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Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients

AIMS: A close association has been demonstrated between increased cardiovascular risk and high asymmetric dimethylarginine (ADMA) levels in type 2 diabetes mellitus (DM) patients. We planned to measure serum ADMA levels in type 2 DM patients using vildagliptin, a dipeptidyl peptidase-4 (DPP-4) inhib...

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Autores principales: Cakirca, Mustafa, Karatoprak, Cumali, Zorlu, Mehmet, Kiskac, Muharrem, Kanat, Mustafa, Cikrikcioglu, Mehmet Ali, Soysal, Pinar, Hursitoglu, Mehmet, Camli, Ahmet Adil, Erkoc, Reha, Abdul-Ghani, Muhammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931658/
https://www.ncbi.nlm.nih.gov/pubmed/24627624
http://dx.doi.org/10.2147/DDDT.S52545
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author Cakirca, Mustafa
Karatoprak, Cumali
Zorlu, Mehmet
Kiskac, Muharrem
Kanat, Mustafa
Cikrikcioglu, Mehmet Ali
Soysal, Pinar
Hursitoglu, Mehmet
Camli, Ahmet Adil
Erkoc, Reha
Abdul-Ghani, Muhammad
author_facet Cakirca, Mustafa
Karatoprak, Cumali
Zorlu, Mehmet
Kiskac, Muharrem
Kanat, Mustafa
Cikrikcioglu, Mehmet Ali
Soysal, Pinar
Hursitoglu, Mehmet
Camli, Ahmet Adil
Erkoc, Reha
Abdul-Ghani, Muhammad
author_sort Cakirca, Mustafa
collection PubMed
description AIMS: A close association has been demonstrated between increased cardiovascular risk and high asymmetric dimethylarginine (ADMA) levels in type 2 diabetes mellitus (DM) patients. We planned to measure serum ADMA levels in type 2 DM patients using vildagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor. MATERIALS AND METHODS: A total of 68 type 2 DM patients who were on metformin were enrolled in the study. Based on the glycemic levels of patients, vildagliptin was added on to treatment in 33 patients. Patients were followed for 6 months. Serum ADMA, C-reactive protein, and fibrinogen levels were compared in groups of patients using metformin or metformin + vildagliptin, after 6 months. RESULTS: Serum ADMA levels were found to be significantly lower in the group using vildagliptin compared to the group using metformin + vildagliptin (P<0.001). However, serum C-reactive protein and fibrinogen levels were statistically similar in the two study groups (P=0.34 and P=0.23, respectively). CONCLUSION: Metformin + vildagliptin treatment was observed to lower serum ADMA levels in type 2 DM patients. Our findings notwithstanding, large-scale prospective randomized controlled studies are warranted to conclude that vildagliptin provides cardiovascular protection along with diabetes regulation.
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spelling pubmed-39316582014-03-13 Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients Cakirca, Mustafa Karatoprak, Cumali Zorlu, Mehmet Kiskac, Muharrem Kanat, Mustafa Cikrikcioglu, Mehmet Ali Soysal, Pinar Hursitoglu, Mehmet Camli, Ahmet Adil Erkoc, Reha Abdul-Ghani, Muhammad Drug Des Devel Ther Original Research AIMS: A close association has been demonstrated between increased cardiovascular risk and high asymmetric dimethylarginine (ADMA) levels in type 2 diabetes mellitus (DM) patients. We planned to measure serum ADMA levels in type 2 DM patients using vildagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor. MATERIALS AND METHODS: A total of 68 type 2 DM patients who were on metformin were enrolled in the study. Based on the glycemic levels of patients, vildagliptin was added on to treatment in 33 patients. Patients were followed for 6 months. Serum ADMA, C-reactive protein, and fibrinogen levels were compared in groups of patients using metformin or metformin + vildagliptin, after 6 months. RESULTS: Serum ADMA levels were found to be significantly lower in the group using vildagliptin compared to the group using metformin + vildagliptin (P<0.001). However, serum C-reactive protein and fibrinogen levels were statistically similar in the two study groups (P=0.34 and P=0.23, respectively). CONCLUSION: Metformin + vildagliptin treatment was observed to lower serum ADMA levels in type 2 DM patients. Our findings notwithstanding, large-scale prospective randomized controlled studies are warranted to conclude that vildagliptin provides cardiovascular protection along with diabetes regulation. Dove Medical Press 2014-02-14 /pmc/articles/PMC3931658/ /pubmed/24627624 http://dx.doi.org/10.2147/DDDT.S52545 Text en © 2014 Cakirca et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Cakirca, Mustafa
Karatoprak, Cumali
Zorlu, Mehmet
Kiskac, Muharrem
Kanat, Mustafa
Cikrikcioglu, Mehmet Ali
Soysal, Pinar
Hursitoglu, Mehmet
Camli, Ahmet Adil
Erkoc, Reha
Abdul-Ghani, Muhammad
Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients
title Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients
title_full Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients
title_fullStr Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients
title_full_unstemmed Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients
title_short Effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients
title_sort effect of vildagliptin add-on treatment to metformin on plasma asymmetric dimethylarginine in type 2 diabetes mellitus patients
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3931658/
https://www.ncbi.nlm.nih.gov/pubmed/24627624
http://dx.doi.org/10.2147/DDDT.S52545
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