Pharmacogenetic influence of eNOS gene variant on endothelial and glucose metabolism responses to L-arginine supplementation: Post hoc analysis of the L-arginine trial

• Published in: Metabolism, clinical and experimental clinical and experimental, 2015-11, Vol.64 (11), p.1582-1591
• Main Authors: Monti, Lucilla D, Galluccio, Elena, Fontana, Barbara, Spadoni, Serena, Comola, Mauro, Marrocco Trischitta, Massimiliano M, Chiesa, Roberto, Comi, Giancarlo, Bosi, Emanuele, Piatti, Piermarco
• Format: Article
• Language: English
• Subjects: Arginine - administration & dosage; Double-Blind Method; Endocrinology & Metabolism; eNOS polymorphism; Glucose - metabolism; Glucose Tolerance Test; Humans; Insulin Secretion; Insulin Sensitivity; L-Arginine; Nitric Oxide Synthase Type III - genetics; Pharmacogenetics; Placebos; Polymorphism, Single Nucleotide
• ISSN: 0026-0495; 1532-8600
• DOI: 10.1016/j.metabol.2015.08.015

Abstract Objective To evaluate whether variants of the eNOS gene are associated with endothelial and metabolic responses to L-arginine (L-arg) supplementation. Material and Methods We examined a single nucleotide polymorphism of the eNOS gene (rs753482-A > C) to investigate the effects of this variant on endothelial function (EF), colony-forming unit–endothelial cell (CFU-EC) number, asymmetric-dimethylarginine (ADMA) level, insulin sensitivity index (ISI), and insulin secretion (IS) in a post hoc analysis of the L-arg trial. The L-arg trial (6.4 g/day for 18 months) was a single-center, randomized, double-blind, parallel-group, placebo-controlled, phase III trial in individuals with impaired glucose tolerance and metabolic syndrome. followed by a 12-month extended follow-up period after termination of the study drug (NCT 00917449). Results At baseline, EF, CFU-EC numbers, ADMA levels, and ISI were impaired in subjects carrying minor allele C (both heterozygotes, AC and homozygotes, CC) as compared to subjects carrying major allele A (homozygotes, AA) (p < 0.01). Compared to placebo, L-arg increased EF, CFU-EC numbers, and ISI, and improved ADMA levels and IS (p < 0.01). The greatest improvements were found in AA subjects treated with L-arg, while the worst results were found in AC + CC subjects treated with placebo. In the placebo-treated subjects, EF, CFU-EC, ISI, and IS were significantly lower and ADMA was significantly higher in AC + CC subjects than in AA subjects. Conclusions Treatment with L-arg induced similar improvements in EF, CFU-EC numbers, ADMA levels, ISI, and IS in both AA subjects and AC + CC subjects. The presence of minor allele resulted in the worst prognosis in terms of EF, CFU-EC numbers, ADMA levels, ISI, and IS during the 30-month observation period.