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The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial

Systemic inflammation and oxidative burden in patients with type 2 diabetes mellitus (T2DM) causes deleterious cardiovascular outcomes. We sought to investigate the clinical antioxidative and anti-inflammatory effects of empagliflozin. Platelet function, oxidant and antioxidant biomarkers and pro-in...

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Autores principales: Gohari, Sepehr, Reshadmanesh, Tara, Khodabandehloo, Hadi, Karbalaee-Hasani, Amir, Ahangar, Hassan, Arsang-Jang, Shahram, Ismail-Beigi, Faramarz, Dadashi, Mohsen, Ghanbari, Samin, Taheri, Homa, Fathi, Mojtaba, Muhammadi, Muhammad Javad, Mahmoodian, Reyhaneh, Asgari, Atieh, Tayaranian, Mohammadreza, Moharrami, Mehdi, Mahjani, Mahsa, Ghobadian, Bijan, Chiti, Hossein, Gohari, Sheida
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669535/
https://www.ncbi.nlm.nih.gov/pubmed/36397128
http://dx.doi.org/10.1186/s13098-022-00951-5
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author Gohari, Sepehr
Reshadmanesh, Tara
Khodabandehloo, Hadi
Karbalaee-Hasani, Amir
Ahangar, Hassan
Arsang-Jang, Shahram
Ismail-Beigi, Faramarz
Dadashi, Mohsen
Ghanbari, Samin
Taheri, Homa
Fathi, Mojtaba
Muhammadi, Muhammad Javad
Mahmoodian, Reyhaneh
Asgari, Atieh
Tayaranian, Mohammadreza
Moharrami, Mehdi
Mahjani, Mahsa
Ghobadian, Bijan
Chiti, Hossein
Gohari, Sheida
author_facet Gohari, Sepehr
Reshadmanesh, Tara
Khodabandehloo, Hadi
Karbalaee-Hasani, Amir
Ahangar, Hassan
Arsang-Jang, Shahram
Ismail-Beigi, Faramarz
Dadashi, Mohsen
Ghanbari, Samin
Taheri, Homa
Fathi, Mojtaba
Muhammadi, Muhammad Javad
Mahmoodian, Reyhaneh
Asgari, Atieh
Tayaranian, Mohammadreza
Moharrami, Mehdi
Mahjani, Mahsa
Ghobadian, Bijan
Chiti, Hossein
Gohari, Sheida
author_sort Gohari, Sepehr
collection PubMed
description Systemic inflammation and oxidative burden in patients with type 2 diabetes mellitus (T2DM) causes deleterious cardiovascular outcomes. We sought to investigate the clinical antioxidative and anti-inflammatory effects of empagliflozin. Platelet function, oxidant and antioxidant biomarkers and pro-inflammatory agents at baseline and at 26 weeks were measured. A total of 95 patients (41.05% male, mean age 62.85 ± 7.91 years, mean HbA(1c) 7.89 ± 0.96%) with concomitant T2DM and coronary artery disease (CAD) were randomized (1:1) to receive empagliflozin (10 mg/daily) or placebo. Patients treated with empagliflozin had lower levels of interleukin 6 (IL-6) (adjusted difference (adiff): − 1.06 pg/mL, 95% CI − 1.80; − 0.32, P = 0.006), interleukin 1β (IL-1β) and high-sensitive C-reactive protein (Hs-CRP) (adiff: − 4.58 pg/mL and − 2.86 mg/L; P = 0.32 and 0.003, respectively) compared to placebo. There were elevations in super oxidase dismutase (SOD) activity, glutathione (GSHr), and total antioxidant capacity (TAC) with empagliflozin (adiff: 3.7 U/mL, 0.57 muM, and 124.08 mmol/L, 95% CI 1.36; 6.05, 0.19; 0.95, and 47.98; 200.18, P = 0.002, 0.004, and 0.002, respectively). While reactive oxygen species (ROS) improved significantly (adiff: − 342.51, 95% CI − 474.23; − 210.79, P < 0.001), the changes in catalase activity (CAT), malondialdehyde (MDA), or protein carbonyl groups (PCG) were not significant. Moreover, the P-selectin antigen expression on platelet surface was significantly reduced (adiff: − 8.81, 95% CI − 14.87; − 2.75, P = 0.005). Markers of glycemic status (fasting blood glucose, HbA(1c), and HOMA-IR (homeostatic model assessment for insulin resistance) significantly improved (P < 0.001). Among patients with T2DM and CAD, 6-month treatment with empagliflozin can mitigate inflammation, platelet activity and oxidative stress and is associated with clinical cardiovascular benefits. Trial Registration Iranian Registry of Clinical Trials. www.IRCT.ir, Identifier: IRCT20190412043247N2. Registration Date: 6/13/2020. Registration timing: prospective SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-022-00951-5.
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spelling pubmed-96695352022-11-18 The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial Gohari, Sepehr Reshadmanesh, Tara Khodabandehloo, Hadi Karbalaee-Hasani, Amir Ahangar, Hassan Arsang-Jang, Shahram Ismail-Beigi, Faramarz Dadashi, Mohsen Ghanbari, Samin Taheri, Homa Fathi, Mojtaba Muhammadi, Muhammad Javad Mahmoodian, Reyhaneh Asgari, Atieh Tayaranian, Mohammadreza Moharrami, Mehdi Mahjani, Mahsa Ghobadian, Bijan Chiti, Hossein Gohari, Sheida Diabetol Metab Syndr Research Systemic inflammation and oxidative burden in patients with type 2 diabetes mellitus (T2DM) causes deleterious cardiovascular outcomes. We sought to investigate the clinical antioxidative and anti-inflammatory effects of empagliflozin. Platelet function, oxidant and antioxidant biomarkers and pro-inflammatory agents at baseline and at 26 weeks were measured. A total of 95 patients (41.05% male, mean age 62.85 ± 7.91 years, mean HbA(1c) 7.89 ± 0.96%) with concomitant T2DM and coronary artery disease (CAD) were randomized (1:1) to receive empagliflozin (10 mg/daily) or placebo. Patients treated with empagliflozin had lower levels of interleukin 6 (IL-6) (adjusted difference (adiff): − 1.06 pg/mL, 95% CI − 1.80; − 0.32, P = 0.006), interleukin 1β (IL-1β) and high-sensitive C-reactive protein (Hs-CRP) (adiff: − 4.58 pg/mL and − 2.86 mg/L; P = 0.32 and 0.003, respectively) compared to placebo. There were elevations in super oxidase dismutase (SOD) activity, glutathione (GSHr), and total antioxidant capacity (TAC) with empagliflozin (adiff: 3.7 U/mL, 0.57 muM, and 124.08 mmol/L, 95% CI 1.36; 6.05, 0.19; 0.95, and 47.98; 200.18, P = 0.002, 0.004, and 0.002, respectively). While reactive oxygen species (ROS) improved significantly (adiff: − 342.51, 95% CI − 474.23; − 210.79, P < 0.001), the changes in catalase activity (CAT), malondialdehyde (MDA), or protein carbonyl groups (PCG) were not significant. Moreover, the P-selectin antigen expression on platelet surface was significantly reduced (adiff: − 8.81, 95% CI − 14.87; − 2.75, P = 0.005). Markers of glycemic status (fasting blood glucose, HbA(1c), and HOMA-IR (homeostatic model assessment for insulin resistance) significantly improved (P < 0.001). Among patients with T2DM and CAD, 6-month treatment with empagliflozin can mitigate inflammation, platelet activity and oxidative stress and is associated with clinical cardiovascular benefits. Trial Registration Iranian Registry of Clinical Trials. www.IRCT.ir, Identifier: IRCT20190412043247N2. Registration Date: 6/13/2020. Registration timing: prospective SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-022-00951-5. BioMed Central 2022-11-17 /pmc/articles/PMC9669535/ /pubmed/36397128 http://dx.doi.org/10.1186/s13098-022-00951-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Gohari, Sepehr
Reshadmanesh, Tara
Khodabandehloo, Hadi
Karbalaee-Hasani, Amir
Ahangar, Hassan
Arsang-Jang, Shahram
Ismail-Beigi, Faramarz
Dadashi, Mohsen
Ghanbari, Samin
Taheri, Homa
Fathi, Mojtaba
Muhammadi, Muhammad Javad
Mahmoodian, Reyhaneh
Asgari, Atieh
Tayaranian, Mohammadreza
Moharrami, Mehdi
Mahjani, Mahsa
Ghobadian, Bijan
Chiti, Hossein
Gohari, Sheida
The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial
title The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial
title_full The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial
title_fullStr The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial
title_full_unstemmed The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial
title_short The effect of EMPAgliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and Coronary ARtery Disease: the EMPA-CARD randomized controlled trial
title_sort effect of empagliflozin on markers of inflammation in patients with concomitant type 2 diabetes mellitus and coronary artery disease: the empa-card randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9669535/
https://www.ncbi.nlm.nih.gov/pubmed/36397128
http://dx.doi.org/10.1186/s13098-022-00951-5
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