Ontology highlight
ABSTRACT: Background
Aspirin use is an effective strategy for the chemoprevention of colorectal cancer, even at low doses. However, in order to implement aspirin interventions, risk-benefit balances and biologic mechanisms need to be better defined; to further this aim, we used a metabolomics approach.Methods
We metabolically profiled 40 healthy, nonsmoking men and women ages 20 to 45 years enrolled in a randomized, double-blind, crossover trial of 325 mg aspirin/day over a period of 60 days. Gas and liquid chromatography-mass spectrometry were used to comprehensively profile participants' plasma samples after aspirin and placebo interventions.Results
A total of 363 metabolites, covering most human biochemical pathways, were measured. Compared with placebo-treated participant
SUBMITTER: Liesenfeld DB
PROVIDER: S-EPMC4911817 | biostudies-literature | 2016 Jan
REPOSITORIES: biostudies-literature