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Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients
OBJECTIVES: To compare the anti-inflammatory effect of sitagliptin and glimepiride by measuring CRP in overweight Type-2 diabetic patients. METHODS: This clinical trial was conducted at diabetic clinic of Islam Central Hospital, Sialkot over a period of six months from June to November 2017. A total...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Professional Medical Publications
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500845/ https://www.ncbi.nlm.nih.gov/pubmed/31086519 http://dx.doi.org/10.12669/pjms.35.2.645 |
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author | Hussain, Mazhar Rafique, Muhammad Aamir Iqbal, Javed Akhtar, Lubna |
author_facet | Hussain, Mazhar Rafique, Muhammad Aamir Iqbal, Javed Akhtar, Lubna |
author_sort | Hussain, Mazhar |
collection | PubMed |
description | OBJECTIVES: To compare the anti-inflammatory effect of sitagliptin and glimepiride by measuring CRP in overweight Type-2 diabetic patients. METHODS: This clinical trial was conducted at diabetic clinic of Islam Central Hospital, Sialkot over a period of six months from June to November 2017. A total of 110 overweight Type-2 diabetic patients were divided in to two groups. Group-A was given tablet sitagliptin 50mg while Group-B was given tablet glimepiride 2mg for a period of 12 weeks. The dose was titrated according to blood sugar level. The primary outcome was measuring changes in CRP while secondary outcomes was changes in BMI, blood sugar, HbA1C, lipid profile and CRP from baseline in both study group using SPSS 16. RESULTS: After 12 weeks treatment, body weight increased in glimepiride but slightly reduced in sitagliptin, however comparison between them was non significant (p=0.07). Although both groups reduced blood sugar and HbA1c but comparison between them was non significant (p=0.59 and p=0.17 respectively) value. However lipid profile improved significantly in sitagliptin vs. glimepiride group i.e total cholesterol (-25±32.5 vs +1.5±45.4 P=0.02) triglycerides (-19±44.6 vs-1.8±48.7 P=0.001) LDL- cholesterol (-10±22.4 vs-0.8±18.7 P=0.001) HDL-cholesterol (-2.6±6.2 vs 1.2±5.2 P=0.03).Sitagliptin significantly reduced CRP in comparison to glimepiride (-2.3±1.8 vs0.8±1.5 P=0.001). CONCLUSION: Sitagliptin has strong anti inflammatory effect marked by reduction in CRP level in comparison to glimepiride in overweight type-2 diabetic patients. It also exerted beneficial effect on glycemic and lipid profiles. |
format | Online Article Text |
id | pubmed-6500845 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Professional Medical Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-65008452019-05-13 Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients Hussain, Mazhar Rafique, Muhammad Aamir Iqbal, Javed Akhtar, Lubna Pak J Med Sci Original Article OBJECTIVES: To compare the anti-inflammatory effect of sitagliptin and glimepiride by measuring CRP in overweight Type-2 diabetic patients. METHODS: This clinical trial was conducted at diabetic clinic of Islam Central Hospital, Sialkot over a period of six months from June to November 2017. A total of 110 overweight Type-2 diabetic patients were divided in to two groups. Group-A was given tablet sitagliptin 50mg while Group-B was given tablet glimepiride 2mg for a period of 12 weeks. The dose was titrated according to blood sugar level. The primary outcome was measuring changes in CRP while secondary outcomes was changes in BMI, blood sugar, HbA1C, lipid profile and CRP from baseline in both study group using SPSS 16. RESULTS: After 12 weeks treatment, body weight increased in glimepiride but slightly reduced in sitagliptin, however comparison between them was non significant (p=0.07). Although both groups reduced blood sugar and HbA1c but comparison between them was non significant (p=0.59 and p=0.17 respectively) value. However lipid profile improved significantly in sitagliptin vs. glimepiride group i.e total cholesterol (-25±32.5 vs +1.5±45.4 P=0.02) triglycerides (-19±44.6 vs-1.8±48.7 P=0.001) LDL- cholesterol (-10±22.4 vs-0.8±18.7 P=0.001) HDL-cholesterol (-2.6±6.2 vs 1.2±5.2 P=0.03).Sitagliptin significantly reduced CRP in comparison to glimepiride (-2.3±1.8 vs0.8±1.5 P=0.001). CONCLUSION: Sitagliptin has strong anti inflammatory effect marked by reduction in CRP level in comparison to glimepiride in overweight type-2 diabetic patients. It also exerted beneficial effect on glycemic and lipid profiles. Professional Medical Publications 2019 /pmc/articles/PMC6500845/ /pubmed/31086519 http://dx.doi.org/10.12669/pjms.35.2.645 Text en Copyright: © Pakistan Journal of Medical Sciences http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hussain, Mazhar Rafique, Muhammad Aamir Iqbal, Javed Akhtar, Lubna Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients |
title | Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients |
title_full | Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients |
title_fullStr | Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients |
title_full_unstemmed | Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients |
title_short | Effect of sitagliptin and glimepiride on C-reactive protein (CRP) in overweight Type-2 diabetic patients |
title_sort | effect of sitagliptin and glimepiride on c-reactive protein (crp) in overweight type-2 diabetic patients |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500845/ https://www.ncbi.nlm.nih.gov/pubmed/31086519 http://dx.doi.org/10.12669/pjms.35.2.645 |
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