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Epigenetic prediction of complex traits and mortality in a cohort of individuals with oropharyngeal cancer.
Langdon, Ryan J; Beynon, Rhona A; Ingarfield, Kate; Marioni, Riccardo E; McCartney, Daniel L; Martin, Richard M; Ness, Andy R; Pawlita, Michael; Waterboer, Tim; Relton, Caroline; Thomas, Steven J; Richmond, Rebecca C.
Afiliación
  • Langdon RJ; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
  • Beynon RA; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • Ingarfield K; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
  • Marioni RE; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
  • McCartney DL; NIHR Bristol Biomedical Research Centre, University Hospitals Bristol and University of Bristol, Bristol, UK.
  • Martin RM; Centre for Trials Research, Neuadd Meirionnydd, Heath Park Way, Cardiff, UK.
  • Ness AR; Community Oral Health, University of Glasgow Dental School, Sauchiehall Street, Glasgow, UK.
  • Pawlita M; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, Scotland, EH4 2XU, UK.
  • Waterboer T; Medical Genetics Section, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.
  • Relton C; MRC Human Genetics Unit, Institute of Genetics and Molecular Medicine, University of Edinburgh, Western General Hospital, Crewe Road, Edinburgh, Scotland, EH4 2XU, UK.
  • Thomas SJ; Medical Genetics Section, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.
  • Richmond RC; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Clin Epigenetics ; 12(1): 58, 2020 04 22.
Article en En | MEDLINE | ID: mdl-32321578
BACKGROUND: DNA methylation (DNAm) variation is an established predictor for several traits. In the context of oropharyngeal cancer (OPC), where 5-year survival is ~ 65%, DNA methylation may act as a prognostic biomarker. We examined the accuracy of DNA methylation biomarkers of 4 complex exposure traits (alcohol consumption, body mass index [BMI], educational attainment and smoking status) in predicting all-cause mortality in people with OPC. RESULTS: DNAm predictors of alcohol consumption, BMI, educational attainment and smoking status were applied to 364 individuals with OPC in the Head and Neck 5000 cohort (HN5000; 19.6% of total OPC cases in the study), followed up for median 3.9 years; inter-quartile range (IQR) 3.3 to 5.2 years (time-to-event-death or censor). The proportion of phenotypic variance explained in each trait was as follows: 16.5% for alcohol consumption, 22.7% for BMI, 0.4% for educational attainment and 51.1% for smoking. We then assessed the relationship between each DNAm predictor and all-cause mortality using Cox proportional-hazard regression analysis. DNAm prediction of smoking was most consistently associated with mortality risk (hazard ratio [HR], 1.38 per standard deviation (SD) increase in smoking DNAm score; 95% confidence interval [CI] 1.04 to 1.83; P 0.025, in a model adjusted for demographic, lifestyle, health and biological variables). Finally, we examined the accuracy of each DNAm predictor of mortality. DNAm predictors explained similar levels of variance in mortality to self-reported phenotypes. Receiver operator characteristic (ROC) curves for the DNAm predictors showed a moderate discrimination of alcohol consumption (area under the curve [AUC] 0.63), BMI (AUC 0.61) and smoking (AUC 0.70) when predicting mortality. The DNAm predictor for education showed poor discrimination (AUC 0.57). Z tests comparing AUCs between self-reported phenotype ROC curves and DNAm score ROC curves did not show evidence for difference between the two (alcohol consumption P 0.41, BMI P 0.62, educational attainment P 0.49, smoking P 0.19). CONCLUSIONS: In the context of a clinical cohort of individuals with OPC, DNAm predictors for smoking, alcohol consumption, educational attainment and BMI exhibit similar predictive values for all-cause mortality compared to self-reported data. These findings may have translational utility in prognostic model development, particularly where phenotypic data are not available.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Consumo de Bebidas Alcohólicas / Neoplasias Orofaríngeas / Biomarcadores de Tumor / Metilación de ADN / Fumar Tabaco Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Epigenetics Año: 2020 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Consumo de Bebidas Alcohólicas / Neoplasias Orofaríngeas / Biomarcadores de Tumor / Metilación de ADN / Fumar Tabaco Tipo de estudio: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Epigenetics Año: 2020 Tipo del documento: Article