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. 2014 Sep 16;5:210. doi: 10.3389/fphar.2014.00210

Table 3B.

Genotype-by-treatment interaction results for genetic model (additive and dominant) among African Americans.

Out-come AGT variant Number of cases (col %) ORs and p-values for genetic model, African Americans
CHL AML LIS CHL vs. AML CHL vs. LIS LIS vs. AML
CHD (n = 753) rs7079 CC 259 (78.3%) 175 (87.1%) 175 (85.0%) p = 0.01; OR = 1.9; CI(1.1–3.0) p = 0.06; OR = 1.6; CI (1.0–2.5) p = 0.54; OR = 1.2; CI(0.7–2.1)
AC&AA 72 (21.7%) 26 (12.9%) 31 (15%)
rs5051 TT 237 (71.6%) 150 (73.2%) 162 (78.3%) p = 0.69; OR = 1.1; CI(0.7–1.6) p = 0.09; OR = 1.4; CI(1.0–2.1) p = 0.23; OR = 0.8; CI(0.5–1.2)
TC&CC 94 (28.4%) 55 (26.8%) 45 (21.7%)
rs3789678 CC 215 (64.6%) 139 (69.9%) 126 (60.9%) p = 0.21; OR = 1.3; CI(0.9–1.9) p = 0.39; OR = 0.9; CI(0.6–1.2) p = 0.06; OR = 1.5; CI(1.0–2.2)
TC&TT 118 (35.4%) 60 (30.1%) 81 (39.1%)
rs2493133 CC 211 (64.5%) 134 (68.7%) 145 (71.1%) p = 0.33; OR = 1.2; CI(0.8–1.8) p = 0.12; OR = 1.4; CI(0.9–2.0) p = 0.61; OR = 0.9; CI(0.6–1.4)
TC&TT 116 (35.5%) 61 (31.3%) 59 (28.9%)
rs2493129 GG 288 (86.0%) 164 (82.4%) 180 (86.5%) p = 0.27; OR = 0.8; CI(0.5–1.2) p = 0.85; OR = 1.0; CI(0.6–1.7) p = 0.25; OR = 0.7; CI(0.4–1.3)
AG&AA 47 (14%) 35 (17.6%) 28 (13.5%)
rs2478544 GG 96 (31.3%) 48 (25.7%) 63 (32.1%) p = 0.31; OR = 0.9; CI(0.7–1.1) p = 0.97; OR = 1.0; CI(0.8–1.3) p = 0.34; OR = 0.9; CI(0.7–1.2)
GC 144 (47.0%) 96 (51.3%) 89 (45.4%)
CC 67 (21.8%) 43 (23.0%) 44 (22.5%)
rs11122576 AA 294 (87.5%) 191 (94.6%) 181 (87.0%) p = 0.006; OR = 2.5; CI(1.2–4.9) p = 0.87; OR = 1.0; CI(0.6–1.6) p = 0.01; OR = 2.6; CI(1.2–5.4)
AG&GG 42 (12.5%) 11 (5.5%) 27 (13%)
HF (n = 634) rs7079 CC 190 (80.9%) 181 (86.2%) 154 (86.0%) p = 0.13; OR = 1.5; CI(0.9–2.5) p = 0.16; OR = 1.5; CI(0.9–2.5) p = 0.96; OR = 1.0; CI(0.6–1.8)
AC&AA 45 (19.1%) 29 (13.9%) 25 (14%)
rs5051 TT 157 (67.1%) 160 (76.2%) 125 (69.8%) p = 0.03; OR = 1.6; CI(1.0–2.4) p = 0.55; OR = 1.1; CI(0.7–1.7) p = 0.16; OR = 1.4; CI(0.9–2.2)
TC&CC 77 (32.9%) 50 (23.8%) 54 (30.2%)
rs3789678 CC 147 (62.8%) 124 (60.5%) 100 (55.9%) p = 0.59; OR = 0.9; CI(0.7–1.3) p = 0.16; OR = 0.8; CI(0.6–1.1) p = 0.38; OR = 1.2; CI(0.8–1.6)
TC 76 (32.5%) 70 (34.2%) 68 (38.0%)
TT 11 (4.7%) 11 (5.4%) 11 (6.2%)
rs2493133 CC 145 (62.5%) 142 (69.3%) 117 (66.5%) p = 0.14; OR = 1.4; CI(0.9–2.0) p = 0.41; OR = 1.2; CI(0.8–1.8) p = 0.56; OR = 1.1; CI(0.7–1.8)
TC&TT 87 (37.5%) 63 (30.7%) 59 (33.5%)
rs2493129 GG 207 (87.7%) 189 (89.2%) 143 (80.3%) p = 0.64; OR = 1.2; CI(0.6–2.1) p = 0.04; OR = 0.6; CI(0.3–1.0) p = 0.02; OR = 2.0; CI(1.1–3.6)
AG&AA 29 (12.3%) 23 (10.9%) 35 (19.7%)
rs2478544 GG 72 (32.6%) 56 (28.4%) 63 (38.7%) p = 0.56; OR = 0.9; CI(0.7–1.2) p = 0.35; OR = 1.1; CI(0.9–1.5) p = 0.14; OR = 0.8; CI(0.6–1.1)
GC 105 (47.5%) 102 (51.8%) 69 (42.3%)
CC 44 (20.0%) 39 (19.8%) 31 (19.0%)
rs11122576 AA 214 (91.1%) 196 (92.9%) 161 (89.0%) p = 0.48; OR = 1.3; CI(0.6–2.6) p = 0.47; OR = 0.8; CI(0.4–1.5) p = 0.18; OR = 1.6; CI(0.8–3.3)
AG&GG 21 (8.9%) 15 (7.2%) 20 (11%)

CHL, chlorthalidone; AML, amlodipine; LIS, lisinopril; CHD, coronary heart disease; HF, heart failure.

Dominant model was used for SNP which has any cell size less than 10 observations by collapsing minor allele homozygotes with heterozygotes which was compared to common allele homozygotes. Additive model coded common homozygotes as 0, heterozygotes as 1; rare homozygotes as 2; and assumed linearity (1-degree of freedom test).