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...
Autores principales: | , , , , , , |
---|---|
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 |