Research Article

The NLRP3 Genetic Variant (rs10754555) Reduces the Risk of Adverse Outcome in Middle-Aged Patients with Chronic Coronary Syndrome

Table 2

Frequency of the NLRP3 variant in the total population and according to type of new clinical events and sex.

CCCGGGG-allele frequency value

Total cohort4144481340.360
With clinical event+4944130.3310.303
-3654041210.363
UAP+19950.2890.058
-3954391290.362
AMI+191430.2780.164
-3954341310.362
Stroke+81730.4110.157
-4064311310.358
Death+3420.4440.615
-4114441320.359
Men3263441080.3600.684
Women88104260.358

Number of available DNA . UAP: unstable angina pectoris; AMI: acute myocardial infarction. values represent the difference in G-allele frequency (CG and GG combined) according to subgroups (chi-square test).