Effect of Continuous Glucose Monitoring on Hypoglycemia in Older Adults With Type 1 Diabetes: A Randomized Clinical Trial.


Journal

JAMA
ISSN: 1538-3598
Titre abrégé: JAMA
Pays: United States
ID NLM: 7501160

Informations de publication

Date de publication:
16 06 2020
Historique:
entrez: 17 6 2020
pubmed: 17 6 2020
medline: 2 7 2020
Statut: ppublish

Résumé

Continuous glucose monitoring (CGM) provides real-time assessment of glucose levels and may be beneficial in reducing hypoglycemia in older adults with type 1 diabetes. To determine whether CGM is effective in reducing hypoglycemia compared with standard blood glucose monitoring (BGM) in older adults with type 1 diabetes. Randomized clinical trial conducted at 22 endocrinology practices in the United States among 203 adults at least 60 years of age with type 1 diabetes. Participants were randomly assigned in a 1:1 ratio to use CGM (n = 103) or standard BGM (n = 100). The primary outcome was CGM-measured percentage of time that sensor glucose values were less than 70 mg/dL during 6 months of follow-up. There were 31 prespecified secondary outcomes, including additional CGM metrics for hypoglycemia, hyperglycemia, and glucose control; hemoglobin A1c (HbA1c); and cognition and patient-reported outcomes, with adjustment for multiple comparisons to control for false-discovery rate. Of the 203 participants (median age, 68 [interquartile range {IQR}, 65-71] years; median type 1 diabetes duration, 36 [IQR, 25-48] years; 52% female; 53% insulin pump use; mean HbA1c, 7.5% [SD, 0.9%]), 83% used CGM at least 6 days per week during month 6. Median time with glucose levels less than 70 mg/dL was 5.1% (73 minutes per day) at baseline and 2.7% (39 minutes per day) during follow-up in the CGM group vs 4.7% (68 minutes per day) and 4.9% (70 minutes per day), respectively, in the standard BGM group (adjusted treatment difference, -1.9% (-27 minutes per day); 95% CI, -2.8% to -1.1% [-40 to -16 minutes per day]; P <.001). Of the 31 prespecified secondary end points, there were statistically significant differences for all 9 CGM metrics, 6 of 7 HbA1c outcomes, and none of the 15 cognitive and patient-reported outcomes. Mean HbA1c decreased in the CGM group compared with the standard BGM group (adjusted group difference, -0.3%; 95% CI, -0.4% to -0.1%; P <.001). The most commonly reported adverse events using CGM and standard BGM, respectively, were severe hypoglycemia (1 and 10), fractures (5 and 1), falls (4 and 3), and emergency department visits (6 and 8). Among adults aged 60 years or older with type 1 diabetes, continuous glucose monitoring compared with standard blood glucose monitoring resulted in a small but statistically significant improvement in hypoglycemia over 6 months. Further research is needed to understand the long-term clinical benefit. ClinicalTrials.gov Identifier: NCT03240432.

Identifiants

pubmed: 32543682
pii: 2767159
doi: 10.1001/jama.2020.6928
pmc: PMC7298607
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0

Banques de données

ClinicalTrials.gov
['NCT03240432']

Types de publication

Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2397-2406

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR001422
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK111022
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK020595
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK020541
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001878
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Références

N Engl J Med. 1993 Sep 30;329(14):977-86
pubmed: 8366922
Diabetes Care. 2011 Mar;34(3):586-90
pubmed: 21266651
Diabetes Care. 1995 Apr;18(4):517-22
pubmed: 7497862
JAMA Intern Med. 2014 Jul;174(7):1116-24
pubmed: 24838229
Diabetes Care. 2011 Apr;34(4):795-800
pubmed: 21335621
Diabetes Care. 2017 Apr;40(4):538-545
pubmed: 28209654
J Diabetes Sci Technol. 2017 Nov;11(6):1138-1146
pubmed: 28449590
Diabetes Care. 2014 Feb;37(2):516-20
pubmed: 24041680
JAMA. 2017 Jan 24;317(4):379-387
pubmed: 28118454
Clin Trials. 2005;2(5):379-86
pubmed: 16315646
Diabetes Care. 2010 Dec;33(12):2573-9
pubmed: 21115767
Diabetes Care. 2019 Aug;42(8):1593-1603
pubmed: 31177185
Diabetes Technol Ther. 2010 Apr;12(4):249-55
pubmed: 20210562
J Clin Endocrinol Metab. 2013 Aug;98(8):3411-9
pubmed: 23760624
Diabetes Care. 2016 Apr;39(4):603-10
pubmed: 26681721
J Endocr Soc. 2017 Nov 20;1(12):1445-1460
pubmed: 29344577
Age Ageing. 1997 Sep;26(5):393-400
pubmed: 9351484
Arch Clin Neuropsychol. 2017 Aug 1;32(5):574-584
pubmed: 28419177
Diabetes Care. 2014 Aug;37(8):2114-22
pubmed: 24854041
N Engl J Med. 2008 Oct 2;359(14):1464-76
pubmed: 18779236
Diabetes Technol Ther. 2015 Nov;17(11):773-9
pubmed: 26167948
J Diabetes Sci Technol. 2015 May;9(3):668-75
pubmed: 25591853
Diabetes Care. 2018 Oct;41(10):2155-2161
pubmed: 30089663
JAMA. 2017 Jan 24;317(4):371-378
pubmed: 28118453
Diabetes Technol Ther. 2019 Oct;21(10):602-609
pubmed: 31335193
Diabetes Care. 1987 Sep-Oct;10(5):617-21
pubmed: 3677982

Auteurs

Richard E Pratley (RE)

AdventHealth Translational Research Institute, Orlando, Florida.

Lauren G Kanapka (LG)

Jaeb Center for Health Research, Tampa, Florida.

Michael R Rickels (MR)

Rodebaugh Diabetes Center, University of Pennsylvania Perelman School of Medicine, Philadelphia.

Andrew Ahmann (A)

Oregon Health and Science University, Portland.

Grazia Aleppo (G)

Feinberg School of Medicine, Northwestern University, Chicago, Illinois.

Roy Beck (R)

Jaeb Center for Health Research, Tampa, Florida.

Anuj Bhargava (A)

Iowa Diabetes and Endocrinology Research Center, Des Moines.

Bruce W Bode (BW)

Atlanta Diabetes Associates, Atlanta, Georgia.

Anders Carlson (A)

Park Nicollet International Diabetes Center, Minneapolis, Minnesota.

Naomi S Chaytor (NS)

Elson S. Floyd College of Medicine, Washington State University, Spokane.

D Steven Fox (DS)

University of South California, School of Pharmacy, Los Angeles.

Robin Goland (R)

Naomi Berri Diabetes Center, Columbia University, New York, New York.

Irl B Hirsch (IB)

University of Washington, Seattle.

Davida Kruger (D)

Henry Ford Health System, Detroit, Michigan.

Yogish C Kudva (YC)

Mayo Clinic, Rochester, Minnesota.

Carol Levy (C)

Icahn School of Medicine at Mount Sinai, New York, New York.

Janet B McGill (JB)

Washington University School of Medicine in St Louis, St Louis, Missouri.

Anne Peters (A)

Keck School of Medicine, University of Southern California, Los Angeles.

Louis Philipson (L)

University of Chicago, Chicago, Illinois.

Athena Philis-Tsimikas (A)

Scripps Whittier Diabetes Institute, La Jolla, California.

Rodica Pop-Busui (R)

University of Michigan, Ann Arbor.

Viral N Shah (VN)

Barbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora.

Michael Thompson (M)

University of Massachusetts Medical School, Worcester.

Francesco Vendrame (F)

University of Miami, Miami, Florida.

Alandra Verdejo (A)

Jaeb Center for Health Research, Tampa, Florida.

Ruth S Weinstock (RS)

SUNY Upstate Medical University, Syracuse, New York.

Laura Young (L)

University of North Carolina at Chapel Hill, Chapel Hill.

Kellee M Miller (KM)

Jaeb Center for Health Research, Tampa, Florida.

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