Time spent in target range assessed by self-monitoring blood glucose associates with glycated hemoglobin in insulin treated patients with diabetes.


Journal

Nutrition, metabolism, and cardiovascular diseases : NMCD
ISSN: 1590-3729
Titre abrégé: Nutr Metab Cardiovasc Dis
Pays: Netherlands
ID NLM: 9111474

Informations de publication

Date de publication:
24 09 2020
Historique:
received: 08 04 2020
revised: 01 06 2020
accepted: 11 06 2020
pubmed: 17 7 2020
medline: 11 11 2020
entrez: 17 7 2020
Statut: ppublish

Résumé

Self-monitoring blood glucose (SMBG) remains a widespread tool to monitor blood glucose. The development of diabetes management systems (DMS) allows SMBG to provide additional information as time spent in target range (TIR). This study evaluates the association between HbA1c and TIR, evaluated through DMS, over 2 months, and 2 weeks. Type 1 (T1D) and Type 2 (T2D) insulin-treated patients with diabetes were enrolled. We used the term PIR (Points in Range) instead of TIR, since SMBG provides point-in-time glucose values rather than a continuous trend over time. PIR was calculated in 2-month and 2-week time ranges before available HbA1c measurement. One-hundred ninety-seven patients with T1D and 36 with T2D were recruited. HbA1c and PIR were inversely associated (2 months: R -0.72, 2 weeks R -0.70; p < 0.0001) in all subjects. The relationship did not change when T1D and T2D patients were analyzed separately. For every 10% change of PIR, there was a change of HbA1c by 0.4%. Our study, for the first time, demonstrates a significant correlation between HbA1c and PIR calculated by DMS. DMS offers additional information useful in disease management of patients with T1D and T2D performing SMBG.

Sections du résumé

BACKGROUND AND AIMS
Self-monitoring blood glucose (SMBG) remains a widespread tool to monitor blood glucose. The development of diabetes management systems (DMS) allows SMBG to provide additional information as time spent in target range (TIR). This study evaluates the association between HbA1c and TIR, evaluated through DMS, over 2 months, and 2 weeks.
METHODS AND RESULTS
Type 1 (T1D) and Type 2 (T2D) insulin-treated patients with diabetes were enrolled. We used the term PIR (Points in Range) instead of TIR, since SMBG provides point-in-time glucose values rather than a continuous trend over time. PIR was calculated in 2-month and 2-week time ranges before available HbA1c measurement. One-hundred ninety-seven patients with T1D and 36 with T2D were recruited. HbA1c and PIR were inversely associated (2 months: R -0.72, 2 weeks R -0.70; p < 0.0001) in all subjects. The relationship did not change when T1D and T2D patients were analyzed separately. For every 10% change of PIR, there was a change of HbA1c by 0.4%.
CONCLUSIONS
Our study, for the first time, demonstrates a significant correlation between HbA1c and PIR calculated by DMS. DMS offers additional information useful in disease management of patients with T1D and T2D performing SMBG.

Identifiants

pubmed: 32669240
pii: S0939-4753(20)30238-6
doi: 10.1016/j.numecd.2020.06.009
pii:
doi:

Substances chimiques

Biomarkers 0
Blood Glucose 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0
Insulin 0
hemoglobin A1c protein, human 0

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1800-1805

Informations de copyright

Copyright © 2020 The Italian Diabetes Society, the Italian Society for the Study of Atherosclerosis, the Italian Society of Human Nutrition and the Department of Clinical Medicine and Surgery, Federico II University. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest None. VB is currently employee of Roche Diabetes Care Austria; she was not involved in the study design, conduct or data analysis but she gave her contribute as expert in Accu-Chek Connect DMS.

Auteurs

Antonio Cutruzzolà (A)

Department of Clinical and Experimental Medicine, University Magna Græcia, Viale Europa, 88100, Catanzaro, Italy. Electronic address: antoniocutruzzola@libero.it.

Concetta Irace (C)

Department of Health Science, University Magna Græcia, Viale Europa, 88100, Catanzaro, Italy. Electronic address: irace@unicz.it.

Martina Parise (M)

Department of Health Science, University Magna Græcia, Viale Europa, 88100, Catanzaro, Italy. Electronic address: parise.martina@gmail.com.

Raffaella Fiorentino (R)

Azienda Ospedaliero-Universitaria Mater Domini, Viale Europa, 88100, Catanzaro, Italy. Electronic address: fiorentinoraffaella@tiscali.it.

Pier Francesco Pio Tripodi (PF)

C.C.P. Policlinico Madonna della Consolazione, Via Cardinale Portanova, 89100, Reggio Calabria, Italy. Electronic address: pierfrancesco.tripodi@medmet.it.

Serena Ungaro (S)

C.C.P. Policlinico Madonna della Consolazione, Via Cardinale Portanova, 89100, Reggio Calabria, Italy.

Valerie Babinsky (V)

Roche Diabetes Care GmbH, Millenium Tower Handelskai, 1200, Vienna, Austria. Electronic address: valerie.babinsky@roche.com.

Agostino Gnasso (A)

Department of Clinical and Experimental Medicine, University Magna Græcia, Viale Europa, 88100, Catanzaro, Italy. Electronic address: gnasso@unicz.it.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH