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Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index
This study investigated the effects of switching from combination therapy with either alogliptin (Alo) or pioglitazone (Pio) to fixed-dose combination therapy (FDCT) with alogliptin and pioglitazone (Alo-Pio FDCT). The usefulness and efficacy of Alo-Pio FDCT were investigated. A total of 50 outpatie...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nagoya University
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346615/ https://www.ncbi.nlm.nih.gov/pubmed/28303056 http://dx.doi.org/10.18999/nagjms.79.1.9 |
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author | Aoki, Chie Suzuki, Kunihiro Kuroda, Hisamoto Sagara, Masaaki Shimizu, Masanori Kasai, Kikuo Aso, Yoshimasa |
author_facet | Aoki, Chie Suzuki, Kunihiro Kuroda, Hisamoto Sagara, Masaaki Shimizu, Masanori Kasai, Kikuo Aso, Yoshimasa |
author_sort | Aoki, Chie |
collection | PubMed |
description | This study investigated the effects of switching from combination therapy with either alogliptin (Alo) or pioglitazone (Pio) to fixed-dose combination therapy (FDCT) with alogliptin and pioglitazone (Alo-Pio FDCT). The usefulness and efficacy of Alo-Pio FDCT were investigated. A total of 50 outpatients with type 2 diabetes mellitus (T2DM) treated with Alo and 47 outpatients with T2DM treated with Pio were switched to Alo-Pio FDCT, and its efficacy and usefulness were evaluated. Significant improvements were observed in hemoglobinA1c (HbA(1c)), alanine transaminase (ALT), and γ-glutamyl transpeptidase (GGT) levels after switching to Alo-Pio FDCT for 16 weeks in both groups. Only the group switching from Alo to Alo-Pio FDCT showed significant improvements in high-density lipoprotein cholesterol (HDL) levels and triglyceride levels. In a multivariate logistic regression model of the variation in the change of HbA(1c) at 16 weeks, ALT and GGT were independent predictors of the change of HbA(1c) at 16 weeks. In addition, the switch to Alo-Pio FDCT improved glycemic control to a certain degree regardless of BMI. Switching from either Alo or Pio to Alo-PIO FDCT may, unlike monotherapy with a DPP-4 inhibitor, be effective for patients with T2DM regardless of whether they are obese or lean. |
format | Online Article Text |
id | pubmed-5346615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nagoya University |
record_format | MEDLINE/PubMed |
spelling | pubmed-53466152017-03-16 Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index Aoki, Chie Suzuki, Kunihiro Kuroda, Hisamoto Sagara, Masaaki Shimizu, Masanori Kasai, Kikuo Aso, Yoshimasa Nagoya J Med Sci Original Paper This study investigated the effects of switching from combination therapy with either alogliptin (Alo) or pioglitazone (Pio) to fixed-dose combination therapy (FDCT) with alogliptin and pioglitazone (Alo-Pio FDCT). The usefulness and efficacy of Alo-Pio FDCT were investigated. A total of 50 outpatients with type 2 diabetes mellitus (T2DM) treated with Alo and 47 outpatients with T2DM treated with Pio were switched to Alo-Pio FDCT, and its efficacy and usefulness were evaluated. Significant improvements were observed in hemoglobinA1c (HbA(1c)), alanine transaminase (ALT), and γ-glutamyl transpeptidase (GGT) levels after switching to Alo-Pio FDCT for 16 weeks in both groups. Only the group switching from Alo to Alo-Pio FDCT showed significant improvements in high-density lipoprotein cholesterol (HDL) levels and triglyceride levels. In a multivariate logistic regression model of the variation in the change of HbA(1c) at 16 weeks, ALT and GGT were independent predictors of the change of HbA(1c) at 16 weeks. In addition, the switch to Alo-Pio FDCT improved glycemic control to a certain degree regardless of BMI. Switching from either Alo or Pio to Alo-PIO FDCT may, unlike monotherapy with a DPP-4 inhibitor, be effective for patients with T2DM regardless of whether they are obese or lean. Nagoya University 2017-02 /pmc/articles/PMC5346615/ /pubmed/28303056 http://dx.doi.org/10.18999/nagjms.79.1.9 Text en http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view the details of this license, please visit (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Paper Aoki, Chie Suzuki, Kunihiro Kuroda, Hisamoto Sagara, Masaaki Shimizu, Masanori Kasai, Kikuo Aso, Yoshimasa Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index |
title | Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index |
title_full | Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index |
title_fullStr | Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index |
title_full_unstemmed | Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index |
title_short | Fixed-dose combination of alogliptin/pioglitazone improves glycemic control in Japanese patients with type 2 diabetes mellitus independent of body mass index |
title_sort | fixed-dose combination of alogliptin/pioglitazone improves glycemic control in japanese patients with type 2 diabetes mellitus independent of body mass index |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346615/ https://www.ncbi.nlm.nih.gov/pubmed/28303056 http://dx.doi.org/10.18999/nagjms.79.1.9 |
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