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. Author manuscript; available in PMC: 2009 Jan 19.
Published in final edited form as: Circulation. 2008 Jan 7;117(4):517–525. doi: 10.1161/CIRCULATIONAHA.107.706317

Table 2.

Dose-Dependent Tyramine Response: Prediction by SNPs in Presynaptic Pathway

Repeated-Measures ANOVA
Gene Function/Locus Name Domain Position* F Statistic P
Catecholamine biosynthesis
TH Promoter C-824T 0.59 0.88
DBH Promoter C-1021T 0.31 0.99
CYB561 Intron 1 C719G 2.80 <0.001
Catecholamine storage
CHGA 3′-UTR C11825T 1.62 0.06
CHGA Exon 6 Glu246Asp 0.88 0.60
CHGA Promoter G-462A 1.28 0.21
CHGB 3′-UTR C13612A 1.45 0.12
CHGB Exon 4 Glu348Glu 2.44 0.002
Catecholamine transport
VMAT1=SLC18A1 3′-UTR T38292C 1.30 0.20
VMAT2=SLC18A2 Intron 12 C25851T 1.32 0.23
NET1=SLC6A2 Exon 9 Thr429Thr 1.25 0.23
Storage vesicle acidification
ATP6V1A Intron 1 A31599G 1.00 0.46
ATP6V1B1 Exon 1 Ile30thr 1.74 0.038
Catecholamine metabolism
 and degradation
MAOA Exon 8 Arg297Arg 3.32 (1.26) <0.001 (0.27)
MAOB Intron 13 A113683G 0.75 (0.81) 0.73 (0.60)
FMO3 Exon 4 Glu158Lys 1.33 0.18
COMT Exon 4 Met158Val 0.56 0.91

All analyses performed with ethnicity as a covariate. Sexes were evaluated separately for SNPs on the X chromosome (MAOA, MAOB).

*

For position notations, see legend for Table 1.

From female subjects only

from male subjects only.

Data in parentheses are for male subjects only. Degrees of freedom for repeated-measures ANOVA: df=8 within subjects, df=2 between subjects, and df=16 for genotype-by-dose interaction.