Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists

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Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists. / Kielgast, Urd; Holst, Jens Juul; Madsbad, Sten.

In: Current Diabetes Reviews, Vol. 5, No. 4, 11.2009, p. 266-75.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Kielgast, U, Holst, JJ & Madsbad, S 2009, 'Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists', Current Diabetes Reviews, vol. 5, no. 4, pp. 266-75.

APA

Kielgast, U., Holst, J. J., & Madsbad, S. (2009). Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists. Current Diabetes Reviews, 5(4), 266-75.

Vancouver

Kielgast U, Holst JJ, Madsbad S. Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists. Current Diabetes Reviews. 2009 Nov;5(4):266-75.

Author

Kielgast, Urd ; Holst, Jens Juul ; Madsbad, Sten. / Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists. In: Current Diabetes Reviews. 2009 ; Vol. 5, No. 4. pp. 266-75.

Bibtex

@article{0643a26ce4034ed5adfd54c13ed5346e,
title = "Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists",
abstract = "GLP-1 (glucagon-like peptide-1) is a peptide hormone secreted from endocrine cells in the intestinal mucosa in response to meals. The major effects of GLP-1 are to increase glucose-induced insulin secretion and reduce glucagon release, but GLP-1 also inhibits gastric emptying rate and reduces appetite and bodyweight in obese subjects. In vivo studies using animal models of type 2 diabetes and in vitro studies using human islet cells have suggested that GLP-1 or GLP-1 analogues are also able to increase beta-cell mass, but in animal models of type 1 diabetes, there is much less evidence for a beta-cell preserving effect. This review summarizes the present knowledge of GLP-1 and its analogues regarding its role as a possible treatment in patients with type 1 diabetes. The studies that address the effect of GLP-1 and GLP-1 analogues on beta-cell mass in both type 2 and type 1 diabetes, as well as the potential of GLP-1 as an adjuvant therapy in islet cell transplantation, will be reviewed. Suggestions for future studies of GLP-1 treatment in type 1 diabetes may include early treatment in order to preserve beta-cell mass and prolong the remission period, but should also take a potential insulin sparing effect and changes in the risk of hypoglycemia into account.",
keywords = "Animals, Diabetes Mellitus, Type 1, Glucagon-Like Peptide 1, Humans, Hypoglycemic Agents, Peptides, Receptors, Glucagon, Venoms",
author = "Urd Kielgast and Holst, {Jens Juul} and Sten Madsbad",
year = "2009",
month = nov,
language = "English",
volume = "5",
pages = "266--75",
journal = "Current Diabetes Reviews (Online)",
issn = "1875-6417",
publisher = "Bentham Science Publishers",
number = "4",

}

RIS

TY - JOUR

T1 - Treatment of type 1 diabetic patients with glucagon-like peptide-1 (GLP-1) and GLP-1R agonists

AU - Kielgast, Urd

AU - Holst, Jens Juul

AU - Madsbad, Sten

PY - 2009/11

Y1 - 2009/11

N2 - GLP-1 (glucagon-like peptide-1) is a peptide hormone secreted from endocrine cells in the intestinal mucosa in response to meals. The major effects of GLP-1 are to increase glucose-induced insulin secretion and reduce glucagon release, but GLP-1 also inhibits gastric emptying rate and reduces appetite and bodyweight in obese subjects. In vivo studies using animal models of type 2 diabetes and in vitro studies using human islet cells have suggested that GLP-1 or GLP-1 analogues are also able to increase beta-cell mass, but in animal models of type 1 diabetes, there is much less evidence for a beta-cell preserving effect. This review summarizes the present knowledge of GLP-1 and its analogues regarding its role as a possible treatment in patients with type 1 diabetes. The studies that address the effect of GLP-1 and GLP-1 analogues on beta-cell mass in both type 2 and type 1 diabetes, as well as the potential of GLP-1 as an adjuvant therapy in islet cell transplantation, will be reviewed. Suggestions for future studies of GLP-1 treatment in type 1 diabetes may include early treatment in order to preserve beta-cell mass and prolong the remission period, but should also take a potential insulin sparing effect and changes in the risk of hypoglycemia into account.

AB - GLP-1 (glucagon-like peptide-1) is a peptide hormone secreted from endocrine cells in the intestinal mucosa in response to meals. The major effects of GLP-1 are to increase glucose-induced insulin secretion and reduce glucagon release, but GLP-1 also inhibits gastric emptying rate and reduces appetite and bodyweight in obese subjects. In vivo studies using animal models of type 2 diabetes and in vitro studies using human islet cells have suggested that GLP-1 or GLP-1 analogues are also able to increase beta-cell mass, but in animal models of type 1 diabetes, there is much less evidence for a beta-cell preserving effect. This review summarizes the present knowledge of GLP-1 and its analogues regarding its role as a possible treatment in patients with type 1 diabetes. The studies that address the effect of GLP-1 and GLP-1 analogues on beta-cell mass in both type 2 and type 1 diabetes, as well as the potential of GLP-1 as an adjuvant therapy in islet cell transplantation, will be reviewed. Suggestions for future studies of GLP-1 treatment in type 1 diabetes may include early treatment in order to preserve beta-cell mass and prolong the remission period, but should also take a potential insulin sparing effect and changes in the risk of hypoglycemia into account.

KW - Animals

KW - Diabetes Mellitus, Type 1

KW - Glucagon-Like Peptide 1

KW - Humans

KW - Hypoglycemic Agents

KW - Peptides

KW - Receptors, Glucagon

KW - Venoms

M3 - Journal article

C2 - 19925391

VL - 5

SP - 266

EP - 275

JO - Current Diabetes Reviews (Online)

JF - Current Diabetes Reviews (Online)

SN - 1875-6417

IS - 4

ER -

ID: 132048068