Transcription Factor 7/Like2 (TCF7/L2) Gene Associated With Metabolic Syndrome In The Type 2 Diabetes

Authors

  • Shazia Azhar Baqai Institute of Medical Technology, Baqai Medical University, Karachi
  • Faiza Agha Liaquat National Hospital and Medical College, Karachi
  • Naheed Akhtar Karachi Institute of Medical Sciences, CMH Malir Cantt, Karachi
  • Sara Fatima Baqai Dental College, Baqai Medical University, Karachi
  • Nasir Jamil Liaquat College of Medicine and Dentistry, Darul Sehat Hospital, Karachi, Pakistan.
  • Nadia Naeem Jinnah Sindh Medical University, Karachi

DOI:

https://doi.org/10.36283/ziun-pjmd15-1/008

Keywords:

TCF7L2 (Transcription factor 7 L2), Proliferative diabetic retinopathy

Abstract

Background: Diabetic retinopathy (DR) is a chronic complication of diabetes mellitus which can be due to micro vascular changes occurring in retina due to hyperglycemia. Polymorphism in gene TCF7L2 rs7903146 has been shown to increase susceptibility to developing diabetes mellitus.

Aim: Association between Diabetic retinopathy (DR) and polymorphism of TCF7L2 expression and alteration in VEGF expression level has also been found in Type2 DM.

Method: A comparative research was carried out in the Department of Biochemistry, with 148 volunteers aged 18 to 50 recruited from the Baqai Institute of Diabetology and Endocrinology (BIDE). Clinical data, anthropometric measures, and biochemical markers such FBS, OGTT, HbA1c, and lipid profile were obtained. Genomic DNA was collected, and the TCF7L2 gene polymorphism (rs7903146) was examined by Sanger sequencing.

Results: The study analyzed 148 Type 2 Diabetes mellitus (T2DM) patients with and without retinopathy, with a mean age of 43.27±9.45 years. Results showed significant differences in blood pressure, fasting blood glucose, HbA1c, triglycerides, and cholesterol levels between groups. The TT genotype was more abundant in group B, while the CT genotype was higher in group A. The majority of T2DM patients with retinopathy had complications like retinal hemorrhages, microdot, and blindness.

Conclusion: Overall, the homozygous TT genotype of TCF7L2 rs7903146 polymorphism was found dominant in T2DM subjects with retinopathy as compared with T2DM without retinopathy, and CT genotype was found higher in T2DM subjects without retinopathy and healthy individuals. We also found mutant T allele was predominantly higher in T2DM subjects with and without retinopathy.

Author Biographies

  • Shazia Azhar, Baqai Institute of Medical Technology, Baqai Medical University, Karachi

    Department of Medical Technology

  • Faiza Agha, Liaquat National Hospital and Medical College, Karachi

    Department of Biochemistry

  • Naheed Akhtar , Karachi Institute of Medical Sciences, CMH Malir Cantt, Karachi

    Department of Anatomy

  • Sara Fatima , Baqai Dental College, Baqai Medical University, Karachi

    Department of Oral Medicine

  • Nasir Jamil, Liaquat College of Medicine and Dentistry, Darul Sehat Hospital, Karachi, Pakistan.

    Department of Medicine

  • Nadia Naeem, Jinnah Sindh Medical University, Karachi

    Department of Pharmacology

References

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Published

2026-01-14

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How to Cite

1.
Azhar S, Agha F, Akhtar N, Fatima S, Nasir Jamil NJ, Naeem N. Transcription Factor 7/Like2 (TCF7/L2) Gene Associated With Metabolic Syndrome In The Type 2 Diabetes. PJMD [Internet]. 2026 Jan. 14 [cited 2026 Jun. 4];15(1). Available from: https://ojs.zu.edu.pk/pjmd/article/view/4167

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