2019
DOI: 10.1186/s13073-019-0667-1
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Improved precision of epigenetic clock estimates across tissues and its implication for biological ageing

Abstract: Background DNA methylation changes with age. Chronological age predictors built from DNA methylation are termed ‘epigenetic clocks’. The deviation of predicted age from the actual age (‘age acceleration residual’, AAR) has been reported to be associated with death. However, it is currently unclear how a better prediction of chronological age affects such association. Methods In this study, we build multiple predictors based on training DNA methylation samples selected f… Show more

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Cited by 218 publications
(243 citation statements)
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“…Prior to association analyses we regressed DNA methylation measures on known batch effects, which included sentrix row, column and slide in SGPD, and sentrix row and column only in PEG, because slide was significantly associated with disease status in that sample. Sex, predicted age 55 , predicted smoking exposure (unpublished work) and predicted CTPs (with the exception of eosinophils) were fitted as fixed effects. We checked strongly associated probes for the presence of common SNPs, using the masking manifests provided by Illumina (https://zwdzwd.github.io/InfiniumAnnotation).…”
Section: Discussionmentioning
confidence: 99%
“…Prior to association analyses we regressed DNA methylation measures on known batch effects, which included sentrix row, column and slide in SGPD, and sentrix row and column only in PEG, because slide was significantly associated with disease status in that sample. Sex, predicted age 55 , predicted smoking exposure (unpublished work) and predicted CTPs (with the exception of eosinophils) were fitted as fixed effects. We checked strongly associated probes for the presence of common SNPs, using the masking manifests provided by Illumina (https://zwdzwd.github.io/InfiniumAnnotation).…”
Section: Discussionmentioning
confidence: 99%
“…Written consent was obtained from all individuals enrolled in this study, and the study was approved by the corresponding HREC at the different sites: University of Sydney, Western Sydney Local Health District, Royal Brisbane and Women Hospital Metro North, South Metropolitan Health Service, Macquarie University, QIMR Berghofer Medical Research Institute, University of New South Wales and the University of Melbourne. The mean predicted age, 40 predicted smoking scores, 29 and sex distribution between cases and controls for the cohorts used in this study can be found in Supplementary Table 5.…”
Section: Datasets Descriptionmentioning
confidence: 99%
“…In a wide-ranging review describing the development and evolution of the epigenetic clocks, Horvath & Raj 5 acknowledged that the first-generation clocks exhibited only weak associations with clinical measures of physiological dysregulation such as blood pressure or glucose metabolism that anticipate hard disease end-points. Recently, Zhang et al 8 have shown that, in principle, a near perfect predictor of calendar age can be estimated from DNA methylation levels, but its association with mortality attenuates with increased accuracy in predicting calendar age; the logical corollary of which is that the training sets being used for deriving accurate biological age estimators require more for their calibration than simply calendar age. The second-generation clocks, PhenoAge 9 and GrimAge 10 were designed to overcome these limitations by including DNAm correlates of morbidity and mortality.…”
Section: Mainmentioning
confidence: 99%