Abstract
Aims
Increasing evidence has shown that selenoprotein P levels are elevated in type 2 diabetes mellitus and are associated with insulin resistance and release. This study aimed to determine if there was a connection between selenoprotein P levels and metabolic parameters in patients with diabetes with microvascular complications.
Methods
Serum selenoprotein P concentrations were measured by ELISA in 44 patients with diabetes with complications and 36 patients with diabetes without complications.
Results
There was no statistically significant difference in selenoprotein P levels between the groups [1.9 (0.9–2.6) and 1.9 (0.8–2.4) ng/mL, respectively, p = 0.565]. Selenoprotein P, glucose, glycosylated hemoglobin, C-reactive protein, triglycerides, total cholesterol, and low-density lipoprotein cholesterol levels were not statistically significantly correlated in patients with complications. However, there was a significant correlation with high-density lipoprotein cholesterol (r = − 0.401, p = 0.042).
Conclusions
We did not find high selenoprotein P levels in patients with complications, but its inverse association with high-density lipoprotein cholesterol indicates that it may play a role in developing cardiovascular disease in this community of patients.
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Data Availability
The data that support the findings of this study are available on request from the corresponding author.
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Acknowledgements
The authors would like to thank the Scientific Research Projects Unit of Kırşehir Ahi Evran University.
Funding
This study was supported by Kırsehir Ahi Evran University Scientific Research Projects Unit.
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Kırsehir Ahi Evran University Faculty of Medicine approved the study of Medicine Ethics Committee (approval date and number: 2020-04/31). The procedures used in this study adhere to the tenets of the Declaration of Helsinki.
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Ilanbey, B., Yücel, H.E., Uçar, C. et al. Selenoprotein P levels in patients with diabetes mellitus with complications. Int J Diabetes Dev Ctries 42, 735–740 (2022). https://doi.org/10.1007/s13410-021-01029-0
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DOI: https://doi.org/10.1007/s13410-021-01029-0