Skip to main content

Table 3 Risk analysis results of gDMRs methylation levels of imprinted genes and CHD occurrence

From: DNA methylation abnormalities of imprinted genes in congenital heart disease: a pilot study

Imprinted genes

Quantile percentages

Controls

n (%)

CHD

n (%)

Adjusted ORa

(95% CIb)

GRB10

Q1c (< 39.67%)

6(26.1%)

1(4%)

1(reference)

 

Q2–Q3 d (39.67%–44%)

11(47.8%)

3(12%)

1.64(0.14–19.39)

 

Q4e (> 44%)

6(26.1%)

21(84%)

21.00(2.10–210.14)

MEST

Q1 (< 49.36%)

5(22.7%)

1(5%)

1(reference)

 

Q2–Q3 (49.36%–56.07%)

12(54.5%)

9(45%)

3.75(0.371–37.95)

 

Q4 (> 56.07%)

5(22.7%)

10(50%)

10.00(0.907–110.28)

PEG10

Q1 (< 45.2%)

5(22.7%)

14(56%)

16.80(1.60–176.23)

 

Q2–Q3 (45.2%–55.7%)

11(50%)

10(40%)

5.46(0.56–53.52)

 

Q4 (> 55.7%)

6(27.3%)

1(4%)

1(reference)

NAP1L5

Q1 (< 67.14%)

6(26.1%)

9(45%)

3.50(0.64–19.20)

 

Q2–Q3 (67.14%–71.29%)

10(43.5%)

8(40%)

1.87(0.36–9.64)

 

Q4 (> 71.29%)

7(30.4%)

3(15%)

1(reference)

INPP5Ff

Q1 (< 70.39%)

4(23.5%)

17(77.3%)

11.06(2.47–49.53)

 

Q2–Q4 (≥ 70.39%)

13(76.5%)

5(22.7%)

1(reference)

PLAGL1

Q1 (< 40.76%)

6(24%)

11(42.3%)

11.00(1.06–114.09)

 

Q2–Q3 (40.76%–45.82%)

13(52%)

14(53.8%)

6.46(0.68–61.16)

 

Q4 (> 45.82%)

6(24%)

1(3.8%)

1(reference)

MEG3f

Q1 (< 41.83%)

6(25%)

16(80%)

12.00(2.86–50.31)

 

Q2–Q4 (≥ 41.83%)

18(75%)

4(20%)

1(reference)

  1. aOdds ratio
  2. bConfidence interval
  3. c25th percentile
  4. d25th percentile to 75th percentile
  5. e75th percentile. Cut-off value was defined as 25th and 75th percentiles of the control group methylation level. Adjusted for sex by logistic regression
  6. fIndicates that the maximum value of the imprinting gene cases was less than 75% of control group and could not be calculated, so there were divided into two groups