Cargando…
Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study
BACKGROUND: Basal insulin reduces fasting blood glucose levels, but postprandial blood glucose levels may remain higher. Traditional strategies with rapid insulin intensification can cause hypoglycemic episodes and weight gain. Glucagon-like peptide-1 receptor agonists, such as the short-acting lixi...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218842/ https://www.ncbi.nlm.nih.gov/pubmed/30455779 http://dx.doi.org/10.1016/j.curtheres.2018.09.001 |
_version_ | 1783368535013064704 |
---|---|
author | Bellido, Diego Abellán, Pablo Ruiz Palomar, José Manuel Álvarez Sintes, Rogelio Nubiolae, Andreu Bellido, Virginia Romero, Gracia |
author_facet | Bellido, Diego Abellán, Pablo Ruiz Palomar, José Manuel Álvarez Sintes, Rogelio Nubiolae, Andreu Bellido, Virginia Romero, Gracia |
author_sort | Bellido, Diego |
collection | PubMed |
description | BACKGROUND: Basal insulin reduces fasting blood glucose levels, but postprandial blood glucose levels may remain higher. Traditional strategies with rapid insulin intensification can cause hypoglycemic episodes and weight gain. Glucagon-like peptide-1 receptor agonists, such as the short-acting lixisenatide, are able to control postprandial excursions, without weight gain, and with a low risk of hypoglycemic events. OBJECTIVE: Due to the limited data on the combination of lixisenatide with basal insulin (with or without oral antidiabetes drugs) in clinical practice, this study evaluated changes in parameters associated with glycemic control and anthropometric data after 24 weeks of this therapy intensification. METHODS: This was a multicenter, retrospective observational study of 129 patients with type 2 diabetes that was uncontrolled by basal insulin. Their treatment was intensified by the addition of lixisenatide at least 24 weeks before being included in the study. Data were retrospectively collected to determine changes in glycated hemoglobin (HbA1c) levels, blood glucose levels, weight, and body mass index. Adverse reactions and hypoglycemic events were also recorded. RESULTS: After 24 weeks of therapy intensification with lixisenatide, a significant reduction in HbA1c levels was observed (–1.1%; P < 0.001). An HbA1c <7% was achieved in 30.2% of patients, and 17.1% reached an HbA1c <6.5%. There was a reduction in fasting blood glucose (31.8 [60.3] mg/dL; P < 0.001) and postprandial blood glucose (55.0 [49] mg/dL; P < 0.001) levels, as well as body weight (4.0 [5.4] kg; P < 0.001) and body mass index (1.5 [1.9]; P < 0.001). The most commonly observed adverse reactions were nausea (n = 9), in line with previous studies. Hypoglycemia events were rare; only reported in 2 patients. CONCLUSIONS: Intensification strategy based on lixisenatide added to basal insulin (with or without oral antidiabetes drugs) can be an effective treatment option in patients with uncontrolled type 2 diabetes. In this small, selected population, glycemic control was significantly improved in terms of HbA1, fasting blood glucose levels, and postprandial glucose levels, with a reduction of body weight and low risk of hypoglycemic events. (Curr Ther Res Clin Exp. 2018; 79:XXX–XXX) |
format | Online Article Text |
id | pubmed-6218842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62188422018-11-19 Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study Bellido, Diego Abellán, Pablo Ruiz Palomar, José Manuel Álvarez Sintes, Rogelio Nubiolae, Andreu Bellido, Virginia Romero, Gracia Curr Ther Res Clin Exp Original Research BACKGROUND: Basal insulin reduces fasting blood glucose levels, but postprandial blood glucose levels may remain higher. Traditional strategies with rapid insulin intensification can cause hypoglycemic episodes and weight gain. Glucagon-like peptide-1 receptor agonists, such as the short-acting lixisenatide, are able to control postprandial excursions, without weight gain, and with a low risk of hypoglycemic events. OBJECTIVE: Due to the limited data on the combination of lixisenatide with basal insulin (with or without oral antidiabetes drugs) in clinical practice, this study evaluated changes in parameters associated with glycemic control and anthropometric data after 24 weeks of this therapy intensification. METHODS: This was a multicenter, retrospective observational study of 129 patients with type 2 diabetes that was uncontrolled by basal insulin. Their treatment was intensified by the addition of lixisenatide at least 24 weeks before being included in the study. Data were retrospectively collected to determine changes in glycated hemoglobin (HbA1c) levels, blood glucose levels, weight, and body mass index. Adverse reactions and hypoglycemic events were also recorded. RESULTS: After 24 weeks of therapy intensification with lixisenatide, a significant reduction in HbA1c levels was observed (–1.1%; P < 0.001). An HbA1c <7% was achieved in 30.2% of patients, and 17.1% reached an HbA1c <6.5%. There was a reduction in fasting blood glucose (31.8 [60.3] mg/dL; P < 0.001) and postprandial blood glucose (55.0 [49] mg/dL; P < 0.001) levels, as well as body weight (4.0 [5.4] kg; P < 0.001) and body mass index (1.5 [1.9]; P < 0.001). The most commonly observed adverse reactions were nausea (n = 9), in line with previous studies. Hypoglycemia events were rare; only reported in 2 patients. CONCLUSIONS: Intensification strategy based on lixisenatide added to basal insulin (with or without oral antidiabetes drugs) can be an effective treatment option in patients with uncontrolled type 2 diabetes. In this small, selected population, glycemic control was significantly improved in terms of HbA1, fasting blood glucose levels, and postprandial glucose levels, with a reduction of body weight and low risk of hypoglycemic events. (Curr Ther Res Clin Exp. 2018; 79:XXX–XXX) Elsevier 2018-10-09 /pmc/articles/PMC6218842/ /pubmed/30455779 http://dx.doi.org/10.1016/j.curtheres.2018.09.001 Text en © 2018 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Bellido, Diego Abellán, Pablo Ruiz Palomar, José Manuel Álvarez Sintes, Rogelio Nubiolae, Andreu Bellido, Virginia Romero, Gracia Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study |
title | Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study |
title_full | Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study |
title_fullStr | Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study |
title_full_unstemmed | Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study |
title_short | Intensification of Basal Insulin Therapy with Lixisenatide in Patients with Type 2 Diabetes in a Real-World Setting: The BASAL-LIXI Study |
title_sort | intensification of basal insulin therapy with lixisenatide in patients with type 2 diabetes in a real-world setting: the basal-lixi study |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6218842/ https://www.ncbi.nlm.nih.gov/pubmed/30455779 http://dx.doi.org/10.1016/j.curtheres.2018.09.001 |
work_keys_str_mv | AT bellidodiego intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy AT abellanpablo intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy AT ruizpalomarjosemanuel intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy AT alvarezsintesrogelio intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy AT nubiolaeandreu intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy AT bellidovirginia intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy AT romerogracia intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy AT intensificationofbasalinsulintherapywithlixisenatideinpatientswithtype2diabetesinarealworldsettingthebasallixistudy |