Skip to main content
. 2018 Sep 29;7(19):e03488. doi: 10.1161/JAHA.117.008461

Table 4.

Levels of Quantitative Traits at 1 Year by Genotype and Treatment Arm at Loci With a Nominally Significant Interaction

Gene/Chr/SNP Alleles Placebo+Statin Niacin+Statin
Baseline Year 1 % Change Absolute Change Baseline Year 1 % Change Absolute Change
MAF Minor/Major Trait GT N Mean (SD)a N Mean (SD) Mean (SD) Mean (SD) N Mean (SD) N Mean (SD) Mean (SD) Mean (SD)
MVK 0.47 C/T HDL TT 280 34.9 (5.4) 256 38.1 (7.9) 9.1 (15.9) 3.1 (5.7) 304 34.8 (5.7) 277 45.4 (12.1) 30.8 (25.3) 10.7 (9.3)
 12 TC 474 35.4 (5.5) 435 39.1 (7.4) 10.6 (15.3) 3.6 (5.3) 517 34.5 (5.4) 471 43.5 (10.6) 26.4 (23.1) 9.1 (8.1)
rs10850443 CC 265 34.7 (5.4) 245 38.2 (7.2) 10.5 (16.0) 3.5 (5.3) 211 34.5 (5.8) 189 43.4 (11.2) 26.4 (24.1) 9.0 (8.8)
P Value by GT 0.22 0.26 0.012 0.007
LIPC 0.36 A/G HDL GG 404 34.6 (5.7) 376 38.2 (7.5) 11.7 (15.9) 3.9 (5.3) 429 34.5 (5.8) 387 43.2 (11.5) 25.8 (23.3) 8.9 (8.6)
15 GA 465 35.1 (5.3) 428 38.4 (7.1) 9.4 (15.3) 3.2 (5.3) 472 34.5 (5.5) 430 44.5 (11.2) 29.0 (24.7) 10.0 (8.6)
rs1532085 AA 151 36.1 (5.3) 133 39.6 (8.2) 8.1 (15.4) 3.0 (6.0) 132 35.1 (5.3) 121 44.9 (9.7) 29.2 (23.6) 10.0 (8.2)
P Value by GT 0.006 0.026 0.037 0.031
PABPC4 0.23 G/A HDL AA 617 35.1 (5.4) 567 38.8 (7.3) 11.0 (5.6) 3.7 (5.4) 580 34.9 (5.8) 530 44.4 (11.2) 27.2 (23.5) 9.4 (8.6)
1 AG 361 35.3 (5.5) 332 38.3 (7.7) 9.1 (15.6) 3.1 (5.5) 390 34.3 (5.4) 354 43.8 (11.3) 28.4 (24.6) 9.7 (8.8)
rs4660293 GG 42 32.9 (5.8) 38 34.7 (6.3) 7.3 (16.4) 2.1 (5.6) 64 34.0 (5.5) 55 43.8 (10.2) 28.7 (25.0) 9.7 (8.5)
P Value by GT 0.029 0.031 0.33 0.41
AMPD3 0.18 G/A HDL AA 664 35.1 (5.4) 617 38.4 (7.6) 9.8 (15.9) 3.3 (5.5) 698 34.6 (5.7) 633 44.2 (11.3) 28.2 (23.5) 9.7 (8.6)
11 AG 323 35.1 (5.7) 292 38.8 (7.3) 10.9 (15.2) 3.7 (5.3) 300 34.6 (5.5) 275 43.9 (11.1) 27.7 (25.5) 9.5 (8.7)
rs2923084 GG 33 33.4 (5.1) 28 36.8 (6.7) 9.9 (15.9) 3.2 (5.0) 36 34.9 (5.3) 31 41.2 (9.2) 18.2 (18.5) 6.3 (6.9)
P Value by GT 0.28 0.30 0.26 0.2
SPTLC3 0.39 A/G LDL GG 376 76.1 (22.8) 342 71.3 (19.1) −2.7 (28.6) −5.6 (24.1) 406 74.2 (21.8) 361 68.9 (20.7) −1.1 (37.4) −5.4 (25.5)
20 GA 482 72.3 (21.0) 448 70.6 (18.5) 1.2 (33.1) −3.3 (23.9) 479 73.1 (22.5) 443 65.6 (19.8) −4.5 (38.1) −8.5 (26.3)
rs364585 AA 162 72.4 (22.4) 144 69.2 (7.3) 1.2 (34.0) −3.6 (24.5) 149 73.2 (22.5) 134 65.1 (15.1) −5.2 (37.3) −9.0 (23.8)
P Value by GT 0.08 0.22 0.11 0.043
TOM1 0.34 A/G TC GG 456 144.4 (24.6) 413 143.9 (24.6) 1.5 (19.6) −0.7 (29.5) 462 146.2 (27.6) 422 138.8 (27.5) −3.5 (21.2) −8.3 (32.0)
22 GA 441 145.4 (26.4) 408 143.7 (24.4) 0.8 (19.3) −1.9 (28.5) 437 142 (25.7) 392 136.5 (26.2) −1.5 (22.2) −5.2 (31.4)
rs138777 AA 123 149.9 (30.2) 117 144.2 (8.4) −0.08 (25.7) −5.5 (38.1) 135 147.3 (36.2) 128 141 (26.4) −2.2 (21.3) −6.5 (33.9)
P Value by GT 0.35 0.38 0.14 0.12
PDXDC1 0.39 T/C TG CC 392 156 (128, 212) 365 156 (119, 207) −4 (−23, 21) −7 (−36, 32) 359 178 (140, 235) 331 117 (85, 160) −32.0 (−49, −13) −54 (−97, −21)
16 CT 471 165 (134, 216) 431 158 (123, 206) −3 (−26, 24) −5 (−43, 35) 516 162 (130, 213) 466 120 (83, 171) −29.4 (−48, −1.5) −46 (−80, −2)
rs3198697 TT 157 173 (136, 222) 142 154 (113, 207) −9 (−29, 11) −16 (−47, 20) 159 156 (127, 203) 145 124 (85, 167) −24.5 (−46, −3) −38 (−77, −5)
P Value by GT 0.13 0.077 0.034 0.015
CYP26A1 0.44 A/G TG GG 331 165 (135, 224) 306 161 (121, 213) −4 (27, 20) −7 (−44, 30) 311 165 (129, 225) 288 131 (90, 187) −23 (−42, 2) −36 (−76, 3)
10 GA 493 159 (131, 203) 451 155 (118, 206) −4 (−23, 22) −7 (−44, 33) 525 171 (135, 217) 473 114 (82, 161) −32 (−51, −11) −54 (−92, −18)
rs2068888 AA 196 161 (133, 222) 181 157 (123, 204) −7 (−27, 21) −11 (−45, 32) 198 161 (126, 210) 181 115 (83, 157) −32 (−48, −10) −48 (−85, −16)
P Value by GT 0.40 0.59 <0.0001 0.001

Chr indicates chromosome; GT, genotype; HDL, high‐density lipoprotein cholesterol; IQR, interquartile range; LDL, low‐density lipoprotein cholesterol; MAF, minor allele frequency; SNP, single nucleotide polymorphism; TC, total cholesterol; TG, triglycerides.

a

TG reported as median (IQR).