Continuous Glucose Monitoring Profiles in Healthy Nondiabetic Participants: A Multicenter Prospective Study.


Journal

The Journal of clinical endocrinology and metabolism
ISSN: 1945-7197
Titre abrégé: J Clin Endocrinol Metab
Pays: United States
ID NLM: 0375362

Informations de publication

Date de publication:
01 10 2019
Historique:
received: 21 12 2018
accepted: 18 04 2019
pubmed: 28 5 2019
medline: 30 5 2020
entrez: 26 5 2019
Statut: ppublish

Résumé

Use of continuous glucose monitoring (CGM) is increasing for insulin-requiring patients with diabetes. Although data on glycemic profiles of healthy, nondiabetic individuals exist for older sensors, assessment of glycemic metrics with new-generation CGM devices is lacking. To establish reference sensor glucose ranges in healthy, nondiabetic individuals across different age groups using a current generation CGM sensor. Multicenter, prospective study. Twelve centers within the T1D Exchange Clinic Network. Nonpregnant, healthy, nondiabetic children and adults (age ≥6 years) with nonobese body mass index. Each participant wore a blinded Dexcom G6 CGM, with once-daily calibration, for up to 10 days. CGM metrics of mean glucose, hyperglycemia, hypoglycemia, and glycemic variability. A total of 153 participants (age 7 to 80 years) were included in the analyses. Mean average glucose was 98 to 99 mg/dL (5.4 to 5.5 mmol/L) for all age groups except those over 60 years, in whom mean average glucose was 104 mg/dL (5.8 mmol/L). The median time between 70 to 140 mg/dL (3.9 to 7.8 mmol/L) was 96% (interquartile range, 93 to 98). Mean within-individual coefficient of variation was 17 ± 3%. Median time spent with glucose levels >140 mg/dL was 2.1% (30 min/d), and median time spent with glucose levels <70 mg/dL (3.9 mmol/L) was 1.1% (15 min/d). By assessing across age groups in a healthy, nondiabetic population, normative sensor glucose data have been derived and will be useful as a benchmark for future research studies.

Identifiants

pubmed: 31127824
pii: 5479355
doi: 10.1210/jc.2018-02763
pmc: PMC7296129
doi:

Substances chimiques

Blood Glucose 0

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4356-4364

Subventions

Organisme : NIDDK NIH HHS
ID : P30 DK045735
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2019 Endocrine Society.

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Auteurs

Viral N Shah (VN)

Barbara Davis Center for Diabetes, Aurora, Colorado.

Stephanie N DuBose (SN)

Jaeb Center for Health Research, Tampa, Florida.

Zoey Li (Z)

Jaeb Center for Health Research, Tampa, Florida.

Roy W Beck (RW)

Jaeb Center for Health Research, Tampa, Florida.

Anne L Peters (AL)

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

Ruth S Weinstock (RS)

SUNY Upstate Medical University, Syracuse, New York.

Davida Kruger (D)

Henry Ford Medical Center, Detroit, Michigan.

Michael Tansey (M)

University of Iowa, Iowa City, Iowa.

David Sparling (D)

University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.

Stephanie Woerner (S)

Indiana University School of Medicine, Indianapolis, Indiana.

Francesco Vendrame (F)

University of Miami, Miami, Florida.

Richard Bergenstal (R)

International Diabetes Center Park Nicollet, Minneapolis, Minnesota.

William V Tamborlane (WV)

Yale School of Medicine, New Haven, Connecticut.

Sara E Watson (SE)

University of Louisville, Louisville, Kentucky.

Jennifer Sherr (J)

Yale School of Medicine, New Haven, Connecticut.

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