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Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus

AIM: In the present study, we investigated the long-term effects of exenatide treatment on serum fasting ghrelin levels in patients with type 2 diabetes mellitus. METHODS: Type 2 diabetic patients, who were using metformin with and without the other antihyperglycemic drugs on a stable dose for at le...

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Autores principales: Guclu, Metin, Kiyici, Sinem, Gul, Zulfiye, Cavun, Sinan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776666/
https://www.ncbi.nlm.nih.gov/pubmed/29217653
http://dx.doi.org/10.1530/EC-17-0242
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author Guclu, Metin
Kiyici, Sinem
Gul, Zulfiye
Cavun, Sinan
author_facet Guclu, Metin
Kiyici, Sinem
Gul, Zulfiye
Cavun, Sinan
author_sort Guclu, Metin
collection PubMed
description AIM: In the present study, we investigated the long-term effects of exenatide treatment on serum fasting ghrelin levels in patients with type 2 diabetes mellitus. METHODS: Type 2 diabetic patients, who were using metformin with and without the other antihyperglycemic drugs on a stable dose for at least 3 months, were enrolled in the study. BMI>35 kg/m(2) and HbA1c>7.0% were the additional inclusion criteria. Oral antihyperglycemic drugs, other than metformin, were stopped, and metformin treatment was continued at 2000 mg per day. Exenatide treatment was initiated at 5 µg per dose subcutaneously (sc) twice daily, and after one month, the dose of exenatide was increased to 10 µg twice daily. Changes in anthropometric variables, glycemic control, lipid parameters and total ghrelin levels were evaluated at baseline and following 12 weeks of treatment. RESULTS: Thirty-eight patients (male/female = 7/31) entered the study. The mean age of patients was 50.5 ± 8.8 years with a mean diabetes duration of 8.5 ± 4.9 years. The mean BMI was 41.6 ± 6.3 kg/m(2) and the mean HbA1c of patients was 8.9 ± 1.4%. The mean change in the weight of patients was −5.6 kg and the percentage change in weight was −5.2 ± 3.7% following 12 weeks of treatment. BMI, fasting plasma glucose and HbA1c levels of patients were decreased significantly (P < 0.001 and P < 0.001; respectively), while there was no change in lipid parameters. Serum fasting ghrelin levels were significantly suppressed following 12 weeks of exenatide treatment compared with baseline values (328.4 ± 166.8 vs 245.3 ± 164.8 pg/mL) (P = 0.024). CONCLUSION: These results suggest that the effects of exenatide on weight loss may be related with the suppression of serum fasting ghrelin levels, which is an orexigenic peptide.
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spelling pubmed-57766662018-01-24 Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus Guclu, Metin Kiyici, Sinem Gul, Zulfiye Cavun, Sinan Endocr Connect Research AIM: In the present study, we investigated the long-term effects of exenatide treatment on serum fasting ghrelin levels in patients with type 2 diabetes mellitus. METHODS: Type 2 diabetic patients, who were using metformin with and without the other antihyperglycemic drugs on a stable dose for at least 3 months, were enrolled in the study. BMI>35 kg/m(2) and HbA1c>7.0% were the additional inclusion criteria. Oral antihyperglycemic drugs, other than metformin, were stopped, and metformin treatment was continued at 2000 mg per day. Exenatide treatment was initiated at 5 µg per dose subcutaneously (sc) twice daily, and after one month, the dose of exenatide was increased to 10 µg twice daily. Changes in anthropometric variables, glycemic control, lipid parameters and total ghrelin levels were evaluated at baseline and following 12 weeks of treatment. RESULTS: Thirty-eight patients (male/female = 7/31) entered the study. The mean age of patients was 50.5 ± 8.8 years with a mean diabetes duration of 8.5 ± 4.9 years. The mean BMI was 41.6 ± 6.3 kg/m(2) and the mean HbA1c of patients was 8.9 ± 1.4%. The mean change in the weight of patients was −5.6 kg and the percentage change in weight was −5.2 ± 3.7% following 12 weeks of treatment. BMI, fasting plasma glucose and HbA1c levels of patients were decreased significantly (P < 0.001 and P < 0.001; respectively), while there was no change in lipid parameters. Serum fasting ghrelin levels were significantly suppressed following 12 weeks of exenatide treatment compared with baseline values (328.4 ± 166.8 vs 245.3 ± 164.8 pg/mL) (P = 0.024). CONCLUSION: These results suggest that the effects of exenatide on weight loss may be related with the suppression of serum fasting ghrelin levels, which is an orexigenic peptide. Bioscientifica Ltd 2017-12-07 /pmc/articles/PMC5776666/ /pubmed/29217653 http://dx.doi.org/10.1530/EC-17-0242 Text en © 2018 The authors http://creativecommons.org/licenses/by-nc/4.0/ This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Research
Guclu, Metin
Kiyici, Sinem
Gul, Zulfiye
Cavun, Sinan
Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus
title Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus
title_full Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus
title_fullStr Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus
title_full_unstemmed Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus
title_short Exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus
title_sort exenatide treatment causes suppression of serum fasting ghrelin levels in patients with type 2 diabetes mellitus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5776666/
https://www.ncbi.nlm.nih.gov/pubmed/29217653
http://dx.doi.org/10.1530/EC-17-0242
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