Comparison of Antidiabetic Medications during the Treatment of Atherosclerosis in T2DM Patients

Author:

Liu Xiaojie12ORCID,Mei Tao3,Chen Wei4,Ye Shandong15ORCID

Affiliation:

1. School of Medicine, Shandong University, Jinan, Shandong, China

2. Department of Geriatrics, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China

3. Department of MEC, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China

4. Department of Nephrology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China

5. Department of Endocrinology, Anhui Provincial Hospital Affiliated to Anhui Medical University, Hefei, China

Abstract

Type 2 diabetes is often associated with arterial atherosclerosis in large blood vessels. We set out to elucidate whether commonly used antidiabetic drugs metformin, sitagliptin, and pioglitazone will reduce atherosclerosis in T2DM patients. We enrolled 176 individuals with type 2 diabetes, which were divided into four treatment groups according to different oral drugs: metformin alone, sitagliptin alone, pioglitazone alone, or combination of metformin and sitagliptin. We assessed changes in glycometabolism, lipid metabolism, cytokine released, and carotid artery intima-media thickness as the readout for improvement in atherosclerosis. HbA1c levels were significantly decreased in all treatment groups (p<0.05), and FBG levels were also decreased in metformin and combined groups (p<0.05). In addition, we found IL-6 levels significantly decreased in all treatment groups (p<0.05). Treatment with pioglitazone showed a significant increase in BMI, HDL, and ADPN levels (p<0.05). We also observed a significant decrease in NHDL levels in the combined treatment group (p<0.05). Our data revealed that in addition to hypoglycemic properties of metformin, sitagliptin, and pioglitazone, these drugs also have the potential to promote an anti-inflammatory response. Therefore, combination therapy may be more beneficial for reducing atherosclerosis in patients with type 2 diabetes. The clinical trial is registered with ChiCTR-ORC-17010835.

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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