Association of Thrombomodulin Gene Polymorphism (C1418T) With Coronary Artery Disease in Pakistani Population

Authors

  • Muhammad Akbar Mughal
  • Muhammad Saleh Soomro
  • Syed Muhammad Ashraf Jahangeer AlSaani
  • Saba Shahid
  • Shariq Ahmed

DOI:

https://doi.org/10.12669/pjms.343.14864

Keywords:

Thrombomodulin (TM), Genetic polymorphism, C1418T, Coronary Artery Disease (CAD).

Abstract

Objectives: To find out the association between Thrombomodulin gene polymorphism (C1418T) with coronary artery disease in population of Karachi, Pakistan.

Methods: This case-control study was conducted in Tabba Heart Institute in collaboration with the National Institute of Blood Diseases, Karachi. We compared C/T dimorphism in 92 cases with 90 control subjects by allele-specific amplification. The results of PCR were confirmed by Gene sequencing. All the laboratory methods were strictly in compliance with the international standards. All variables that were either statistically significant in the univariate analyses or potentially important with respect to prevention or biologically relevant variables were included in logistic-regression analyses. Potential confounding was assessed with the use of multivariate models adjusted for participant

Author Biography

Muhammad Akbar Mughal

Department of Physiology

Associate Professor (officiating)

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Published

2018-06-12

How to Cite

Mughal, M. A., Soomro, M. S., Jahangeer AlSaani, S. M. A., Shahid, S., & Ahmed, S. (2018). Association of Thrombomodulin Gene Polymorphism (C1418T) With Coronary Artery Disease in Pakistani Population. Pakistan Journal of Medical Sciences, 34(3). https://doi.org/10.12669/pjms.343.14864

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Section

Original Articles