Table 3. The influence of genetic factors on reported maternal adverse effects.
Gene | SNP | Global Minor AlleleFrequency (MAF): | Observed MAF in allstudy participants (N) | Allele | Percent of mothersreporting ADRS (N = 19) | Percent of healthy mothers (N = 218) | P Value | ||||||
ABCB1 | rs1128503 | 0.42 | T = 0.445 (212) | TT | 21 | 25 | 0.21 | ||||||
TC | 37 | 44 | 0.16 | ||||||||||
CC | 42 | 31 | 0.12 | ||||||||||
rs2032582 | 0.34 | A = 0.21 (100) | AA | 21 | 16 | 0.19 | |||||||
T = 0.21 (98) | AT | 5 | 6 | 0.38 | |||||||||
GG | 32 | 39 | 0.16 | ||||||||||
GT | 37 | 35 | 0.19 | ||||||||||
GA | 5 | 3 | 0.38 | ||||||||||
rs1045642 | 0.40 | T = 0.44 (207) | TT | 26 | 21 | 0.19 | |||||||
TC | 32 | 45 | 0.10 | ||||||||||
CC | 42 | 34 | 0.15 | ||||||||||
COMT | rs4680 | 0.39 | A = 0.43 (204) | AA | 21 | 21 | 0.23 | ||||||
AG | 32 | 46 | 0.10 | ||||||||||
GG | 47 | 33 | 0.10 | ||||||||||
rs4633 | 0.39 | T = 0.42 (200) | CC | 47 | 34 | 0.10 | |||||||
CT | 37 | 45 | 0.15 | ||||||||||
TT | 16 | 21 | 0.27 | ||||||||||
rs4818 | 0.32 | C = 0.65 (306) | CC | 37 | 41 | 0.18 | |||||||
CG | 42 | 48 | 0.17 | ||||||||||
GG | 21 | 11 | 0.12 | ||||||||||
OPRM1 | rs1799971 | 0.19 | G = 0.22 (105) | AA | 68 | 62 | 0.18 | ||||||
AG | 32 | 30 | 0.20 | ||||||||||
GG | 0 | 8 | 0.23 | ||||||||||
UGT 2B7 | rs7439366 | 0.47 | T = 0.44 (206) | CC CT TT | 37 37 36 | 36 40 24 | 0.200.190.21 |
Minor allele frequency for polymorphisms in the p-glycoprotein transporter (ABCB1), cathechol-o-methyltransferase (COMT), mu-opioid receptor (OPRM1) and UDP glucuronosyltransferase (UGT) 2B7 in mothers reporting adverse drug reactions (ADR) in themselves compared to those that were asymptomatic (healthy). Significance value was set at P<0.05.