[Home ] [Archive]   [ فارسی ]  
:: Main :: About us :: Current Issue :: Archive :: Search :: Submit :: Contact ::
:: Volume 7, Issue 1 (Spring 2010) ::
Sci J Iran Blood Transfus Organ 2010, 7(1): 1-8 Back to browse issues page
Correlation of FXII 46CT polymorphism with FXII activity and risk of thrombotic diseases
P. Rasi Ghaemi, A. Kazemi , F. Ala, M. Jazebi, F. Razmkhah
Abstract:   (15003 Views)

  Abstract

 Background and Objectives

 There are a number of well-characterized genetic defects that lead to increased risk of thrombosis. Results from previous studies have indicated that plasma FXII activity levels are strongly determined by a 46CT polymorphism in the FXII gene. In the present study, the risk of thrombophilic diseases related to this polymorphism was investigated.

 

 Materials and Methods

 One hundred sixty individuals were included in this case-control study: 120 patients diagnosed with thrombophilia and 40 age-gender-matched controls. For each subject, FXII activity level was measured using a one-step clotting assay, and 46CT polymorphism was genotyped using a PCR-RFLP techniques.

 

 Results

 In this study, FXII activity < 68% was associated with an increased risk of thrombophilia with an adjusted odds ratio of 4.75 (CI 95% = 1.07 – 21.1). In CT and TT genotypes, the adjusted odds ratios were respectively 1.81 (CI 95% = 0.83-3.94) and 2.17 (CI 95% = 0.45-10.7) for thrombotic patients compared with the controls. Thus, we did not find any association of the mutated T allele in the heterozygous or homozygous state with an increased risk of thrombophilia.

 

 Conclusions

 This study showed that 46CT is a strong determinant of FXII activity. However, there was not any association between mutant T allele and increased risk of thrombosis. Therefore, it was speculated that reduced FXII activity is not the cause but the outcome of thrombosis. In other words, lower FXII activity is not a risk factor for thrombosis, rather it simply represents a risk marker.

 

 Key words : Thrombosis, polymorphism (Genetic), Odds Ratio 

 

Keywords: Thrombosis, polymorphism (Genetic), Odds Ratio
Full-Text [PDF 280 kb]   (2141 Downloads)    
Type of Study: Research | Subject: Hematology
Published: 2014/07/23
Send email to the article author

Add your comments about this article
Your username or Email:

CAPTCHA


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Rasi Ghaemi P, Kazemi A, Ala F, Jazebi M, Razmkhah F. Correlation of FXII 46CT polymorphism with FXII activity and risk of thrombotic diseases. Sci J Iran Blood Transfus Organ. 2010; 7 (1) :1-8
URL: http://bloodjournal.ir/article-1-378-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 7, Issue 1 (Spring 2010) Back to browse issues page
فصلنامه پژوهشی خون Scientific Journal of Iran Blood Transfus Organ
The Scientific Journal of Iranian Blood Transfusion Organization - Copyright 2006 by IBTO
Persian site map - English site map - Created in 0.07 seconds with 31 queries by YEKTAWEB 4341