Epigenetic modelling of former, current and never smokers

Ryan J Langdon*, Paul D Yousefi, Caroline L Relton, Matthew J Suderman

*Corresponding author for this work

Research output: Contribution to journalArticle (Academic Journal)peer-review

14 Citations (Scopus)
69 Downloads (Pure)

Abstract

Background: DNA methylation (DNAm) performs excellently in the discrimination of current and former smokers from never smokers, where AUCs >0.9 are regularly reported using a single CpG site (cg05575921; AHRR). However, there is a paucity of DNAm models which attempt to distinguish current, former and never smokers as individual classes. Derivation of a robust DNAm model that accurately distinguishes between current, former and never smokers would be particularly valuable to epidemiological research (as a more accurate smoking definition vs self-report) and could potentially translate to clinical settings. Therefore, we appraise 4 DNAm models of ternary smoking status (that is, current, former and never smokers): methylation at cg05575921 (AHRR model), weighted scores from 13 CpGs created by Maas et al. (Maas model), weighted scores from a LASSO model of candidate smoking CpGs from literature (candidate CpG LASSO model), and weighted scores from a LASSO model supplied with genome-wide 450K data (agnostic LASSO model). Discrimination is assessed by AUC, whilst classification accuracy is assessed by accuracy and kappa, derived from confusion matrices.
Results: We find that DNAm can classify ternary smoking status with reasonable accuracy, including when applied to external data. Ternary classification using only DNAm far exceeds the classification accuracy of simply assigning all classes as the most prevalent class (63.7% vs 36.4%). Further, we develop a DNAm classifier which performs well in discriminating current from former smokers (agnostic LASSO model AUC in external validation data: 0.744). Finally, across our DNAm models, we show evidence of enrichment for biological pathways and human phenotype ontologies relevant to smoking, such as haemostasis, molybdenum cofactor synthesis, body fatness and social behaviours, providing evidence of the generalisability of our classifiers.
Conclusions: Our findings suggest that DNAm can classify ternary smoking status with close to 65% accuracy. Both the ternary smoking status classifiers and current vs former smoking status classifiers address the present lack of former smoker classification in epigenetic literature; essential if DNAm classifiers are to adequately relate to real-world populations. To improve performance further, additional focus on improving discrimination of current from former smokers is necessary.
Original languageEnglish
Article number206
Number of pages13
JournalClinical Epigenetics
Volume13
Issue number1
Early online date17 Nov 2021
DOIs
Publication statusPublished - Dec 2021

Bibliographical note

Funding Information:
We would like to thank the Center for Epigenetics at Johns Hopkins University School of Medicine (Liu et al.), the Environmental Genomics Group at the National Institute of Environmental Health Sciences in North Carolina (Su et al.), the Wellcome Trust Sanger Institute at Cambridge (Tsaprouni et al.) and the Gastrointestinal Unit at the Centre for Genomics and Molecular Medicine in Edinburgh (Ventham et al.) for making their epigenetic datasets and corresponding phenotypic information publicly available on the GEO Datasets database. We would also like to express our gratitude to all of the participants of the contributing studies to each of these datasets.

Funding Information:
RL, PY, CR and MS were supported by a Cancer Research UK (C18281/A29019) programme grant (the Integrative Cancer Epidemiology Programme), in addition to the UK Medical Research Council (MC_UU_00011/5), which funds the Integrative Epidemiology Unit at the University of Bristol, where RL, PY, MS and CR work.

Publisher Copyright:
© 2021, The Author(s).

Research Groups and Themes

  • ICEP

Keywords

  • Epigenetic
  • smoking
  • classification
  • methylation
  • epidemiology

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