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Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus

OBJECTIVE: To share our clinical experience with exenatide in obese North Indian subjects with type 2 diabetes. MATERIALS AND METHODS: We share our experience with use of exenatide in 74 patients treated at Indraprastha Apollo Hospital, a tertiary care centre in New Delhi, India Subjects included ob...

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Autores principales: Bawa, Tarunika, Dhingra, Vibha, Malhotra, Nidhi, Wasir, Jasjeet S., Mithal, Ambrish
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659913/
https://www.ncbi.nlm.nih.gov/pubmed/23776858
http://dx.doi.org/10.4103/2230-8210.107804
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author Bawa, Tarunika
Dhingra, Vibha
Malhotra, Nidhi
Wasir, Jasjeet S.
Mithal, Ambrish
author_facet Bawa, Tarunika
Dhingra, Vibha
Malhotra, Nidhi
Wasir, Jasjeet S.
Mithal, Ambrish
author_sort Bawa, Tarunika
collection PubMed
description OBJECTIVE: To share our clinical experience with exenatide in obese North Indian subjects with type 2 diabetes. MATERIALS AND METHODS: We share our experience with use of exenatide in 74 patients treated at Indraprastha Apollo Hospital, a tertiary care centre in New Delhi, India Subjects included obese / overweight subjects (mean weight and BMI; 97.67 ± 5.6 kg and 34.56 kg/m(2)) with known history of type 2 DM (Mean: 9 ± 5.6 years) and maintaining suboptimal glycemic control (HbA1c >7%) on oral antidiabetic agents, with or without basal insulin. Metformin and sulphonylureas were continued (with dose adjustment if indicated), as was basal insulin (glargine / detemir). TZDs and DPP4 inhibitors were discontinued. The dose of exenatide was increased to 10 mcg twice a day after 4-12 weeks. 56 patients completed minimum 3 month therapy. 42 patients completed 6 months, 32, 9 months and 25 completed 12 months. Data of patients who had completed at-least 3 months of therapy was included for analysis. RESULTS AND DISCUSSION: 69.77, 67.44, and 13.95% of the patients were receiving metformin, secretagogues or thiazolidinediones alone or in combination; 17.76% of the patients were on basal insulin. The change in fasting and post-prandial blood glucose levels were significant at 3, 6, 9 and 12 months with p-value <0.05. The mean weight loss at one, three, and six months and one year was 1.7 ± 1.3, 3.8 ± 2.5, 6.3 ± 3.4, and 8.3 ± 4.3 kg, respectively (P <0.05). The mean HbA1c (baseline: 8.8 ± 1.3%) at 3, 6 months and at one year was 7.8 ± 0.9, 7.7 ± 0.8 and 7.2 ± 0.8 (P <0.05). Thirty-five percent of the patients had a ‘good’ A1c value (< 7%) at the end of 12 months. 13 patients discontinued exenatide (three due to lack of response, six due to cost of therapy and four due to severe nausea). Nausea was the most common side effect, occurring in 95% patients within 1 month, although the incidence declined with passage of time. CONCLUSIONS: Clinical use of Exenatide is associated with significant improvement in glycemic control and major weight loss (8.3±4.3 kg at 1 year) in obese subjects with type 2 diabetes. Nausea is the most common side effect. In conclusion, exenatide is a effective and useful option for treatment of type 2 diabetes in obese Indian subjects.
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spelling pubmed-36599132013-06-17 Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus Bawa, Tarunika Dhingra, Vibha Malhotra, Nidhi Wasir, Jasjeet S. Mithal, Ambrish Indian J Endocrinol Metab Original Article OBJECTIVE: To share our clinical experience with exenatide in obese North Indian subjects with type 2 diabetes. MATERIALS AND METHODS: We share our experience with use of exenatide in 74 patients treated at Indraprastha Apollo Hospital, a tertiary care centre in New Delhi, India Subjects included obese / overweight subjects (mean weight and BMI; 97.67 ± 5.6 kg and 34.56 kg/m(2)) with known history of type 2 DM (Mean: 9 ± 5.6 years) and maintaining suboptimal glycemic control (HbA1c >7%) on oral antidiabetic agents, with or without basal insulin. Metformin and sulphonylureas were continued (with dose adjustment if indicated), as was basal insulin (glargine / detemir). TZDs and DPP4 inhibitors were discontinued. The dose of exenatide was increased to 10 mcg twice a day after 4-12 weeks. 56 patients completed minimum 3 month therapy. 42 patients completed 6 months, 32, 9 months and 25 completed 12 months. Data of patients who had completed at-least 3 months of therapy was included for analysis. RESULTS AND DISCUSSION: 69.77, 67.44, and 13.95% of the patients were receiving metformin, secretagogues or thiazolidinediones alone or in combination; 17.76% of the patients were on basal insulin. The change in fasting and post-prandial blood glucose levels were significant at 3, 6, 9 and 12 months with p-value <0.05. The mean weight loss at one, three, and six months and one year was 1.7 ± 1.3, 3.8 ± 2.5, 6.3 ± 3.4, and 8.3 ± 4.3 kg, respectively (P <0.05). The mean HbA1c (baseline: 8.8 ± 1.3%) at 3, 6 months and at one year was 7.8 ± 0.9, 7.7 ± 0.8 and 7.2 ± 0.8 (P <0.05). Thirty-five percent of the patients had a ‘good’ A1c value (< 7%) at the end of 12 months. 13 patients discontinued exenatide (three due to lack of response, six due to cost of therapy and four due to severe nausea). Nausea was the most common side effect, occurring in 95% patients within 1 month, although the incidence declined with passage of time. CONCLUSIONS: Clinical use of Exenatide is associated with significant improvement in glycemic control and major weight loss (8.3±4.3 kg at 1 year) in obese subjects with type 2 diabetes. Nausea is the most common side effect. In conclusion, exenatide is a effective and useful option for treatment of type 2 diabetes in obese Indian subjects. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3659913/ /pubmed/23776858 http://dx.doi.org/10.4103/2230-8210.107804 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 Original Article
Bawa, Tarunika
Dhingra, Vibha
Malhotra, Nidhi
Wasir, Jasjeet S.
Mithal, Ambrish
Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus
title Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus
title_full Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus
title_fullStr Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus
title_full_unstemmed Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus
title_short Clinical experience with exenatide in obese North Indian patients with type 2 diabetes mellitus
title_sort clinical experience with exenatide in obese north indian patients with type 2 diabetes mellitus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3659913/
https://www.ncbi.nlm.nih.gov/pubmed/23776858
http://dx.doi.org/10.4103/2230-8210.107804
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