TAS2R38 and its influence on smoking behavior and glucose homeostasis in the German Sorbs

PLoS One. 2013 Dec 2;8(12):e80512. doi: 10.1371/journal.pone.0080512. eCollection 2013.

Abstract

Background: Genetic variants within the bitter taste receptor gene TAS2R38 are associated with sensitivity to bitter taste and are related to eating behavior in the Amish population. Sensitivity to bitter taste is further related to anthropometric traits in an genetically isolated Italian population. We tested whether the TAS2R38 variants (rs713598; rs1726866 and rs10246939) may be related to eating behavior, anthropometric parameters, metabolic traits and consumer goods intake in the German Sorbs.

Materials and methods: The three SNPs were genotyped in a total cohort of 1007 individuals (male/female: 405/602). The German version of the three-factor eating questionnaire was completed by 548 individuals. Genetic association analyses for smoking behavior, alcohol and coffee intake, eating behavior factors (restraint, disinhibition and hunger) and other metabolic traits were analyzed. Further, by combining the three SNPs we applied comparative haplotype analyses categorizing PAV (proline-alanine-valine) carriers (tasters) vs. homozygous AVI (alanin-valine-isoleucine) carriers (non-tasters).

Results: Significant associations of genetic variants within TAS2R38 were identified with percentage of body fat, which were driven by associations in women. In men, we observed significant associations with 30 min plasma glucose, and area under the curve for plasma glucose (0-120 min) (all adjusted P≤0.05). Further, we found that carriers of at least one PAV allele show significantly lower cigarette smoking per day (P = 0.002) as well as, albeit non-significant, lower alcohol intake. We did not confirm previously reported associations between genetic variants of TAS2R38 and eating behavior.

Conclusion: Our data suggest that genetic variation in TAS2R38 is related to individual body composition measures and may further influence consumer goods intake in the Sorbs possibly via individual sensitivity to bitter taste.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Female
  • Germany / ethnology
  • Glucose / metabolism*
  • Humans
  • Male
  • Middle Aged
  • Polymorphism, Single Nucleotide*
  • Receptors, G-Protein-Coupled / genetics*
  • Smoking* / ethnology
  • Smoking* / genetics
  • Smoking* / metabolism
  • Surveys and Questionnaires

Substances

  • Receptors, G-Protein-Coupled
  • taste receptors, type 2
  • Glucose

Grants and funding

This work was supported by grants from the German Diabetes Association (to Y.B., A.T., P.K.) and from the DDS Foundation to (Y.B.). A.T. and Y.B. were supported by the IFB AdiposityDiseases; ADI-K50D and ADI-K7-45 (to Y.B.); K7-37 and K403 (to A.T.). M.K. is funded by ADI-K7-39. IFB AdiposityDiseases is supported by the Federal Ministry of Education and Research (BMBF), Germany, FKZ: 01EO1001. X.L. is financed by a research grant from the DFG (BO/3147-4 to Y.B.). This work was further supported by a Collaborative Research Center granted by the DFG (CRC 1052 “Obesity Mechanisms”): A01 (to. M.S.); B03 (to P.K.) and C01 (to A.T.). K.R is funded by a research grant from the Boehringer Ingelheim Foundation. The publication was supported by a publication allowance from the Graduate Center LIFE Sciences of the Research Academy Leipzig at the University of Leipzig, Germany. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.