Filip Ottosson

Background Metabolite profiles provide snapshots of the overall effect of numerous exposures accumulated over life courses, which may lead to health outcomes in the future. Objective We hypothesized that the risk of all‐cause mortality is linked to alterations in metabolism earlier in life, which are reflected in plasma metabolite profiles. We aimed to identify plasma metabolites associated with future risk of all‐cause mortality. Methods Through metabolomics, 110 metabolites were measured in 3833 individuals from the Malmö Diet and Cancer—Cardiovascular Cohort (MDC‐CC). A total of 1574 deaths occurred within an average follow‐up time of 22.2 years. Metabolites that were significantly associated with all‐cause mortality in MDC‐CC were replicated in 1500 individuals from Malmö Preventive Project re‐examination (MPP), among whom 715 deaths occurred within an average follow‐up time of 11.3 years. Results Twenty two metabolites were significantly associated with all‐cause mortality in MDC‐CC, of which 13 were replicated in MPP. Levels of trigonelline, glutamate, dimethylglycine, C18‐1‐carnitine, C16‐1‐carnitine, C14‐1‐carnitine, and 1‐methyladenosine were associated with an increased risk, while levels of valine, tryptophan, lysine, leucine, histidine, and 2‐aminoisobutyrate were associated with a decreased risk of all‐cause mortality. Conclusion We used metabolomics in two Swedish prospective cohorts and identified replicable associations between 13 metabolites and future risk of all‐cause mortality. Novel associations between five metabolites—C18‐1‐carnitine, C16‐1‐carnitine, C14‐1‐carnitine, trigonelline, and 2‐aminoisobutyrate—and all‐cause mortality were discovered. These findings suggest potential new biomarkers for the prediction of mortality and provide insights for understanding the biochemical pathways that lead to mortality.