The Association between Leptin and Asprosin Levels in Female Patients with Type II Diabetes Mellitus
DOI:
https://doi.org/10.32007/jfacmedbaghdad.6632346Keywords:
Asprosin, Fasting Blood Glucose, Glycated hemoglobin, Leptin, Type II diabetes mellitusAbstract
Background: Leptin and asprosin are adipokines secreted by white adipose tissue. The leptin and asprosin molecules have many functions in the central nervous system and other functions of the body: Appetite, glucose metabolism, insulin resistance, and cellular death.
Objectives: The study aims to determine the potential relationship between leptin and asprosin hormones in female patients with type II diabetes mellitus.
Methods: The present study was conducted in Al-Mahmodia Hospital / Baghdad and the laboratories of the College of Science for Girls / University of Baghdad / Iraq, for the period from 1/11/2023 to 1/2/ 2024. This study is a comparative analysis of several essential biomarkers found in the sera of individuals with diabetes via estimating leptin, asprosin, fasting blood glucose, glycated hemoglobin, body mass index, total cholesterol, triglycerides, high-density lipoprotein, low-density lipoprotein, aspartate aminotransferase, alanine aminotransferase and alkaline phosphatase in females with type II diabetes mellitus. The study consisted of 60 participants grouped into: Group I (30 females with diabetes), and group II (30 healthy females). The Biochemical parameters of every participant were ascertained. The quantification of leptin and asprosin in the serum was conducted using the enzyme-linked immunosorbent assay (ELISA).
Results: The levels of leptin and asprosin were markedly high in the diabetic group [(5.1 ± 0.69), and (10.3 ± 1.07)] compared with the control group [(2.0 ± 0.48), and (1.6 ± 0.16)] respectively, with a significant difference.
Conclusion: Despite the high levels of leptin and asprosin in female patients with Type II diabetes mellitus, the relationship between leptin and asprosin was a weak negative one.
Received: April, 2024
Revised: June,2024
Accepted: July, 2024
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