Objectives: Inflammation caused by adipokines such as adiponectin, leptin, resistin, visfatin, interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) released by fat cells and immune cells within fat tissue is a significant factor in the onset of insulin resistance and Type 2 diabetes mellitus (T2DM). This study explores the relationship among these adipokines and insulin resistance in T2DM patients, focusing on the impact of abdominal obesity.
Methods: The study involved 73 adult T2DM patients who were seperated into two groups based on their body mass index (BMI): 47 were classified as obese (BMI ≥30 kg/m²), and 26 were classified as non-obese (BMI <25 kg/m²). Additionally, 42 healthy controls were included, comprising 18 obese and 24 non-obese individuals. Adipokine concentrations (resistin, leptin, adiponectin, visfatin, IL-6 and TNF-α) were measured with the ELISA method.
Results: The concentrations of adiponectin were substantially lower in T2DM patients relative to the control group (P<0.0125). Leptin concentrations did not show significant differences between the groups, but there was a notable increase in obese controls compared to non-obese controls (P<0.0125). TNF-α concentrations were significantly higher in obese controls than in non-obese controls (P<0.001). Resistin concentrations were significantly correlated with C-reactive protein (CRP) and IL-6 in both groups, independent of BMI (P=0.001 and P<0.0125, respectively). We found that CRP levels were significantly higher in both obese diabetics compared to non-obese diabetics and in obese controls compared to non-obese controls (P<0.0001).
Conclusions: Adipose tissue is a crucial determinant of circulating inflammation markers. Elevated CRP concentrations in obesity may result from insulin resistance rather than being a cause. Further research is required to comprehend the connection between fatty tissue, insulin resistance, and elevated inflammatory markers.
This study follows the principles of the Declaration of Helsinki. The study was conducted with approval from Istanbul University Faculty of Medicine Clinical Research Ethics Committee dated 28.08.2006 and numbered 1745. All participants provided their informed consent.
Primary Language | English |
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Subjects | Clinical Chemistry |
Journal Section | Original Articles |
Authors | |
Early Pub Date | February 11, 2025 |
Publication Date | |
Submission Date | August 23, 2024 |
Acceptance Date | November 8, 2024 |
Published in Issue | Year 2025 EARLY ONLINE |