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Correlation between TCF7L2 gene expression and certain biochemical parameters in type 2 diabetes mellitus
Alaa H Younus1,2, Abdul Hussein M Al-Faisal2
1Biomedical Engineering Department, University of Technology, Iraq.
Journal of Taibah University Medical Sciences
|May 13, 2024
Summary
The TCF7L2 gene expression is higher in older type 2 diabetes mellitus (T2DM) patients, potentially impacting insulin secretion. This study examined TCF7L2 gene expression and biochemical markers in Iraqi T2DM patients.
Area of Science:
- Genetics and Molecular Biology
- Endocrinology and Metabolism
- Population Health
Background:
- The transcription factor 7-like 2 (TCF7L2) gene is implicated in type 2 diabetes mellitus (T2DM) predisposition across diverse ethnic groups.
- Understanding TCF7L2 gene expression variations in relation to age and metabolic profiles is crucial for T2DM management.
Purpose of the Study:
- To investigate the relationship between TCF7L2 gene expression and key biochemical indices in different age categories of T2DM patients.
- To analyze TCF7L2 gene expression differences between young and old T2DM individuals within the Iraqi population.
Main Methods:
- Quantitative PCR (qPCR) was employed to measure TCF7L2 gene expression.
- Biochemical parameters including HbA1c, triglyceride (TG), LDL, and HDL levels were assessed.
- Body Mass Index (BMI) was calculated, and data were statistically analyzed for 150 participants across young T2DM, old T2DM, and healthy control groups.
Main Results:
- T2DM patients exhibited higher BMI, TG, and LDL, with lower HDL compared to controls.
- Significant correlations were observed between HbA1c and BMI, TG, LDL, and HDL levels.
- TCF7L2 gene expression was significantly higher in old T2DM patients (1.68-fold) compared to young T2DM patients (0.207-fold).
Conclusions:
- Age significantly influences TCF7L2 gene expression in T2DM patients, with older individuals showing elevated levels.
- The observed age-related increase in TCF7L2 expression may have implications for beta-cell function and insulin secretion in T2DM.
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