The concept of exposure when selecting comparison groups for determining individual susceptibility to addiction to cigarette smoking

PLoS One. 2019 Apr 11;14(4):e0214946. doi: 10.1371/journal.pone.0214946. eCollection 2019.

Abstract

Smoking is a leading cause of preventable death. The effect of tobacco is even more contundent in people with mental illness and, in general, cigarette smoking addiction is influenced by genetic factors. The opioid system is involved in the mesolimbic reward system, which is of great importance in addictive behaviors, such as smoking and is influenced by genes such as the OPRM1. The aim of this study was to evaluate if selecting a comparison group that include light smokers versus people that never smoked impacts the results of genetic association studies. In addition, to evaluate the genetic association in different groups of smokers by analyzing independent covariates such as mental illness and clinical dental data. All subjects were participants of the Dental Registry and DNA Repository project. Genotyping was carried out using TaqMan chemistry for two markers in OPRM1 (rs553202 and rs7755635). Logistic regression analyses were performed as implemented in PLINK. The established value for alpha was 5%, and the Hardy-Weinberg equilibrium was evaluated by the chi-square test with one degree of freedom for each marker. 1,897 patients were included, which were allocated to eight distinct groups, according to the frequency and quantity of cigarettes smoked and mental illness status. There was no significant association between the two markers in OPRM1 and smoking. When mental illness and dental clinical data (tooth loss, dental caries, and periodontitis) were used as covariates, there were associations between heavy smoking and OPRM1, when non-smokers were used as comparison. We did not have diet or microbiome data to consider for these dental analyses and suggest that these kinds of data should be always incorporated in the future. Significant results were found only when the covariables mental illness and oral clinical data were added to the analysis.

Publication types

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

MeSH terms

  • Adult
  • Behavior, Addictive* / genetics
  • Behavior, Addictive* / pathology
  • Behavior, Addictive* / physiopathology
  • Cigarette Smoking* / genetics
  • Cigarette Smoking* / pathology
  • Cigarette Smoking* / physiopathology
  • Dental Caries* / genetics
  • Dental Caries* / pathology
  • Dental Caries* / physiopathology
  • Female
  • Humans
  • Male
  • Middle Aged
  • Periodontitis* / genetics
  • Periodontitis* / pathology
  • Periodontitis* / physiopathology
  • Receptors, Opioid, mu / genetics*
  • Tooth Loss* / genetics
  • Tooth Loss* / pathology
  • Tooth Loss* / physiopathology

Substances

  • OPRM1 protein, human
  • Receptors, Opioid, mu

Grants and funding

This work was supported by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brasil (CAPES) - Finance Code 88881.131583/2016-01 (http://www.capes.gov.br) to IWH. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.