Author:
Ghosh Nilanjana,Lejonberg Carl,Czuba Tomasz,Dekkers Koen,Robinson Richard,Ärnlöv Johan,Melander Olle,Smith Maya Landenhed,Evans Anne M.,Gidlöf Olof,Gerszten Robert E.,Lind Lars,Engström Gunnar,Fall Tove,Smith J. Gustav
Abstract
AbstractPlasma metabolomics holds potential for precision medicine, but limited information is available to compare the performance of such methods across multiple cohorts. We compared plasma metabolite profiles after an overnight fast in 11,309 participants of five population-based Swedish cohorts (50–80 years, 52% women). Metabolite profiles were uniformly generated at a core laboratory (Metabolon Inc.) with untargeted liquid chromatography mass spectrometry and a comprehensive reference library. Analysis of a second sample obtained one year later was conducted in a subset. Of 1629 detected metabolites, 1074 (66%) were detected in all cohorts while only 10% were unique to one cohort, most of which were xenobiotics or uncharacterized. The major classes were lipids (28%), xenobiotics (22%), amino acids (14%), and uncharacterized (19%). The most abundant plasma metabolome components were the major dietary fatty acids and amino acids, glucose, lactate and creatinine. Most metabolites displayed a log-normal distribution. Temporal variability was generally similar to clinical chemistry analytes but more pronounced for xenobiotics. Extensive metabolite-metabolite correlations were observed but mainly restricted to within each class. Metabolites were broadly associated with clinical factors, particularly body mass index, sex and renal function. Collectively, our findings inform the conduct and interpretation of metabolite association and precision medicine studies.
Funder
Hjärt-Lungfonden
Vetenskapsrådet
European Research Council
Knut och Alice Wallenbergs Stiftelse
Göteborgs Universitet
Skånes universitetssjukhus
Swedish National Health Service
University of Gothenburg
Publisher
Springer Science and Business Media LLC