Volume 11, Issue 3 (Autumn 2014)                   bloodj 2014, 11(3): 207-213 | Back to browse issues page

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  Abstract

 Background and Objectives

 Arterial thrombosis, with MI as the severe complication, represents the most frequent cause of death in the world. Although there is no doubt that genetic factors contribute significantly to the prothrombotic state, the data on polymorphisms in candidate genes are still inconclusive. We investigated if T13254C polymorphism in the platelet GPVI gene confers an increased risk of premature acute myocardial infarction (MI).

 Materials and Methods

 We conducted a case-control study of 100 young males with premature acute MI and 100 inpatient controls of the similar age, without any known heart diseases. Genotyping was done using PCR-RFLP. The significance of differences between cases and controls with respect to the variables was tested using student’s t test and Chi square. Logical regression model was used to control confounding variables.

  

 Results

 The allele frequencies of T13254C polymorphism did not differ between patients (30%) and controls (33%), and this polymorphism was not associated with premature acute MI (p < 0.05). Logistic regression analysis also indicated no association between these polymorphisms and premature MI.

 Conclusions

 Compatible with our study, the T13254C polymorphism of platelet collagen receptor did not play a significant role in the development of premature MI.

  

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Type of Study: Research | Subject: Hematology

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