Abstract:
BACKGROUND:Telomere length and DNA methylation have been proposed as biological clock measures that track chronological age. Whether they change in tandem, or contribute independently to the prediction of chronological age, is not known. METHODS:We address these points using data from two Scottish cohorts: the Lothian Birth Cohorts of 1921 (LBC1921) and 1936 (LBC1936). Telomere length and epigenetic clock estimates from DNA methylation were measured in 920 LBC1936 participants (ages 70, 73 and 76 years) and in 414 LBC1921 participants (ages 79, 87 and 90 years). RESULTS:The epigenetic clock changed over time at roughly the same rate as chronological age in both cohorts. Telomere length decreased at 48-67 base pairs per year on average. Weak, non-significant correlations were found between epigenetic clock estimates and telomere length. Telomere length explained 6.6% of the variance in age in LBC1921, the epigenetic clock explained 10.0%, and combined they explained 17.3% (allP< 1 × 10-7). Corresponding figures for the LBC1936 cohort were 14.3%, 11.7% and 19.5% (allP< 1 × 10-12). In a combined cohorts analysis, the respective estimates were 2.8%, 28.5% and 29.5%. Also in a combined cohorts analysis, a one standard deviation increase in baseline epigenetic age was linked to a 22% increased mortality risk (P= 2.6 × 10-4) whereas, in the same model, a one standard deviation increase in baseline telomere length was independently linked to an 11% decreased mortality risk (P= 0.06). CONCLUSIONS:These results suggest that telomere length and epigenetic clock estimates are independent predictors of chronological age and mortality risk.
journal_name
Int J Epidemioljournal_title
International journal of epidemiologyauthors
Marioni RE,Harris SE,Shah S,McRae AF,von Zglinicki T,Martin-Ruiz C,Wray NR,Visscher PM,Deary IJdoi
10.1093/ije/dyw041subject
Has Abstractpub_date
2018-02-01 00:00:00pages
424-432issue
2eissn
0300-5771issn
1464-3685pii
dyw041journal_volume
45pub_type
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