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Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients
INTRODUCTION: Anagliptin (ANA) improves dyslipidemia in addition to blood glucose levels. However, there are no comparative studies on the effects of ANA and other dipeptidyl peptidase‐4 inhibitors on serum lipid profile. We compared the effects of ANA on serum lipid profile with those of alogliptin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835469/ https://www.ncbi.nlm.nih.gov/pubmed/28853228 http://dx.doi.org/10.1111/jdi.12739 |
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author | Kurozumi, Akira Okada, Yosuke Arao, Tadashi Kobayashi, Takuya Masuda, Daisaku Yamashita, Shizuya Tanaka, Yoshiya |
author_facet | Kurozumi, Akira Okada, Yosuke Arao, Tadashi Kobayashi, Takuya Masuda, Daisaku Yamashita, Shizuya Tanaka, Yoshiya |
author_sort | Kurozumi, Akira |
collection | PubMed |
description | INTRODUCTION: Anagliptin (ANA) improves dyslipidemia in addition to blood glucose levels. However, there are no comparative studies on the effects of ANA and other dipeptidyl peptidase‐4 inhibitors on serum lipid profile. We compared the effects of ANA on serum lipid profile with those of alogliptin (ALO) in type 2 diabetes mellitus outpatients. MATERIALS AND METHODS: The study participants were 87 type 2 diabetes mellitus patients who had been treated with dipeptidyl peptidase‐4 inhibitors for ≥8 weeks and had a low‐density lipoprotein cholesterol (LDL‐C) level of ≥120 mg/dL. Participants were switched to either 200 mg/day ANA or 25 mg/day ALO for 24 weeks. RESULTS: There was no significant difference in percentage change in LDL‐C level at 24 weeks between the ANA and ALO groups. Treatment with ANA for 12 weeks significantly decreased LDL‐C levels, one of the secondary end‐points. Treatment with ANA for 24 weeks significantly improved apolipoprotein B‐100 levels, and the percentage change in LDL‐C levels at 24 weeks correlated significantly with the percentage change in apolipoprotein B‐100 levels in the ANA group. CONCLUSIONS: The LDL‐C‐lowering effects of ANA and ALO at 24 weeks were almost similar in patients with type 2 diabetes mellitus. However, the results showed a tendency for a decrease in LDL‐C level at 24 weeks in the ANA group, and that such improvement was mediated, at least in part, through the suppression of apolipoprotein B‐100 synthesis. |
format | Online Article Text |
id | pubmed-5835469 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58354692018-03-07 Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients Kurozumi, Akira Okada, Yosuke Arao, Tadashi Kobayashi, Takuya Masuda, Daisaku Yamashita, Shizuya Tanaka, Yoshiya J Diabetes Investig Articles INTRODUCTION: Anagliptin (ANA) improves dyslipidemia in addition to blood glucose levels. However, there are no comparative studies on the effects of ANA and other dipeptidyl peptidase‐4 inhibitors on serum lipid profile. We compared the effects of ANA on serum lipid profile with those of alogliptin (ALO) in type 2 diabetes mellitus outpatients. MATERIALS AND METHODS: The study participants were 87 type 2 diabetes mellitus patients who had been treated with dipeptidyl peptidase‐4 inhibitors for ≥8 weeks and had a low‐density lipoprotein cholesterol (LDL‐C) level of ≥120 mg/dL. Participants were switched to either 200 mg/day ANA or 25 mg/day ALO for 24 weeks. RESULTS: There was no significant difference in percentage change in LDL‐C level at 24 weeks between the ANA and ALO groups. Treatment with ANA for 12 weeks significantly decreased LDL‐C levels, one of the secondary end‐points. Treatment with ANA for 24 weeks significantly improved apolipoprotein B‐100 levels, and the percentage change in LDL‐C levels at 24 weeks correlated significantly with the percentage change in apolipoprotein B‐100 levels in the ANA group. CONCLUSIONS: The LDL‐C‐lowering effects of ANA and ALO at 24 weeks were almost similar in patients with type 2 diabetes mellitus. However, the results showed a tendency for a decrease in LDL‐C level at 24 weeks in the ANA group, and that such improvement was mediated, at least in part, through the suppression of apolipoprotein B‐100 synthesis. John Wiley and Sons Inc. 2017-10-03 2018-03 /pmc/articles/PMC5835469/ /pubmed/28853228 http://dx.doi.org/10.1111/jdi.12739 Text en © 2017 The Authors. Journal of Diabetes Investigation published by Asian Association for the Study of Diabetes (AASD) and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Articles Kurozumi, Akira Okada, Yosuke Arao, Tadashi Kobayashi, Takuya Masuda, Daisaku Yamashita, Shizuya Tanaka, Yoshiya Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients |
title | Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients |
title_full | Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients |
title_fullStr | Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients |
title_full_unstemmed | Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients |
title_short | Comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients |
title_sort | comparison of effects of anagliptin and alogliptin on serum lipid profile in type 2 diabetes mellitus patients |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835469/ https://www.ncbi.nlm.nih.gov/pubmed/28853228 http://dx.doi.org/10.1111/jdi.12739 |
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