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Table 4 Association of F5:c.6665A > G, MTHFR: c.665C > T and c.1286A > C genotypes with onset and severity of preeclampsia

From: MTHFR and F5 genetic variations have association with preeclampsia in Pakistani patients: a case control study

SNV

Genotype

Onset of preeclampsia

Severity of preeclampsia

Early (N = 50)

Late (N = 75)

OR (95% CI)

p-value

P*

Mild (N = 55)

Severe (N = 70)

OR (95% CI)

p-value

P*

F5:c.6665A > G

AA

43 (34.4%)

66 (52.8%)

1.00

–

–

50 (40%)

59 (47.2%)

1.00

–

–

AG

6 (4.8%)

8 (6.4%)

1.27 (0.41–3.40)

0.68

1.02

4 (3.2%)

10 (8%)

0.46 (0.13–1.56)

0.21

0.84

GG

1 (0.8%)

1 (0.8%)

1.51 (0.09–25.51)

0.77

1.026

1 (0.8%)

1 (0.8%)

1.12 (0.07–18.81)

0.94

0.94

MTHFR:c.665C > T

CC

40 (32%)

62 (49.6%)

1.00

–

–

46 (36.8%)

56 (44.8%)

1.00

–

–

CT

8 (6.4%)

12 (9.6%)

1.08 (0.40–2.88)

0.89

1.068

7 (5.6%)

13 (10.4%)

0.65 (0.24–1.77)

0.40

0.96

TT

2 (1.6%)

1 (0.8%)

2.88 (0.25–33.20)

0.40

0.8

2 (1.6%)

1 (0.8%)

2.20 (0.19–25.5)

0.53

0.908

MTHFR:c.1286A > C

AA

32 (25.6%)

29 (23.2%)

1.00

–

–

27 (21.6%)

34 (27.2%)

1.00

–

–

AC

8 (6.4%)

38 (30.4%)

0.19 (0.08–0.49)

< 0.001

0.012

15 (12%)

31 (24.8%)

0.65 (0.28–1.5)

0.31

0.92

CC

10 (8%)

8 (6.4%)

1.08 (0.37–3.19)

0.89

0.97

13 (10.4%)

5 (4%)

3.26 (1.03–10.30)

0.04

0.24

  1. P*: Benjamini-Hochberg adjusted P value. Bold fonts indicate significant P-value