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GWAS Study

GWAS of epigenetic aging rates in blood reveals a critical role for TERT.

Lu AT, Xue L, Salfati EL et al.

29374233 PubMed ID
GWAS Study Type
9907 Participants
43 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LA
Lu AT
XL
Xue L
SE
Salfati EL
CB
Chen BH
FL
Ferrucci L
LD
Levy D
JR
Joehanes R
MJ
Murabito JM
KD
Kiel DP
TP
Tsai PC
YI
Yet I
BJ
Bell JT
MM
Mangino M
TT
Tanaka T
MA
McRae AF
MR
Marioni RE
VP
Visscher PM
WN
Wray NR
DI
Deary IJ
LM
Levine ME
QA
Quach A
AT
Assimes T
TP
Tsao PS
AD
Absher D
SJ
Stewart JD
LY
Li Y
RA
Reiner AP
HL
Hou L
BA
Baccarelli AA
WE
Whitsel EA
AA
Aviv A
CA
Cardona A
DF
Day FR
WN
Wareham NJ
PJ
Perry JRB
OK
Ong KK
RK
Raj K
LK
Lunetta KL
HS
Horvath S
Chapter II

Abstract

Summary of the research findings

DNA methylation age is an accurate biomarker of chronological age and predicts lifespan, but its underlying molecular mechanisms are unknown. In this genome-wide association study of 9907 individuals, we find gene variants mapping to five loci associated with intrinsic epigenetic age acceleration (IEAA) and gene variants in three loci associated with extrinsic epigenetic age acceleration (EEAA). Mendelian randomization analysis suggests causal influences of menarche and menopause on IEAA and lipoproteins on IEAA and EEAA. Variants associated with longer leukocyte telomere length (LTL) in the telomerase reverse transcriptase gene (TERT) paradoxically confer higher IEAA (P < 2.7 × 10-11). Causal modeling indicates TERT-specific and independent effects on LTL and IEAA. Experimental hTERT-expression in primary human fibroblasts engenders a linear increase in DNA methylation age with cell population doubling number. Together, these findings indicate a critical role for hTERT in regulating the epigenetic clock, in addition to its established role of compensating for cell replication-dependent telomere shortening.

8,393 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

9907
Total Participants
GWAS
Study Type
Yes
Replicated
1,023 African American individuals, 491 Hispanic individuals
Replication Participants
African American or Afro-Caribbean, European, Hispanic or Latin American
Ancestry
U.S., Australia, U.K., Italy
Recruitment Country
Chapter IV

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