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Table 2 Multivariable-adjusted hazard ratios for CHD by MEOX2 SNPs

From: Coronary risk in relation to genetic variation in MEOX2 and TCF15 in a Flemish population

SNP Event

N° events/at risk

Hazard ratio

P

P BH

Minor allele carriers

Major allele homozygotes

rs10777

GG + TG

TT

   

 All coronary events

59/911

47/1116

1.56 (1.06–2.29)

0.024

0.029

 Myocardial infarction

31

22

1.75 (1.01–3.03)

0.045

0.054

 Coronary revascularisation

42

36

1.42 (0.90–2.24)

0.13

0.14

 Ischaemic cardiomyopathy

16

6

4.68 (1.86–11.77)

0.0011

0.0066

rs12056299

TT + CT

CC

   

 All coronary events

51/764

55/1263

1.68 (1.17–2.41)

0.0052

0.016

 Myocardial infarction

28

25

2.05 (1.20–3.51)

0.0087

0.042

 Coronary revascularisation

37

41

1.59 (1.02–2.49)

0.041

0.082

 Ischaemic cardiomyopathy

14

8

3.37 (1.49–7.62)

0.0036

0.011

rs7787043

CC + TC

TT

   

 All coronary events

74/1111

32/916

1.72 (1.13–2.62)

0.011

0.023

 Myocardial infarction

38

15

1.82 (1.02–3.27)

0.044

0.054

 Coronary revascularisation

54

24

1.68 (1.02–2.77)

0.041

0.082

 Ischaemic cardiomyopathy

16

6

2.22 (0.84–5.86)

0.11

0.20

rs4532497

CC + TC

TT

   

 All coronary events

66/1004

40/1023

1.80 (1.22–2.66)

0.0031

0.016

 Myocardial infarction

33

20

1.88 (1.03–3.42)

0.040

0.054

 Coronary revascularisation

50

28

1.88 (1.20–2.96)

0.0062

0.037

 Ischaemic cardiomyopathy

14

8

1.97 (0.80–4.83)

0.14

0.20

rs6959056

AA + GA

GG

   

 All coronary events

59/1382

47/645

0.62 (0.42–0.92)

0.017

0.025

 Myocardial infarction

27

26

0.52 (0.31–0.88)

0.014

0.042

 Coronary revascularisation

46

32

0.71 (0.45–1.12)

0.14

0.14

 Ischaemic cardiomyopathy

12

10

0.75 (0.33–1.70)

0.49

0.49

rs1050290

CC + TC

TT

   

 All coronary events

73/1194

33/833

1.50 (1.00–2.26)

0.049

0.049

 Myocardial infarction

36

17

1.48 (0.81–2.70)

0.20

0.20

 Coronary revascularisation

55

23

1.59 (0.99–2.56)

0.055

0.083

 Ischaemic cardiomyopathy

16

6

1.97 (0.75–5.16)

0.17

0.20

  1. Numbers of events do not add up, because only the first event in each category was analysed. Hazard ratios (95 % confidence interval) express the risk of minor allele carriers vs. major allele homozygotes, account for family clusters, and were adjusted for baseline characteristics including sex, age, body mass index, systolic pressure, total-to-HDL cholesterol ratio, smoking and drinking, and antihypertensive drug treatment. P and P BH indicate the significance of the hazard ratios without and with Benjamini-Hochberg’s correction for multiple testing