Self-reported smoking status, TAS2R38 variants, and propylthiouracil phenotype: an exploratory crowdsourced cohort study.
Chem Senses. 2018 Aug 18;:
Authors: Baker AN, Miranda AM, Garneau NL, Hayes JE
Abstract
TAS2R38 gene variants, which confer sensitivity to specific bitter tastants (e.g., 6-n-propylthiouracil), have been repeatedly associated with lower alcohol use via greater bitterness perception, but research exploring TAS2R38 variation in relation to smoking shows mixed results. In both, the working hypothesis is that 1 or more copies of the functional allele increase bitterness and may provide a barrier to early use. Such a barrier to initiation may, conceivably, manifest as differential rates of current use across diplotypes. Here, an age-diverse convenience sample (n=886) of Denver Museum of Nature & Science guests was used to explore cross-sectional relationships between TAS2R38 diplotype, self-reported tobacco use (current, former, never smoker), and a rapid measure of 6-n-propylthiouracil (PROP) phenotype (bitterness of filter paper discs). TAS2R38 diplotypes were determined by Sanger sequencing. After excluding rare diplotypes, data from 814 participants were analyzed. A mix of current (~10%), former (25%), and never smokers (65%) were included. As expected, there was a relationship between TAS2R38 diplotype and PROP bitterness. However, contrary to our hypothesis, there was no evidence of a relationship between diplotype and smoker status among participants with common TAS2R38 diplotypes. Notably, we observed a relationship between PROP bitterness and smoking status, but the effect was opposite of what was expected: current smokers perceived higher (not lower) bitterness than never smokers. When all the various factors (diplotype, age, sex and smoking status) were included in ANOVA, all remained predictive of PROP bitterness. Reasons for greater phenotypic bitterness among current smokers is unknown and merits further study.
PMID: 30137252 [PubMed - as supplied by publisher]
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