Ultra Rapid-Acting Inhaled Insulin Improves Glucose Control in Patients With Type 2 Diabetes Mellitus.


Journal

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
ISSN: 1530-891X
Titre abrégé: Endocr Pract
Pays: United States
ID NLM: 9607439

Informations de publication

Date de publication:
May 2021
Historique:
received: 12 07 2020
revised: 12 09 2020
accepted: 15 10 2020
pubmed: 16 4 2021
medline: 4 5 2021
entrez: 15 4 2021
Statut: ppublish

Résumé

To determine whether the use of an inhaled insulin would improve HbA1c. This study was performed in 20 type 2 diabetes mellitus (T2DM) participants with HbA1c values ≥7.5 (58) to ≤11.5% (102 mmol/mol) on a variety of glucose-lowering regimens. Prandial Technosphere insulin (TI) was rapidly titrated based on a treatment algorithm using postprandial blood glucose to calculate premeal doses. A 2-week baseline period was followed by 12 weeks of active treatment with TI. The primary outcome was change in HbA1c. Secondary outcomes included glucose time in range (time in range: 70-180 mg/dL) obtained by a blinded continuous glucose monitoring during the baseline period and at the end of 12 weeks. Goals were to assess how to rapidly and safely initiate TI intensification, determine dosing requirements, and establish an effective dose range in uncontrolled T2DM. Mean HbA1c decreased by -1.6% (-17 mmol/mol) from 9.0% (75 mmol/mol) at baseline to 7.4% (57 mmol/mol) at 12 weeks (P < .0001). Mean time in range increased from 42.2% to 65.7% (P < .0002). Mean prandial doses of TI were 18 or 19 units for all meals. Time below range was 1.1% baseline and 2.6% post treatment (P = .01). Treatment with inhaled TI dosed using a simple algorithm improved glycemic control measured by both HbA1c and time in range, with low rates of hypoglycemia. These data add significantly to understanding TI in the management of T2DM patients for whom prandial insulin is a consideration.

Identifiants

pubmed: 33853718
pii: S1530-891X(20)48362-4
doi: 10.1016/j.eprac.2020.10.004
pii:
doi:

Substances chimiques

Blood Glucose 0
Glycated Hemoglobin A 0
Hypoglycemic Agents 0
Insulin 0
Insulin Glargine 2ZM8CX04RZ

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

449-454

Informations de copyright

Copyright © 2020 AACE. Published by Elsevier Inc. All rights reserved.

Auteurs

Philip Levin (P)

MODEL Clinical Research, Endocrinology, Baltimore, Maryland. Electronic address: pal3420@yahoo.com.

Byron J Hoogwerf (BJ)

Emeritus, Endocrinology, Diabetes and Metabolism, Cleveland Clinic, Cleveland, Ohio; Central Michigan University, Mount Pleasant, Michigan.

Janet Snell-Bergeon (J)

University of Colorado Anschutz Medical Campus, Pediatrics, Aurora, Colorado; Colorado School of Public Health, Department of Biostatistics and Informatics, Aurora, Colorado.

Tim Vigers (T)

University of Colorado Anschutz Medical Campus, Pediatrics, Aurora, Colorado; Colorado School of Public Health, Department of Biostatistics and Informatics, Aurora, Colorado.

Laura Pyle (L)

University of Colorado Anschutz Medical Campus, Pediatrics, Aurora, Colorado; Colorado School of Public Health, Department of Biostatistics and Informatics, Aurora, Colorado.

Lee Bromberger (L)

MODEL Clinical Research, Endocrinology, Baltimore, Maryland.

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Classifications MeSH