26 The effect of exercise or time-control (ie, no exercise) protocols on vascular reactivity was analyzed by means of a repeated-measures ANOVA, followed by the Fisher post hoc test in case Idelalisib in vivo of significant F values. Vascular reactivity was compared between groups using analysis of covariance (ANCOVA) models, where all subjects’ characteristics were considered as covariates. At first, a model was used to compare the baseline vascular reactivity

between groups. Then, a different model was used to compare groups throughout time (ie, ANCOVA main factors: group [wild vs polymorphic] and time [baseline vs 10 minutes vs 60 minutes vs 120 minutes]). In the ANCOVA of the haplotypes, the haplotype containing only wild-type alleles (H1) was separately compared with each of the haplotypes containing polymorphic alleles (ie, H1 vs H2, H1 vs H3, H1 vs H4).26 Greenhouse–Geisser correction was used to correct P values from ANCOVA main effects due to deviation from the sphericity assumption. In case of significant F values, Cohen’s d effect size was calculated. Results are presented as mean ± standard error of the mean. Statistical significance was considered for P ≤ .05 based on 2-tailed comparisons. All analyses were performed using STATISTICA version 8.0 software

(StatSoft Inc, Tulsa, Okla). The characteristics of the entire sample were as follows: age 32 ± 1 years, BMI 25.0 ± 0.3 m/kg, total cholesterol 176 ± 3 mg/dL, HDL 55 ± 1 mg/dL, LDL 104 ± 2 mg/dL, triglycerides 89 ± 3 mg/dL, glycemia 85 ± 1 mg/dL, VO2peak 31.1 ± 0.7 mL/kg/min, HSP inhibitor SBP 114 ± 1 mm Hg, and DBP 73 ± 1 mm Hg. Vascular reactivity increased 10 minutes after exercise in the entire sample (main effect P < 0.01; baseline: 218 ± 11% vs 10 minutes: 284 ± 15%, P = 0.001), remained increased at 60 minutes (239 ± 12%, P = 0.02 vs baseline), and returned to baseline at 120 minutes (210

± 10%, P = 0.83 vs baseline). In the control protocol, there was no change in vascular reactivity (main Gefitinib effect P = 0.96; baseline = 227 ± 24%, 10 minutes = 228 ± 36%, 60 minutes = 237 ± 31%, 120 minutes = 237 ± 29%). The distribution of genotype frequencies for the polymorphisms studied showed no deviation from Hardy–Weinberg’s equilibrium (locus −786, P = 0.93; intron 4, P = 1.00; locus 894, P = 0.70). Two subjects had the 4b4c genotype, and 1 subject had the 4c4c genotype. Because of the low frequency of the c allele, subjects with the 4b4c genotype were grouped with those with the 4b4a genotype, whereas the subject with the 4c4c genotype was grouped with those with the 4a4a genotype. Table I shows partial correlations among eNOS gene polymorphisms and vascular reactivity according to dominant, recessive, and additive models.