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. 2012 Oct;53(10):2205–2213. doi: 10.1194/jlr.P025080

TABLE 4.

Postprandial changes in LDI and circulating measures of vascular function before (time 0) and 240 min following an oral fat load of either SFA or SFA + LC n-3 PUFA

Females (mean ± SEM)
Males (mean ± SEM)
Differences between the Two Fat Loads
Asp289 (n = 14) Glu298 (n = 15) Asp289 (n = 15) Glu298 (n = 15) P (genotype all) P (gender all)
LDI AUC
 LDI-Ach (AU) SFA fat load 596 ± 445 589 ± 347 524 ± 444 476 ± 460
 LDI-Ach (AU)SFA + LC n-3 PUFA fat load 1296 ± 314* 309 ± 339 878 ± 437 569 ± 520 0.408 0.951
 LDI-SNP (AU) SFA fat load 393 ± 424 626 ± 396 271 ± 578 926 ± 469
 LDI-SNP (AU) SFA + LC n-3 PUFA fat load 1453 ± 347 719 ± 190 557 ± 659 393 ± 362 0.118 0.180
Circulating measures
 ET-1 (ng/ml) SFA fat load 0.01 ± 0.01 −0.03 ± 0.05 −0.10 ± 0.09 0.04 ± 0.10
 ET-1 (ng/ml) SFA +LC n3 PUFA fat load −0.02 ± 0.08 0.01 ± 0.06 0.06 ± 0.05 0.02 ± 0.08 0.591 0.590
 NOx (μM) SFA fat load −4.73 ± 1.18 −3.01 ± 0.84 −2.29 ± 1.0 −4.59 ± 0.98
 NOx (μM) SFA +LC n3 PUFA fat load −2.89 ± 1.14 −3.86 ± 1.58 −2.35 ± 0.81 −2.37 ± 0.99 0.88 0.61

Statistical significance of difference between genotypes within a gender: *P ≤ 0.05.