@article{8c43b4c5e9614523a5b231711317ac08,
title = "Proteomic assessment of serum biomarkers of longevity in older men",
abstract = "The biological bases of longevity are not well understood, and there are limited biomarkers for the prediction of long life. We used a high-throughput, discovery-based proteomics approach to identify serum peptides and proteins that were associated with the attainment of longevity in a longitudinal study of community-dwelling men age ≥65 years. Baseline serum in 1196 men were analyzed using liquid chromatography–ion mobility–mass spectrometry, and lifespan was determined during ~12 years of follow-up. Men who achieved longevity (≥90% expected survival) were compared to those who died earlier. Rigorous statistical methods that controlled for false positivity were utilized to identify 25 proteins that were associated with longevity. All these proteins were in lower abundance in long-lived men and included a variety involved in inflammation or complement activation. Lower levels of longevity-associated proteins were also associated with better health status, but as time to death shortened, levels of these proteins increased. Pathway analyses implicated a number of compounds as important upstream regulators of the proteins and implicated shared networks that underlie the observed associations with longevity. Overall, these results suggest that complex pathways, prominently including inflammation, are linked to the likelihood of attaining longevity. This work may serve to identify novel biomarkers for longevity and to understand the biology underlying lifespan.",
keywords = "aging, biomarker, inflammation, longevity, men, proteomics",
author = "{for the Osteoporotic Fractures in Men Study (MrOS) Research Group} and Orwoll, {Eric S.} and Jack Wiedrick and Nielson, {Carrie M.} and Jon Jacobs and Baker, {Erin S.} and Paul Piehowski and Vladislav Petyuk and Yuqian Gao and Tujin Shi and Smith, {Richard D.} and Bauer, {Douglas C.} and Cummings, {Steven R.} and Jodi Lapidus",
note = "Funding Information: The MrOS Study is supported by the following institutes under the National Institutes of Health (NIH): National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institute on Aging (NIA), National Center for Advancing Translational. Sciences (NCATS), and NIH roadmap for Medical Research under the following grant numbers: U01AR45580, U01AR45614, U01AR45632, U01AR 45647, U01AR45654, U01AR45583, U01AG18197, U01AG027810, and UL1RR024140, P50 AR063043, and endowment to the Center of Musculoskeletal health, UC Davis. The proteomics measurements were supported by the National Institutes of Health (NIH) NIGMS Grant P41 GM103493 (RDS) and were performed in the Environmental Molecular Science Laboratory, a U.S. Department of Energy (DOE) national scientific user facility at Pacific Northwest National Laboratory (PNNL) in Richland, WA. PNNL is operated by Battelle for the DOE under Contract DE‐AC05‐76RL0 1830. Proteome data analysis was further supported by the preceding grant as well as NIH/NCATS grant UL1TR000128. CMN was supported by K01 AR062655. Funding Information: The MrOS Study is supported by the following institutes under the National Institutes of Health (NIH): National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institute on Aging (NIA), National Center for Advancing Translational. Sciences (NCATS), and NIH roadmap for Medical Research under the following grant numbers: U01AR45580, U01AR45614, U01AR45632, U01AR 45647, U01AR45654, U01AR45583, U01AG18197, U01AG027810, and UL1RR024140, P50 AR063043, and endowment to the Center of Musculoskeletal health, UC Davis. The proteomics measurements were supported by the National Institutes of Health (NIH) NIGMS Grant P41 GM103493 (RDS) and were performed in the Environmental Molecular Science Laboratory, a U.S. Department of Energy (DOE) national scientific user facility at Pacific Northwest National Laboratory (PNNL) in Richland, WA. PNNL is operated by Battelle for the DOE under Contract DE-AC05-76RL0 1830. Proteome data analysis was further supported by the preceding grant as well as NIH/NCATS grant UL1TR000128. CMN was supported by K01 AR062655. Publisher Copyright: {\textcopyright} 2020 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd",
year = "2020",
month = nov,
doi = "10.1111/acel.13253",
language = "English (US)",
volume = "19",
journal = "Aging Cell",
issn = "1474-9718",
publisher = "Wiley-Blackwell",
number = "11",
}