Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes. / Mehta, Roopa; Billings, Liana K.; Liebl, Andreas; Vilsbøll, Tina.

I: Diabetic Medicine, Bind 39, Nr. 9, e14901, 2022.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Mehta, R, Billings, LK, Liebl, A & Vilsbøll, T 2022, 'Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes', Diabetic Medicine, bind 39, nr. 9, e14901. https://doi.org/10.1111/dme.14901

APA

Mehta, R., Billings, L. K., Liebl, A., & Vilsbøll, T. (2022). Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes. Diabetic Medicine, 39(9), [e14901]. https://doi.org/10.1111/dme.14901

Vancouver

Mehta R, Billings LK, Liebl A, Vilsbøll T. Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes. Diabetic Medicine. 2022;39(9). e14901. https://doi.org/10.1111/dme.14901

Author

Mehta, Roopa ; Billings, Liana K. ; Liebl, Andreas ; Vilsbøll, Tina. / Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes. I: Diabetic Medicine. 2022 ; Bind 39, Nr. 9.

Bibtex

@article{df251d3bc8724250bb1a5f55c609c569,
title = "Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes",
abstract = "Aims: Two fixed-ratio combinations (FRCs) of basal insulin and glucagon-like peptide-1 receptor agonist (GLP-1RA) are available for once-daily use in adults with type 2 diabetes. We aimed to review the clinical evidence for the efficacy and safety of changing treatment from a basal–bolus insulin (BBI) regimen or a premix insulin to these combination treatments (fixed-ratio or loose) and provide expert opinion on the practicalities of making such a change. Methods: Relevant clinical and trial evidence and general review articles were identified through a literature review of ProQuest (comprising BIOSIS Previews{\textregistered}, Current Contents{\textregistered} Search, Embase{\textregistered} and MEDLINE{\textregistered}) for articles published between 2009 and 2021. Results: We identified nine articles reporting the results of FRCs, and seven articles reporting results of loose combinations of basal insulin and GLP-1RAs, in people who transitioned treatment from BBI or premix regimens. In most trials, combination treatment led to improved or equivalent glycaemic control, and a reduction in body weight or BMI, versus the original regimens. Some trials reported a reduction in total insulin dose. A few trials reported reduced or unchanged hypoglycaemia rates, or increased patient satisfaction, with combination therapy where these endpoints were examined. We provide guidance on transitioning of treatment and the patient types most likely to benefit. Conclusions: In people not achieving glycaemic control with BBI or premix insulin regimens, an FRC or loose combination of basal insulin and GLP-1RA may improve control, decrease the risk of body weight gain or hypoglycaemia and reduce the complexity of treatment.",
keywords = "diabetes mellitus type 2, glucagon-like peptide-1 receptor, IDegLira, insulin, liraglutide, lixisenatide, treatment outcomes",
author = "Roopa Mehta and Billings, {Liana K.} and Andreas Liebl and Tina Vilsb{\o}ll",
note = "Publisher Copyright: {\textcopyright} 2022 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK.",
year = "2022",
doi = "10.1111/dme.14901",
language = "English",
volume = "39",
journal = "Diabetic Medicine",
issn = "0742-3071",
publisher = "Wiley-Blackwell",
number = "9",

}

RIS

TY - JOUR

T1 - Transitioning from basal–bolus or premix insulin therapy to a combination of basal insulin and glucagon-like peptide-1 receptor agonist in people with type 2 diabetes

AU - Mehta, Roopa

AU - Billings, Liana K.

AU - Liebl, Andreas

AU - Vilsbøll, Tina

N1 - Publisher Copyright: © 2022 The Authors. Diabetic Medicine published by John Wiley & Sons Ltd on behalf of Diabetes UK.

PY - 2022

Y1 - 2022

N2 - Aims: Two fixed-ratio combinations (FRCs) of basal insulin and glucagon-like peptide-1 receptor agonist (GLP-1RA) are available for once-daily use in adults with type 2 diabetes. We aimed to review the clinical evidence for the efficacy and safety of changing treatment from a basal–bolus insulin (BBI) regimen or a premix insulin to these combination treatments (fixed-ratio or loose) and provide expert opinion on the practicalities of making such a change. Methods: Relevant clinical and trial evidence and general review articles were identified through a literature review of ProQuest (comprising BIOSIS Previews®, Current Contents® Search, Embase® and MEDLINE®) for articles published between 2009 and 2021. Results: We identified nine articles reporting the results of FRCs, and seven articles reporting results of loose combinations of basal insulin and GLP-1RAs, in people who transitioned treatment from BBI or premix regimens. In most trials, combination treatment led to improved or equivalent glycaemic control, and a reduction in body weight or BMI, versus the original regimens. Some trials reported a reduction in total insulin dose. A few trials reported reduced or unchanged hypoglycaemia rates, or increased patient satisfaction, with combination therapy where these endpoints were examined. We provide guidance on transitioning of treatment and the patient types most likely to benefit. Conclusions: In people not achieving glycaemic control with BBI or premix insulin regimens, an FRC or loose combination of basal insulin and GLP-1RA may improve control, decrease the risk of body weight gain or hypoglycaemia and reduce the complexity of treatment.

AB - Aims: Two fixed-ratio combinations (FRCs) of basal insulin and glucagon-like peptide-1 receptor agonist (GLP-1RA) are available for once-daily use in adults with type 2 diabetes. We aimed to review the clinical evidence for the efficacy and safety of changing treatment from a basal–bolus insulin (BBI) regimen or a premix insulin to these combination treatments (fixed-ratio or loose) and provide expert opinion on the practicalities of making such a change. Methods: Relevant clinical and trial evidence and general review articles were identified through a literature review of ProQuest (comprising BIOSIS Previews®, Current Contents® Search, Embase® and MEDLINE®) for articles published between 2009 and 2021. Results: We identified nine articles reporting the results of FRCs, and seven articles reporting results of loose combinations of basal insulin and GLP-1RAs, in people who transitioned treatment from BBI or premix regimens. In most trials, combination treatment led to improved or equivalent glycaemic control, and a reduction in body weight or BMI, versus the original regimens. Some trials reported a reduction in total insulin dose. A few trials reported reduced or unchanged hypoglycaemia rates, or increased patient satisfaction, with combination therapy where these endpoints were examined. We provide guidance on transitioning of treatment and the patient types most likely to benefit. Conclusions: In people not achieving glycaemic control with BBI or premix insulin regimens, an FRC or loose combination of basal insulin and GLP-1RA may improve control, decrease the risk of body weight gain or hypoglycaemia and reduce the complexity of treatment.

KW - diabetes mellitus type 2

KW - glucagon-like peptide-1 receptor

KW - IDegLira

KW - insulin

KW - liraglutide

KW - lixisenatide

KW - treatment outcomes

U2 - 10.1111/dme.14901

DO - 10.1111/dme.14901

M3 - Review

C2 - 35708737

AN - SCOPUS:85132696783

VL - 39

JO - Diabetic Medicine

JF - Diabetic Medicine

SN - 0742-3071

IS - 9

M1 - e14901

ER -

ID: 321833793