., Price, D., Bergenstal, R. M., MOBILE Study Group, Martens, T., Carlson, A., Bergenstal, R. M., Chambers, S., Yang, S., Young, L., Buse, J., Kirkman, M. S., Kass, A., Fraser, R., Kruger, D., Cushman, T., Davis, G., Ramos, C., Umpierrez, G., Peters, A. L., Magar, M., Walker, M., Serafin-Dokhan, S., McGill, J. B., Salam, M., Hurst, S., Clifton, M. J., Aleppo, G., Kravarusic, J., Bansal, A., Fulkerson, C., Pop-Busui, R., Ang, L., Richardson, C., Mizokami-Stout, K., Reiss, J., Leone, V., Bhargava, A., Stifel, K., Philis-Tsimikas, A., Dailey, G., Change, A., McCallum, J., Garcia, M. I., Bao, S., Davis, D., Lovell, C., Root, C., Biggs, W., Toler, F., Wilhelm, L., Eifert, R., Murguia, L., Cota, B., Nguyen, Q. T., Nguyen, L., Lipski, R., Orozco, I., Lawrence, M. K., Fournier, A., Carter, M., Lucas, K. J., Hoover, S., Beck, R. W., Ruedy, K. J., Calhoun, P., Bailey, R., Cohen, N., Mouse, T., Rusnak, J., Campos, T., Price, D., Njeru, N., Arant, T., Beck, S. E., & Balo, A.
Affiliations
  • University of North Carolina School of Medicine, Chapel Hill, NC
  • Behavioral Diabetes Institute, San Diego, CA
  • Park Nicollet Health Services (US)
  • HealthPartners (US)
  • University of North Carolina at Chapel Hill (US)
  • University of Southern California (US)
  • Washington University in St. Louis (US)
  • Northwestern University (US)
  • University of Michigan (US)
  • Vanderbilt University Medical Center (US)
  • Emory University (US)
  • Carteret General Hospital (US)
  • Jaeb Center for Health Research (US)
  • Dexcom (United States) (US)
Corresponding author
MOBILE Study Group
Venue
Diabetes Care
Published
2021-09-29
Volume
44
Issue
12
Pages
2729-2737
ISSN
  • 0149-5992 (ISSN-L)
  • 1935-5548
OpenAlex
W3204375546
Cited by
82
References
21
Citations by year
2026: 11 · 2025: 21 · 2024: 21 · 2023: 16 · 2022: 13
FWCI
9.33
Type
journal article
Language
en
Open access
Locations
  • Diabetes Care (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Amgen
  • Bristol-Myers Squibb
  • Eli Lilly and Company
  • AstraZeneca
  • Sanofi
  • Intarcia Therapeutics
  • Bigfoot Biomedical
  • Insulet Corporation
  • MannKind Corporation
  • Dexcom
  • Kowa Company
  • Mylan
  • Zafgen
  • Tandem Diabetes Care
  • Nevro
  • Novo Nordisk
  • Roche Diabetes Care
  • National Institutes of Health (UL1TR001422)
  • Abbott Diabetes Care
  • National Institute of Diabetes and Digestive and Kidney Diseases (P30DK092926, P30DK020572, P30DK124723, P30DK111022)
  • National Center for Advancing Translational Sciences
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Treatment and Management
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Education
Keywords
continuous glucose monitoring, type 2 diabetes, basal insulin, time in range, blood glucose monitoring, glycemic control, real-time glucose monitoring
MeSH terms
Adult, Blood Glucose, Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Glycated Hemoglobin, Humans, Hypoglycemic Agents, Insulin, Blood Glucose Self-Monitoring

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