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Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting
BACKGROUND: Inhibitors of dipeptidyl-peptidase IV are recommended as second-line therapy in type 2 diabetes (DT2), but data, as a first-line treatment in everyday clinical practice are scarce. To address this issue we conducted a 12-month, clinical study in an outpatient setting, using vildagliptin...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563902/ https://www.ncbi.nlm.nih.gov/pubmed/26355765 http://dx.doi.org/10.1186/s40200-015-0194-6 |
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author | Yavropoulou, M. P. Pikilidou, M. Kotsa, K. Michopoulos, A. Papakonstantinou, E. Yovos, J. G. |
author_facet | Yavropoulou, M. P. Pikilidou, M. Kotsa, K. Michopoulos, A. Papakonstantinou, E. Yovos, J. G. |
author_sort | Yavropoulou, M. P. |
collection | PubMed |
description | BACKGROUND: Inhibitors of dipeptidyl-peptidase IV are recommended as second-line therapy in type 2 diabetes (DT2), but data, as a first-line treatment in everyday clinical practice are scarce. To address this issue we conducted a 12-month, clinical study in an outpatient setting, using vildagliptin as the first-line treatment. METHODS: Ninety-one drug naïve patients with DT2 started with vildagliptin monotherapy (100 mg daily) for 4 months and were scheduled to regular 4-monthly visits for 1 year. Patients received add-on treatment with metformin or metformin and glimepiride according to their glycosylated hemoglobin (HbA1c) at each study-visit. RESULTS: HbA1c was significantly decreased with vildagliptin monotherapy from 8.16 % ± 1.60 to 7.52 % ± 1.60, p < 0.001. Only 39 % of the patients achieved the target of HbA1c ≤ 7.0 % at the end of the 4th month. Mean change in HbA1c was significantly correlated with baseline HbA1c values (r = −0.51, p < 0.001). At the end of the study only 35 % of the patients remained on vildagliptin monotherapy while the rest required add-on treatment with metformin or metformin and sulfonylurea. CONCLUSIONS: Vildagliptin is well tolerated either as monotherapy or in combination but the majority of patients require add-on therapy shortly after the beginning of treatment. |
format | Online Article Text |
id | pubmed-4563902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-45639022015-09-10 Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting Yavropoulou, M. P. Pikilidou, M. Kotsa, K. Michopoulos, A. Papakonstantinou, E. Yovos, J. G. J Diabetes Metab Disord Research Article BACKGROUND: Inhibitors of dipeptidyl-peptidase IV are recommended as second-line therapy in type 2 diabetes (DT2), but data, as a first-line treatment in everyday clinical practice are scarce. To address this issue we conducted a 12-month, clinical study in an outpatient setting, using vildagliptin as the first-line treatment. METHODS: Ninety-one drug naïve patients with DT2 started with vildagliptin monotherapy (100 mg daily) for 4 months and were scheduled to regular 4-monthly visits for 1 year. Patients received add-on treatment with metformin or metformin and glimepiride according to their glycosylated hemoglobin (HbA1c) at each study-visit. RESULTS: HbA1c was significantly decreased with vildagliptin monotherapy from 8.16 % ± 1.60 to 7.52 % ± 1.60, p < 0.001. Only 39 % of the patients achieved the target of HbA1c ≤ 7.0 % at the end of the 4th month. Mean change in HbA1c was significantly correlated with baseline HbA1c values (r = −0.51, p < 0.001). At the end of the study only 35 % of the patients remained on vildagliptin monotherapy while the rest required add-on treatment with metformin or metformin and sulfonylurea. CONCLUSIONS: Vildagliptin is well tolerated either as monotherapy or in combination but the majority of patients require add-on therapy shortly after the beginning of treatment. BioMed Central 2015-08-22 /pmc/articles/PMC4563902/ /pubmed/26355765 http://dx.doi.org/10.1186/s40200-015-0194-6 Text en © Yavropoulou et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Yavropoulou, M. P. Pikilidou, M. Kotsa, K. Michopoulos, A. Papakonstantinou, E. Yovos, J. G. Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting |
title | Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting |
title_full | Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting |
title_fullStr | Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting |
title_full_unstemmed | Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting |
title_short | Efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting |
title_sort | efficacy and tolerability of vildagliptin as first line treatment in patients with diabetes type 2 in an outpatient setting |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4563902/ https://www.ncbi.nlm.nih.gov/pubmed/26355765 http://dx.doi.org/10.1186/s40200-015-0194-6 |
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