Abstract Objective: To investigate whether taste perception of two artificial sweeteners—aspartame and neohesperidin dihydrochalcone (NHDC)—is causally associated with the risk of site-specific cancers. Design: A two-sample Mendelian randomization (MR) study. Setting: Genetic instruments for taste perception (6 for aspartame; 13 for NHDC) were obtained from a genome-wide association study (GWAS) of Australian adolescents, and cancer outcome data were sourced from publicly available GWAS datasets. Participants: Genetic data for taste perception from 1,757 Australian adolescents and genetic data for cancers from large-scale GWAS cohorts, including UK Biobank (n=500,000) and FinnGen (n=500,000). Results: A one standard deviation increase in the genetically predicted perceived intensity of NHDC was associated with an increased risk of male genital cancer (OR = 1.11, 95% CI: 1.04–1.19) and prostate cancer (OR = 1.03, 95% CI: 1.01–1.08) based on FinnGen data. These associations persisted after multivariable MR adjustment for glucose and aspartame perception but were not replicated in the UK Biobank. A weak protective association between aspartame perception and cervical cancer (OR = 0.998, 95% CI: 0.997–0.999) was observed, but this attenuated to null in sensitivity analyses. Conclusions: This study found no compelling evidence that perception of aspartame or NHDC during adolescence causally influences later-life cancer risk. The findings highlight the importance of evaluating individual artificial sweeteners separately in future research examining potential health effects.
Crick et al. (Mon,) studied this question.