The Reversion of cg05575921 Methylation in Smoking Cessation: A Potential Tool for Incentivizing Healthy Aging

Genes (Basel). 2020 Nov 27;11(12):1415. doi: 10.3390/genes11121415.

Abstract

Smoking is the largest preventable cause of mortality and the largest environmental driver of epigenetic aging. Contingency management-based strategies can be used to treat smoking but require objective methods of verifying quitting status. Prior studies have suggested that cg05575921 methylation reverts as a function of smoking cessation, but that it can be used to verify the success of smoking cessation has not been unequivocally demonstrated. To test whether methylation can be used to verify cessation, we determined monthly cg05575921 levels in a group of 67 self-reported smokers undergoing biochemically monitored contingency management-based smoking cessation therapy, as part of a lung imaging protocol. A total of 20 subjects in this protocol completed three months of cotinine verified smoking cessation. In these 20 quitters, the reversion of cg05575921 methylation was dependent on their initial smoking intensity, with methylation levels in the heaviest smokers reverting to an average of 0.12% per day over the 3-month treatment period. In addition, we found suggestive evidence that some individuals may have embellished their smoking history to gain entry to the study. Given the prominent effect of smoking on longevity, we conclude that DNA methylation may be a useful tool for guiding and incentivizing contingency management-based approaches for smoking cessation.

Keywords: AHRR; DNA methylation; cg05575921; contingency management; smoking cessation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adult
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / physiology*
  • Biomarkers
  • Cigarette Smoking / blood
  • Cigarette Smoking / genetics*
  • Clinical Trials as Topic
  • Cotinine / blood
  • CpG Islands / genetics*
  • DNA Methylation* / drug effects
  • Ethnicity / genetics
  • Evidence-Based Practice
  • Female
  • Follow-Up Studies
  • Healthy Aging / genetics
  • Healthy Aging / psychology*
  • Humans
  • Male
  • Middle Aged
  • Motivation*
  • Repressor Proteins / genetics
  • Repressor Proteins / physiology*
  • Single-Blind Method
  • Smoking Cessation* / psychology

Substances

  • AHRR protein, human
  • Basic Helix-Loop-Helix Transcription Factors
  • Biomarkers
  • Repressor Proteins
  • Cotinine