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Plasma proteomic signature of age in healthy humans

To characterize the proteomic signature of chronological age, 1,301 proteins were measured in plasma using the SOMAscan assay (SomaLogic, Boulder, CO, USA) in a population of 240 healthy men and women, 22–93 years old, who were disease‐ and treatment‐free and had no physical and cognitive impairment...

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Autores principales: Tanaka, Toshiko, Biancotto, Angelique, Moaddel, Ruin, Moore, Ann Zenobia, Gonzalez‐Freire, Marta, Aon, Miguel A., Candia, Julián, Zhang, Pingbo, Cheung, Foo, Fantoni, Giovanna, Semba, Richard D., Ferrucci, Luigi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156492/
https://www.ncbi.nlm.nih.gov/pubmed/29992704
http://dx.doi.org/10.1111/acel.12799
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author Tanaka, Toshiko
Biancotto, Angelique
Moaddel, Ruin
Moore, Ann Zenobia
Gonzalez‐Freire, Marta
Aon, Miguel A.
Candia, Julián
Zhang, Pingbo
Cheung, Foo
Fantoni, Giovanna
Semba, Richard D.
Ferrucci, Luigi
author_facet Tanaka, Toshiko
Biancotto, Angelique
Moaddel, Ruin
Moore, Ann Zenobia
Gonzalez‐Freire, Marta
Aon, Miguel A.
Candia, Julián
Zhang, Pingbo
Cheung, Foo
Fantoni, Giovanna
Semba, Richard D.
Ferrucci, Luigi
author_sort Tanaka, Toshiko
collection PubMed
description To characterize the proteomic signature of chronological age, 1,301 proteins were measured in plasma using the SOMAscan assay (SomaLogic, Boulder, CO, USA) in a population of 240 healthy men and women, 22–93 years old, who were disease‐ and treatment‐free and had no physical and cognitive impairment. Using a p ≤ 3.83 × 10(−5) significance threshold, 197 proteins were positively associated, and 20 proteins were negatively associated with age. Growth differentiation factor 15 (GDF15) had the strongest, positive association with age (GDF15; 0.018 ± 0.001, p = 7.49 × 10(−56)). In our sample, GDF15 was not associated with other cardiovascular risk factors such as cholesterol or inflammatory markers. The functional pathways enriched in the 217 age‐associated proteins included blood coagulation, chemokine and inflammatory pathways, axon guidance, peptidase activity, and apoptosis. Using elastic net regression models, we created a proteomic signature of age based on relative concentrations of 76 proteins that highly correlated with chronological age (r = 0.94). The generalizability of our findings needs replication in an independent cohort.
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spelling pubmed-61564922018-10-01 Plasma proteomic signature of age in healthy humans Tanaka, Toshiko Biancotto, Angelique Moaddel, Ruin Moore, Ann Zenobia Gonzalez‐Freire, Marta Aon, Miguel A. Candia, Julián Zhang, Pingbo Cheung, Foo Fantoni, Giovanna Semba, Richard D. Ferrucci, Luigi Aging Cell Original Article To characterize the proteomic signature of chronological age, 1,301 proteins were measured in plasma using the SOMAscan assay (SomaLogic, Boulder, CO, USA) in a population of 240 healthy men and women, 22–93 years old, who were disease‐ and treatment‐free and had no physical and cognitive impairment. Using a p ≤ 3.83 × 10(−5) significance threshold, 197 proteins were positively associated, and 20 proteins were negatively associated with age. Growth differentiation factor 15 (GDF15) had the strongest, positive association with age (GDF15; 0.018 ± 0.001, p = 7.49 × 10(−56)). In our sample, GDF15 was not associated with other cardiovascular risk factors such as cholesterol or inflammatory markers. The functional pathways enriched in the 217 age‐associated proteins included blood coagulation, chemokine and inflammatory pathways, axon guidance, peptidase activity, and apoptosis. Using elastic net regression models, we created a proteomic signature of age based on relative concentrations of 76 proteins that highly correlated with chronological age (r = 0.94). The generalizability of our findings needs replication in an independent cohort. John Wiley and Sons Inc. 2018-07-11 2018-10 /pmc/articles/PMC6156492/ /pubmed/29992704 http://dx.doi.org/10.1111/acel.12799 Text en © 2018 The Authors. Aging Cell published by the Anatomical Society and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Tanaka, Toshiko
Biancotto, Angelique
Moaddel, Ruin
Moore, Ann Zenobia
Gonzalez‐Freire, Marta
Aon, Miguel A.
Candia, Julián
Zhang, Pingbo
Cheung, Foo
Fantoni, Giovanna
Semba, Richard D.
Ferrucci, Luigi
Plasma proteomic signature of age in healthy humans
title Plasma proteomic signature of age in healthy humans
title_full Plasma proteomic signature of age in healthy humans
title_fullStr Plasma proteomic signature of age in healthy humans
title_full_unstemmed Plasma proteomic signature of age in healthy humans
title_short Plasma proteomic signature of age in healthy humans
title_sort plasma proteomic signature of age in healthy humans
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156492/
https://www.ncbi.nlm.nih.gov/pubmed/29992704
http://dx.doi.org/10.1111/acel.12799
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