Cargando…

MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558

Biological age (BA) has been shown to be a better predictor of mortality and disease than chronological age (CA). Aging’s diverse effects are visible across many data types. We investigated BA from deep phenotyping of 3558 wellness program participants and controls. The Klemera-Doubal BA estimation...

Descripción completa

Detalles Bibliográficos
Autores principales: Price, Nathan, Earls, John, Rappaport, Noa, Heath, Laura, Wilmanski, Tomasz, Lovejoy, Jennifer, Hood, Leroy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845313/
http://dx.doi.org/10.1093/geroni/igz038.761
_version_ 1783468636273377280
author Price, Nathan
Price, Nathan
Earls, John
Rappaport, Noa
Heath, Laura
Wilmanski, Tomasz
Lovejoy, Jennifer
Hood, Leroy
author_facet Price, Nathan
Price, Nathan
Earls, John
Rappaport, Noa
Heath, Laura
Wilmanski, Tomasz
Lovejoy, Jennifer
Hood, Leroy
author_sort Price, Nathan
collection PubMed
description Biological age (BA) has been shown to be a better predictor of mortality and disease than chronological age (CA). Aging’s diverse effects are visible across many data types. We investigated BA from deep phenotyping of 3558 wellness program participants and controls. The Klemera-Doubal BA estimation algorithm was applied to genetic and longitudinal clinical laboratory, metabolomic, and proteomic assay data. BA trajectories were calculated using Generalized Estimating Equations. BA of individuals with Type-2 Diabetes averaged 6+ years greater than CA. Wellness program participation decreased individuals’ rate of aging (coefficient: -0.16, 95% CI: -0.45, 0.19), with effects dependent on sex, initial BA, and CA. Measures of metabolic health, inflammation, and toxin bioaccumulation were strong predictors across data types and sex. Deep phenotyping enabled calculation of a BA measure and a wellness program improved BA, either in absolute terms or relative to CA, showing it is modifiable.
format Online
Article
Text
id pubmed-6845313
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-68453132019-11-18 MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558 Price, Nathan Price, Nathan Earls, John Rappaport, Noa Heath, Laura Wilmanski, Tomasz Lovejoy, Jennifer Hood, Leroy Innov Aging Session 1120 (Symposium) Biological age (BA) has been shown to be a better predictor of mortality and disease than chronological age (CA). Aging’s diverse effects are visible across many data types. We investigated BA from deep phenotyping of 3558 wellness program participants and controls. The Klemera-Doubal BA estimation algorithm was applied to genetic and longitudinal clinical laboratory, metabolomic, and proteomic assay data. BA trajectories were calculated using Generalized Estimating Equations. BA of individuals with Type-2 Diabetes averaged 6+ years greater than CA. Wellness program participation decreased individuals’ rate of aging (coefficient: -0.16, 95% CI: -0.45, 0.19), with effects dependent on sex, initial BA, and CA. Measures of metabolic health, inflammation, and toxin bioaccumulation were strong predictors across data types and sex. Deep phenotyping enabled calculation of a BA measure and a wellness program improved BA, either in absolute terms or relative to CA, showing it is modifiable. Oxford University Press 2019-11-08 /pmc/articles/PMC6845313/ http://dx.doi.org/10.1093/geroni/igz038.761 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Session 1120 (Symposium)
Price, Nathan
Price, Nathan
Earls, John
Rappaport, Noa
Heath, Laura
Wilmanski, Tomasz
Lovejoy, Jennifer
Hood, Leroy
MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558
title MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558
title_full MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558
title_fullStr MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558
title_full_unstemmed MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558
title_short MULTI-OMIC BIOLOGICAL AGE ESTIMATION, CORRELATION WITH WELLNESS, DISEASE PHENOTYPES: LONGITUDINAL SAMPLE OF 3558
title_sort multi-omic biological age estimation, correlation with wellness, disease phenotypes: longitudinal sample of 3558
topic Session 1120 (Symposium)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845313/
http://dx.doi.org/10.1093/geroni/igz038.761
work_keys_str_mv AT pricenathan multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558
AT pricenathan multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558
AT earlsjohn multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558
AT rappaportnoa multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558
AT heathlaura multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558
AT wilmanskitomasz multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558
AT lovejoyjennifer multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558
AT hoodleroy multiomicbiologicalageestimationcorrelationwithwellnessdiseasephenotypeslongitudinalsampleof3558