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Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus
We performed a network meta-analysis to compare the efficacy of 12 single-drug regimens (Glibenclamide, Glimepiride, Pioglitazone, Rosiglitazone, Repaglinide, Metformin, Sitaglitin, Exenatide, Liraglutide, Acarbose, Benfluorex, and Glipizide) in the treatment of type 2 diabetes mellitus (T2DM). Fift...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641162/ https://www.ncbi.nlm.nih.gov/pubmed/29069819 http://dx.doi.org/10.18632/oncotarget.20282 |
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author | Wang, Shao-Lian Dong, Wen-Bin Dong, Xiao-Lin Zhu, Wen-Min Wang, Fang-Fang Han, Fang Yan, Xin |
author_facet | Wang, Shao-Lian Dong, Wen-Bin Dong, Xiao-Lin Zhu, Wen-Min Wang, Fang-Fang Han, Fang Yan, Xin |
author_sort | Wang, Shao-Lian |
collection | PubMed |
description | We performed a network meta-analysis to compare the efficacy of 12 single-drug regimens (Glibenclamide, Glimepiride, Pioglitazone, Rosiglitazone, Repaglinide, Metformin, Sitaglitin, Exenatide, Liraglutide, Acarbose, Benfluorex, and Glipizide) in the treatment of type 2 diabetes mellitus (T2DM). Fifteen relevant randomized controlled trials (RCTs) were included; direct and indirect evidence from these studies was combined, and weighted mean difference (WMD) and surface under the cumulative ranking curves (SUCRAs) were examined to evaluate the monotherapies. Liraglutide was more effective than Glimepiride, Pioglitazone, Sitaglitin, Exenatide, and Glipizide at reducing glycated hemoglobin (HbA1c) levels. In contrast, Acarbose was less effective than Glibenclamide, Glimepiride, Pioglitazone, Rosiglitazone, Repaglinide, Metformin, and Liraglutide at decreasing HbA1c levels. Reductions in fasting plasma glucose (FPG) levels were similar after all treatments. Rosiglitazone was less effective than Glibenclamide and Repaglinide at reducing total cholesterol (TC) levels. High density lipoprotein (HDL), low density lipoprotein (LDL), and triglyceride levels did not differ after treatment with any of the monotherapies. HbA1c and FPG SUCRA values were highest for Liraglutide, while HbA1c and FPG values were lowest for Acarbose, and TC and LDL values were lowest for Rosiglitazone. These results suggest that Liraglutide may be most effective, and Acarbose least effective, at reducing blood glucose levels, while Glibenclamide, Repaglinide, and Metformin may be most effective, and Rosiglitazone least effective, at reducing lipoidemia, in T2DM patients. |
format | Online Article Text |
id | pubmed-5641162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56411622017-10-24 Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus Wang, Shao-Lian Dong, Wen-Bin Dong, Xiao-Lin Zhu, Wen-Min Wang, Fang-Fang Han, Fang Yan, Xin Oncotarget Research Paper We performed a network meta-analysis to compare the efficacy of 12 single-drug regimens (Glibenclamide, Glimepiride, Pioglitazone, Rosiglitazone, Repaglinide, Metformin, Sitaglitin, Exenatide, Liraglutide, Acarbose, Benfluorex, and Glipizide) in the treatment of type 2 diabetes mellitus (T2DM). Fifteen relevant randomized controlled trials (RCTs) were included; direct and indirect evidence from these studies was combined, and weighted mean difference (WMD) and surface under the cumulative ranking curves (SUCRAs) were examined to evaluate the monotherapies. Liraglutide was more effective than Glimepiride, Pioglitazone, Sitaglitin, Exenatide, and Glipizide at reducing glycated hemoglobin (HbA1c) levels. In contrast, Acarbose was less effective than Glibenclamide, Glimepiride, Pioglitazone, Rosiglitazone, Repaglinide, Metformin, and Liraglutide at decreasing HbA1c levels. Reductions in fasting plasma glucose (FPG) levels were similar after all treatments. Rosiglitazone was less effective than Glibenclamide and Repaglinide at reducing total cholesterol (TC) levels. High density lipoprotein (HDL), low density lipoprotein (LDL), and triglyceride levels did not differ after treatment with any of the monotherapies. HbA1c and FPG SUCRA values were highest for Liraglutide, while HbA1c and FPG values were lowest for Acarbose, and TC and LDL values were lowest for Rosiglitazone. These results suggest that Liraglutide may be most effective, and Acarbose least effective, at reducing blood glucose levels, while Glibenclamide, Repaglinide, and Metformin may be most effective, and Rosiglitazone least effective, at reducing lipoidemia, in T2DM patients. Impact Journals LLC 2017-08-16 /pmc/articles/PMC5641162/ /pubmed/29069819 http://dx.doi.org/10.18632/oncotarget.20282 Text en Copyright: © 2017 Wang et al. http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Research Paper Wang, Shao-Lian Dong, Wen-Bin Dong, Xiao-Lin Zhu, Wen-Min Wang, Fang-Fang Han, Fang Yan, Xin Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus |
title | Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus |
title_full | Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus |
title_fullStr | Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus |
title_full_unstemmed | Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus |
title_short | Comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus |
title_sort | comparison of twelve single-drug regimens for the treatment of type 2 diabetes mellitus |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5641162/ https://www.ncbi.nlm.nih.gov/pubmed/29069819 http://dx.doi.org/10.18632/oncotarget.20282 |
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