J Med Genet

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH REGISTER
[Advanced]

The most recent version of this article was published on 1 September 2008

J Med Genet. Published Online First: 4 June 2008. doi:10.1136/jmg.2008.057844
Copyright © 2008 by the BMJ Publishing Group Ltd.

This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
jmg.2008.057844v1
45/9/578    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this link to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Google Scholar
Right arrow Articles by Mangold, J. E
Right arrow Articles by Li, M. D
PubMed
Right arrow PubMed Citation
Right arrow Articles by Mangold, J. E
Right arrow Articles by Li, M. D
Right arrowPubmed/NCBI databases
*Gene*GEO Profiles
*HomoloGene*Nucleotide
*OMIM*Protein
*UniGene

Original articles

Bitter taste receptor gene polymorphisms are an important factor in the development of nicotine dependence in African Americans

Jamie E Mangold 1, Thomas J Payne 2, Jennie Z Ma 1, Guobo Chen 1 and Ming D Li 1*

1 U of VA, United States
2 U of Mississippi Medical Ctr, United States

* To whom correspondence should be addressed. E-mail: ml2km{at}virginia.edu.

Accepted 23 April 2008


*   Abstract

Context: Bitter sensitivity varies among individuals and ethnic groups partly due to polymorphisms in taste receptor genes (TAS2Rs). Although previous psychophysical studies suggest that taste status plays a role in nicotine dependence (ND), genetic evidence is lacking.

Objectives: To determine whether single nucleotide polymorphisms (SNPs) in TAS2R16 and TAS2R38 are associated with ND and if the effects differ by sex and ethnicity. Design, Setting, and Participants: 2037 individuals from 602 nuclear families of African American (AA) or European American (EA) origin were recruited from the Mid-South States during 1999-2004.

Main Outcome Measure(s): ND was assessed by three measures: indexed Smoking Quantity (SQ), Heaviness of Smoking Index (HSI), and the Fagerström Test for Nicotine Dependence (FTND). Peripheral blood samples were obtained for DNA extraction and genotyping.

Results: The TAS2R38 taster haplotype PAV was inversely associated (P = 0.0165), and the nontaster haplotype AVI was positively associated (P = 0.0120), with SQ in AA smokers. The nontaster haplotype was positively associated with all ND measures in AA female smokers (P = 0.01~0.003). No significant associations were observed in the EA sample. Conclusions: TAS2R38 polymorphisms are an important factor in determining ND in AAs. Heightened oral sensitivity confers protection against ND. Conversely, decreased sensitivity represents a risk factor for ND, especially in AA females. Together, our findings suggest that taster status plays a role in governing the development of ND and may represent a way to identify individuals at risk for developing ND, particularly in AA smokers.








HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH REGISTER
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2008 by the BMJ Publishing Group Ltd.