Abstract

The role of ABO gene polymorphisms in acute coronary syndrome (ACS) and lipid metabolism is increasingly recognized. We investigated whetherABO gene polymorphisms are significantly associated with ACS and the plasma lipid profile. SixABOgene polymorphisms (rs651007T/C, rs579459T/C, rs495928T/C, rs8176746T/G, rs8176740A/T, and rs512770T/C) were determined by 5'exonuclease TaqMan assays in 611 patients with ACS and 676 healthy controls. The results demonstrated that the rs8176746Tallele was associated with a lower risk of ACS under the co-dominant, dominant, recessive, over-dominant, and additive models (P= 0.0004,P= 0.0002,P= 0.039, P= 0.0009, andP= 0.0001, respectively). Furthermore, under co-dominant, dominant, and additive models, the rs8176740Aallele was associated with a lower risk of ACS(P= 0.041,P= 0.022, andP= 0.039, respectively). On the other hand, the rs579459Callele was associated with a lower risk of ACS under the dominant, over-dominant, and additive models (P= 0.025,P= 0.035, andP= 0.037, respectively). In a subanalysis performed with the control group, rs8176746Tand rs8176740Aalleles were associated with low systolic blood pressure and with both high high-density lipoprotein-cholesterol (HDL-C) and low triglyceride plasma concentrations, respectively. In conclusion, ABOgene polymorphisms were associated with a lower risk of ACS, and lower systolic blood pressure and plasma lipid levels, suggesting a causal relationship between ABO blood groups and the incidence of ACS.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.