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Table 3 Analysis of FCN2 polymorphisms in SSc cases and controls

From: Potential role of the lectin pathway of complement in the pathogenesis and disease manifestations of systemic sclerosis: a case-control and cohort study

Variables

Cases

Controls

Univariate matched analysis

(n = 90)

(n = 90)

OR (95% CI)

Pvalue

FCN2 promoter variants, n (%)

    

 FCN2 -986, n (%)

    

  G/G

27 (30)

22 (24)

Reference

 

  G/A

39 (43)

44 (49)

0.7 (0.3-1.5)

0.4

  A/A

24 (27)

24 (27)

0.8 (0.4-1.7)

0.6

 FCN2 - 602, n (%)

    

  G/G

57 (63)

63 (70)

Reference

 

  G/A

25 (28)

23 (26)

1.1 (0.6-2.3)

0.7

  A/A

8 (9)

4 (4)

2.0 (0.6-6.7)

0.25

 FCN2 - 557, n (%)

    

  A/A

65 (72)

76 (84)

Reference

 

  A/G

23 (26)

13 (14)

2.1 (1.0-4.7)

0.07

  G/G

2 (2)

1 (1)

2 (0.2-22.0)

0.6

 FCN2 - 4, n (%)

    

  A/A

53 (59)

41 (46)

Reference

 

  A/G

35 (39)

41 (46)

0.7 (0.4-1.2)

0.18

  G/G

2 (2)

8 (9)

0.2 (0.04-0.99)

0.048

FCN2 exon variants, n (%)

    

 FCN2 + 6359, n (%)

    

  C/C

49 (54)

40 (44)

Reference

 

  C/T

39 (44)

40 (44)

0.8 (0.4-1.4)

0.4

  T/T

2 (2)

10 (11)

0.2 (0.04-0.8)

0.03

 FCN2 + 6424, n (%)

    

  G/G

65 (72)

74 (82)

Reference

 

  G/T

22 (24)

15 (17)

1.6 (0.8-3.2)

0.2

  T/T

3 (3)

1 (1)

3.4 (0.4-33.0)

0.3

FCN2 haplotypes, n (%)

    

  GGAACG

31 (35)

37 (41)

Reference

 

  AGAGTG

18 (20)

26 (30)

0.6 (0.4-1.1)

0.1

  AAAACG

19 (22)

14 (15)

1.4 (0.8-2.4)

0.3

  GGGACT

11 (13)

7 (7)

1.7 (0.7-3.8)

0.2

  AGAACG

4 (4)

2 (2)

1.7 (0.5-5.0)

0.4

  1. CI, confidence interval; FCN2, ficolin-2; OR, odds ratio; SD, standard deviation; SSc, systemic sclerosis.