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. 2022 Jul 22;13:937639. doi: 10.3389/fgene.2022.937639

TABLE 3.

Association of the MTHFR (rs1801133) polymorphism with risk of developing HTN.

SNP Hypertensive (n; %) Non-hypertensive (n; %) Crude odds ratios (95%CI) p-Value Adjusted odds ratios (95%CI) p-Value
rs1801133 (HWE, p = 0.069)
Genotypic
 CC (254; 91) (144; 89) 1.0* 1.0*
 CT (21; 8) (18; 11) 0.64 (0.33–1.25) 0.19 0.75 (0.29–1.95) a 0.56
 TT (3; 1) (0; 0) - - - -
Dominant
 CC (254; 91) (144; 89) 1.0* 1.0*
 CT + TT (24; 9) (18; 11) 0.75 (0.40–1.43) 0.34 0.86 (0.35–2.16) a 0.75
Recessive
 CC + CT (275; 99) (162; 100) 1.0* 1.0*
 TT (3; 1) (0; 0) - - - -
Co-dominant
 CC + TT (18; 8) (22; 11) 1.0* 1.0*
 CT (144; 92) (256; 89) 1.48 (0.72–2.84) 0.24 1.33 (0.51–3.48) a 0.55
Allelic
 C (529; 95) (306; 95) 1.0*
 T (27; 5) (18; 5) 0.86 (0.47–1.60) 0.65
a

adjusted for age, gender, smoking status, BMI and blood glucose levels.

*p-Value > 0.05 was considered statistically not significant.

HWE, Hardy-Weinberg Equilibrium; MTHFR, methylenetetrahydrofolate reductase; BMI, body mass index; CI, confidence interval.