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Renoprotective Potency of Sitagliptin versus Pioglitazone in Type 2 Diabetic Patients: Impact on LncMIAT
[Image: see text] Background: Diabetes mellitus (DM) represents one of the most important reasons for chronic kidney diseases due to the high level of blood glucose that destructs blood vessels. Objective: The present study focused on investigating the protective impact of sitagliptin on kidney comp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652733/ https://www.ncbi.nlm.nih.gov/pubmed/38024775 http://dx.doi.org/10.1021/acsomega.3c07008 |
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author | Kandeil, Mohamed A. Shaarawy, Mohamed A. Mourad, Hamdy A. Mahmoud, Mohamed O. |
author_facet | Kandeil, Mohamed A. Shaarawy, Mohamed A. Mourad, Hamdy A. Mahmoud, Mohamed O. |
author_sort | Kandeil, Mohamed A. |
collection | PubMed |
description | [Image: see text] Background: Diabetes mellitus (DM) represents one of the most important reasons for chronic kidney diseases due to the high level of blood glucose that destructs blood vessels. Objective: The present study focused on investigating the protective impact of sitagliptin on kidney complication in type 2 diabetes mellitus (T2DM) patients in comparison to pioglitazone to examine which has the superior effect against the nephritic complication of DM. Methods: Eighty adult subjects were classified into four groups: control group, pioglitazone-treated T2DM patients (P group), sitagliptin-treated T2DM patients for less than one year (SL group), and sitagliptin-treated T2DM patients for more than one year (SM group). Blood samples were withdrawn from all subjects for analysis of neutrophil gelatinase-associated lipocalin (NGAL), vanin-1, kidney injury molecule-1 (KIM-1), glyoxalase-1 (Glo-1), methylglyoxal (MG), cystatin-C, and interleukin-18 (IL-18) using competitive ELISA kits. Also, long noncoding myocardial infarction associated transcript (lncMIAT) was measured in whole blood using qRT-PCR. Results: The present study revealed that the lncMIAT expression level was significantly higher in the P group as compared to the SL group, SM group, or healthy control group. Additionally, serum NGAL, vanin-1, KIM-1, Glo-1, MG, and cystatin-C were significantly higher in the P group and SL group as compared to the SM group and healthy control group. Conclusion: Sitagliptin protected the kidney through downregulation of lncMIAT besides amelioration of kidney injury marker levels, which was more preferable than in pioglitazone therapy. |
format | Online Article Text |
id | pubmed-10652733 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106527332023-11-03 Renoprotective Potency of Sitagliptin versus Pioglitazone in Type 2 Diabetic Patients: Impact on LncMIAT Kandeil, Mohamed A. Shaarawy, Mohamed A. Mourad, Hamdy A. Mahmoud, Mohamed O. ACS Omega [Image: see text] Background: Diabetes mellitus (DM) represents one of the most important reasons for chronic kidney diseases due to the high level of blood glucose that destructs blood vessels. Objective: The present study focused on investigating the protective impact of sitagliptin on kidney complication in type 2 diabetes mellitus (T2DM) patients in comparison to pioglitazone to examine which has the superior effect against the nephritic complication of DM. Methods: Eighty adult subjects were classified into four groups: control group, pioglitazone-treated T2DM patients (P group), sitagliptin-treated T2DM patients for less than one year (SL group), and sitagliptin-treated T2DM patients for more than one year (SM group). Blood samples were withdrawn from all subjects for analysis of neutrophil gelatinase-associated lipocalin (NGAL), vanin-1, kidney injury molecule-1 (KIM-1), glyoxalase-1 (Glo-1), methylglyoxal (MG), cystatin-C, and interleukin-18 (IL-18) using competitive ELISA kits. Also, long noncoding myocardial infarction associated transcript (lncMIAT) was measured in whole blood using qRT-PCR. Results: The present study revealed that the lncMIAT expression level was significantly higher in the P group as compared to the SL group, SM group, or healthy control group. Additionally, serum NGAL, vanin-1, KIM-1, Glo-1, MG, and cystatin-C were significantly higher in the P group and SL group as compared to the SM group and healthy control group. Conclusion: Sitagliptin protected the kidney through downregulation of lncMIAT besides amelioration of kidney injury marker levels, which was more preferable than in pioglitazone therapy. American Chemical Society 2023-11-03 /pmc/articles/PMC10652733/ /pubmed/38024775 http://dx.doi.org/10.1021/acsomega.3c07008 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Kandeil, Mohamed A. Shaarawy, Mohamed A. Mourad, Hamdy A. Mahmoud, Mohamed O. Renoprotective Potency of Sitagliptin versus Pioglitazone in Type 2 Diabetic Patients: Impact on LncMIAT |
title | Renoprotective Potency of Sitagliptin versus Pioglitazone
in Type 2 Diabetic Patients: Impact on LncMIAT |
title_full | Renoprotective Potency of Sitagliptin versus Pioglitazone
in Type 2 Diabetic Patients: Impact on LncMIAT |
title_fullStr | Renoprotective Potency of Sitagliptin versus Pioglitazone
in Type 2 Diabetic Patients: Impact on LncMIAT |
title_full_unstemmed | Renoprotective Potency of Sitagliptin versus Pioglitazone
in Type 2 Diabetic Patients: Impact on LncMIAT |
title_short | Renoprotective Potency of Sitagliptin versus Pioglitazone
in Type 2 Diabetic Patients: Impact on LncMIAT |
title_sort | renoprotective potency of sitagliptin versus pioglitazone
in type 2 diabetic patients: impact on lncmiat |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652733/ https://www.ncbi.nlm.nih.gov/pubmed/38024775 http://dx.doi.org/10.1021/acsomega.3c07008 |
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