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Table 1 S-COMT methylation [% ± SD] with respect to COMT genotype in Blood DNA (twin cohort)

From: Association of COMT genotypes with S-COMT promoter methylation in growth-discordant monozygotic twins and healthy adults

Variant

CG1

CG2b

mean

CG1

CG2b

mean

CG1

CG2b

mean

p-value

rs6269

AA 44.8 ± 3.1

67.1 ± 3.1

56.0 ± 3.0 (n = 10)

AG 40.3 ± 3.0

62.1 ± 3.9

51.2 ± 3.4 (n = 24)

GG 30.6 ± 3.0

51.4 ± 3.0

41.0 ± 2.7 (n = 6)

< 0.01

rs4633

CC 33.2 ± 5.3

54.2 ± 5.8

43.7 ± 5.4 (n = 8)

CT 40.3 ± 3.2

62.0 ± 4.1

51.2 ± 3.5 (n = 22)

TT 44.8 ± 3.1

67.1 ± 3.1

56.0 ± 3.0 (n = 10)

< 0.01

rs4680

AA 44.8 ± 3.1

67.1 ± 3.1

56.0 ± 3.0 (n = 10)

AG 40.3 ± 3.2

62.0 ± 4.1

51.2 ± 3.5 (n = 22)

GG 33.2 ± 5.3

54.2 ± 5.8

43.7 ± 5.4 (n = 8)

< 0.01

  1. Note that similar or equal methylation values across genotype groups for different SNPs result from a high (in the twin cohort almost complete) linkage disequilibrium between rs6269, rs4633, and rs4680. Please note that shown p-values were calculated using one-way ANOVAs, which do not take the interrelatedness of the observations into account.