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Table 1 Overview of various measures of epigenetic age acceleration and mortality risk used in this analysis

From: Epigenetic biomarkers of ageing are predictive of mortality risk in a longitudinal clinical cohort of individuals diagnosed with oropharyngeal cancer

Epigenetic marker

Abbreviation

CpGs

Description

References

Intrinsic Epigenetic age acceleration based on Horvath

IEAA

353

The residual resulting from regressing DNAm age on chronological age and estimates of major blood immune cell counts *

[26]

Intrinsic epigenetic age acceleration based on Hannum

IEAAHannum

71

 

[27]

Extrinsic age acceleration based on Hannum

EEAA

71

The residual resulting from a univariate model regressing a weighted age estimate (which increases the contribution of 3 cell types known to change with age **) on chronological age

[21]

Age acceleration based on PhenoAge

AgeAccelPheno

513

The residual resulting from a linear model when regressing PhenoAgeAccel on chronological age, where PhenoAge is an ageing measure based on a linear combination of chronological age and nine clinical biomarkers

[34]

Age acceleration based on GrimAge

AgeAccelGrim

1030

The residual resulting from a linear model when regressing GrimAge on chronological age, where GrimAge is an ageing measure based on a linear combination of chronological age, sex and DNAm-based surrogate biomarkers for smoking pack-years (DNAmpackyears) and seven plasma protein levels

[35]

Mortality risk score based on Zhang

ZhangScore

8

A linear combination of LASSO regression coefficient weighted methylation values of the ten CpGs

[36]

  1. * Naive CD8 + T cells, exhausted CD8 + T cells, plasmablasts, CD4 + T cells, natural killer cells, monocytes and granulocytes. ** naïve (CD45RA + CCR7 +) cytotoxic T cells, exhausted (CD28-CD45RA-) cytotoxic T cells and plasmablasts