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Metabolite signatures of chronological age, aging, survival, and longevity.

Authors :
Sebastiani P
Monti S
Lustgarten MS
Song Z
Ellis D
Tian Q
Schwaiger-Haber M
Stancliffe E
Leshchyk A
Short MI
Ardisson Korat AV
Gurinovich A
Karagiannis T
Li M
Lords HJ
Xiang Q
Marron MM
Bae H
Feitosa MF
Wojczynski MK
O'Connell JR
Montasser ME
Schupf N
Arbeev K
Yashin A
Schork N
Christensen K
Andersen SL
Ferrucci L
Rappaport N
Perls TT
Patti GJ
Source :
Cell reports [Cell Rep] 2024 Nov 26; Vol. 43 (11), pp. 114913. Date of Electronic Publication: 2024 Nov 05.
Publication Year :
2024

Abstract

Metabolites that mark aging are not fully known. We analyze 408 plasma metabolites in Long Life Family Study participants to characterize markers of age, aging, extreme longevity, and mortality. We identify 308 metabolites associated with age, 258 metabolites that change over time, 230 metabolites associated with extreme longevity, and 152 metabolites associated with mortality risk. We replicate many associations in independent studies. By summarizing the results into 19 signatures, we differentiate between metabolites that may mark aging-associated compensatory mechanisms from metabolites that mark cumulative damage of aging and from metabolites that characterize extreme longevity. We generate and validate a metabolomic clock that predicts biological age. Network analysis of the age-associated metabolites reveals a critical role of essential fatty acids to connect lipids with other metabolic processes. These results characterize many metabolites involved in aging and point to nutrition as a source of intervention for healthy aging therapeutics.<br />Competing Interests: Declaration of interests M.E.M. receives research funding unrelated to this work from Regeneron Pharmaceutical Inc.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
2211-1247
Volume :
43
Issue :
11
Database :
MEDLINE
Journal :
Cell reports
Publication Type :
Academic Journal
Accession number :
39504246
Full Text :
https://doi.org/10.1016/j.celrep.2024.114913