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Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin?
INTRODUCTION: Diagnosis and initial management of diabetes mellitus (DM) in the young are clinical dilemma. Gliptins may be a safer and more effective option than sulfonylureas. Few Indian studies have addressed this issue of clinical relevance. AIM: To compare the use of sitagliptin and glimepiride...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3603119/ https://www.ncbi.nlm.nih.gov/pubmed/23565471 http://dx.doi.org/10.4103/2230-8210.104136 |
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author | Muthukrishnan, J. Dawra, S. Marwaha, V. Bishnoi, J. S. Narayanan, C. S. |
author_facet | Muthukrishnan, J. Dawra, S. Marwaha, V. Bishnoi, J. S. Narayanan, C. S. |
author_sort | Muthukrishnan, J. |
collection | PubMed |
description | INTRODUCTION: Diagnosis and initial management of diabetes mellitus (DM) in the young are clinical dilemma. Gliptins may be a safer and more effective option than sulfonylureas. Few Indian studies have addressed this issue of clinical relevance. AIM: To compare the use of sitagliptin and glimepiride as early add-on drugs along with metformin in young patients with DM to achieve optimum glycemic targets. METHODS: This was a prospective, open-label, cohort study set in a tertiary care hospital in North India. Newly diagnosed patients of DM ≤35 year of age were initially treated to pre-defined glycemic goals (Fasting plasma glucose (FPG) 70-130, post prandial glucose (PPG) < 180 mg/dl) with insulin and metformin 1 g for 8 weeks. Insulin was discontinued and metformin increased to 2 g daily for next 4 weeks. Thereafter, glimepiride 1 mg or sitagliptin 100 mg was randomly added to those who were not maintaining the set glucose targets. Dose of glimepiride was uptitrated every 4 weeks upto a maximum of 4 mg. Three groups (Gp A: Metfromin 2 g/d, Gp B: Metformin 2 g + Glimepiride 1-4 mg/d, and Gp C: Metformin 2 g + sitagliptin 100 mg/d) were followed up over next 24 weeks. They were compared for glycemic control and weight change. Those failing therapy on these drugs (FPG > 180, PPG > 250 mg/dl with/without catabolic symptoms/ketosis) were withdrawn. RESULTS: Sitagliptin with metfromin and metfromin alone group fared better than the glimepiride group for glycemic control, lesser treatment failures, and less weight gain. CONCLUSION: In this limited study, we found that sitagliptin is a safer and more effective option in young, newly diagnosed patients with DM. Findings of this study are relevant for clinical practice in Indian setting. |
format | Online Article Text |
id | pubmed-3603119 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-36031192013-04-05 Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin? Muthukrishnan, J. Dawra, S. Marwaha, V. Bishnoi, J. S. Narayanan, C. S. Indian J Endocrinol Metab Brief Communication INTRODUCTION: Diagnosis and initial management of diabetes mellitus (DM) in the young are clinical dilemma. Gliptins may be a safer and more effective option than sulfonylureas. Few Indian studies have addressed this issue of clinical relevance. AIM: To compare the use of sitagliptin and glimepiride as early add-on drugs along with metformin in young patients with DM to achieve optimum glycemic targets. METHODS: This was a prospective, open-label, cohort study set in a tertiary care hospital in North India. Newly diagnosed patients of DM ≤35 year of age were initially treated to pre-defined glycemic goals (Fasting plasma glucose (FPG) 70-130, post prandial glucose (PPG) < 180 mg/dl) with insulin and metformin 1 g for 8 weeks. Insulin was discontinued and metformin increased to 2 g daily for next 4 weeks. Thereafter, glimepiride 1 mg or sitagliptin 100 mg was randomly added to those who were not maintaining the set glucose targets. Dose of glimepiride was uptitrated every 4 weeks upto a maximum of 4 mg. Three groups (Gp A: Metfromin 2 g/d, Gp B: Metformin 2 g + Glimepiride 1-4 mg/d, and Gp C: Metformin 2 g + sitagliptin 100 mg/d) were followed up over next 24 weeks. They were compared for glycemic control and weight change. Those failing therapy on these drugs (FPG > 180, PPG > 250 mg/dl with/without catabolic symptoms/ketosis) were withdrawn. RESULTS: Sitagliptin with metfromin and metfromin alone group fared better than the glimepiride group for glycemic control, lesser treatment failures, and less weight gain. CONCLUSION: In this limited study, we found that sitagliptin is a safer and more effective option in young, newly diagnosed patients with DM. Findings of this study are relevant for clinical practice in Indian setting. Medknow Publications & Media Pvt Ltd 2012-12 /pmc/articles/PMC3603119/ /pubmed/23565471 http://dx.doi.org/10.4103/2230-8210.104136 Text en Copyright: © Indian Journal of Endocrinology and Metabolism http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Brief Communication Muthukrishnan, J. Dawra, S. Marwaha, V. Bishnoi, J. S. Narayanan, C. S. Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin? |
title | Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin? |
title_full | Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin? |
title_fullStr | Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin? |
title_full_unstemmed | Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin? |
title_short | Diabetes mellitus in the young: Gliptins or sulfonylurea after metformin? |
title_sort | diabetes mellitus in the young: gliptins or sulfonylurea after metformin? |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3603119/ https://www.ncbi.nlm.nih.gov/pubmed/23565471 http://dx.doi.org/10.4103/2230-8210.104136 |
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