Cargando…

Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)

OBJECTIVE: To determine the efficacy and safety of liraglutide (a glucagon-like peptide-1 receptor agonist) when added to metformin and rosiglitazone in type 2 diabetes. RESEARCH DESIGN AND METHODS: This 26-week, double-blind, placebo-controlled, parallel-group trial randomized 533 subjects (1:1:1)...

Descripción completa

Detalles Bibliográficos
Autores principales: Zinman, Bernard, Gerich, John, Buse, John B., Lewin, Andrew, Schwartz, Sherwyn, Raskin, Philip, Hale, Paula M., Zdravkovic, Milan, Blonde, Lawrence
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699702/
https://www.ncbi.nlm.nih.gov/pubmed/19289857
http://dx.doi.org/10.2337/dc08-2124
_version_ 1782168519823065088
author Zinman, Bernard
Gerich, John
Buse, John B.
Lewin, Andrew
Schwartz, Sherwyn
Raskin, Philip
Hale, Paula M.
Zdravkovic, Milan
Blonde, Lawrence
author_facet Zinman, Bernard
Gerich, John
Buse, John B.
Lewin, Andrew
Schwartz, Sherwyn
Raskin, Philip
Hale, Paula M.
Zdravkovic, Milan
Blonde, Lawrence
author_sort Zinman, Bernard
collection PubMed
description OBJECTIVE: To determine the efficacy and safety of liraglutide (a glucagon-like peptide-1 receptor agonist) when added to metformin and rosiglitazone in type 2 diabetes. RESEARCH DESIGN AND METHODS: This 26-week, double-blind, placebo-controlled, parallel-group trial randomized 533 subjects (1:1:1) to once-daily liraglutide (1.2 or 1.8 mg) or liraglutide placebo in combination with metformin (1 g twice daily) and rosiglitazone (4 mg twice daily). Subjects had type 2 diabetes, A1C 7–11% (previous oral antidiabetes drug [OAD] monotherapy ≥3 months) or 7–10% (previous OAD combination therapy ≥3 months), and BMI ≤45 kg/m(2). RESULTS: Mean A1C values decreased significantly more in the liraglutide groups versus placebo (mean ± SE −1.5 ± 0.1% for both 1.2 and 1.8 mg liraglutide and −0.5 ± 0.1% for placebo). Fasting plasma glucose decreased by 40, 44, and 8 mg/dl for 1.2 and 1.8 mg and placebo, respectively, and 90-min postprandial glucose decreased by 47, 49, and 14 mg/dl, respectively (P < 0.001 for all liraglutide groups vs. placebo). Dose-dependent weight loss occurred with 1.2 and 1.8 mg liraglutide (1.0 ± 0.3 and 2.0 ± 0.3 kg, respectively) (P < 0.0001) compared with weight gain with placebo (0.6 ± 0.3 kg). Systolic blood pressure decreased by 6.7, 5.6, and 1.1 mmHg with 1.2 and 1.8 mg liraglutide and placebo, respectively. Significant increases in C-peptide and homeostasis model assessment of β-cell function and significant decreases in the proinsulin-to-insulin ratio occurred with liraglutide versus placebo. Minor hypoglycemia occurred more frequently with liraglutide, but there was no major hypoglycemia. Gastrointestinal adverse events were more common with liraglutide, but most occurred early and were transient. CONCLUSIONS: Liraglutide combined with metformin and a thiazolidinedione is a well-tolerated combination therapy for type 2 diabetes, providing significant improvements in glycemic control.
format Text
id pubmed-2699702
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher American Diabetes Association
record_format MEDLINE/PubMed
spelling pubmed-26997022010-07-01 Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD) Zinman, Bernard Gerich, John Buse, John B. Lewin, Andrew Schwartz, Sherwyn Raskin, Philip Hale, Paula M. Zdravkovic, Milan Blonde, Lawrence Diabetes Care Original Research OBJECTIVE: To determine the efficacy and safety of liraglutide (a glucagon-like peptide-1 receptor agonist) when added to metformin and rosiglitazone in type 2 diabetes. RESEARCH DESIGN AND METHODS: This 26-week, double-blind, placebo-controlled, parallel-group trial randomized 533 subjects (1:1:1) to once-daily liraglutide (1.2 or 1.8 mg) or liraglutide placebo in combination with metformin (1 g twice daily) and rosiglitazone (4 mg twice daily). Subjects had type 2 diabetes, A1C 7–11% (previous oral antidiabetes drug [OAD] monotherapy ≥3 months) or 7–10% (previous OAD combination therapy ≥3 months), and BMI ≤45 kg/m(2). RESULTS: Mean A1C values decreased significantly more in the liraglutide groups versus placebo (mean ± SE −1.5 ± 0.1% for both 1.2 and 1.8 mg liraglutide and −0.5 ± 0.1% for placebo). Fasting plasma glucose decreased by 40, 44, and 8 mg/dl for 1.2 and 1.8 mg and placebo, respectively, and 90-min postprandial glucose decreased by 47, 49, and 14 mg/dl, respectively (P < 0.001 for all liraglutide groups vs. placebo). Dose-dependent weight loss occurred with 1.2 and 1.8 mg liraglutide (1.0 ± 0.3 and 2.0 ± 0.3 kg, respectively) (P < 0.0001) compared with weight gain with placebo (0.6 ± 0.3 kg). Systolic blood pressure decreased by 6.7, 5.6, and 1.1 mmHg with 1.2 and 1.8 mg liraglutide and placebo, respectively. Significant increases in C-peptide and homeostasis model assessment of β-cell function and significant decreases in the proinsulin-to-insulin ratio occurred with liraglutide versus placebo. Minor hypoglycemia occurred more frequently with liraglutide, but there was no major hypoglycemia. Gastrointestinal adverse events were more common with liraglutide, but most occurred early and were transient. CONCLUSIONS: Liraglutide combined with metformin and a thiazolidinedione is a well-tolerated combination therapy for type 2 diabetes, providing significant improvements in glycemic control. American Diabetes Association 2009-07 2009-03-16 /pmc/articles/PMC2699702/ /pubmed/19289857 http://dx.doi.org/10.2337/dc08-2124 Text en © 2009 by the American Diabetes Association. https://creativecommons.org/licenses/by-nc-nd/3.0/Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ (https://creativecommons.org/licenses/by-nc-nd/3.0/) for details.
spellingShingle Original Research
Zinman, Bernard
Gerich, John
Buse, John B.
Lewin, Andrew
Schwartz, Sherwyn
Raskin, Philip
Hale, Paula M.
Zdravkovic, Milan
Blonde, Lawrence
Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)
title Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)
title_full Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)
title_fullStr Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)
title_full_unstemmed Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)
title_short Efficacy and Safety of the Human Glucagon-Like Peptide-1 Analog Liraglutide in Combination With Metformin and Thiazolidinedione in Patients With Type 2 Diabetes (LEAD-4 Met+TZD)
title_sort efficacy and safety of the human glucagon-like peptide-1 analog liraglutide in combination with metformin and thiazolidinedione in patients with type 2 diabetes (lead-4 met+tzd)
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699702/
https://www.ncbi.nlm.nih.gov/pubmed/19289857
http://dx.doi.org/10.2337/dc08-2124
work_keys_str_mv AT zinmanbernard efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT gerichjohn efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT busejohnb efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT lewinandrew efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT schwartzsherwyn efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT raskinphilip efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT halepaulam efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT zdravkovicmilan efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT blondelawrence efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd
AT efficacyandsafetyofthehumanglucagonlikepeptide1analogliraglutideincombinationwithmetforminandthiazolidinedioneinpatientswithtype2diabeteslead4mettzd