Cargando…
Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study
Metabolites in human biofluids document the physiological status of individuals. We conducted comprehensive, non‐targeted, non‐invasive metabolomic analysis of urine from 27 healthy human subjects, comprising 13 young adults (30 ± 3 years) and 14 seniors (76 ± 4 years). Quantitative analysis of 99 m...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734427/ https://www.ncbi.nlm.nih.gov/pubmed/33336159 http://dx.doi.org/10.1096/fba.2020-00047 |
_version_ | 1783622471284424704 |
---|---|
author | Teruya, Takayuki Goga, Haruhisa Yanagida, Mitsuhiro |
author_facet | Teruya, Takayuki Goga, Haruhisa Yanagida, Mitsuhiro |
author_sort | Teruya, Takayuki |
collection | PubMed |
description | Metabolites in human biofluids document the physiological status of individuals. We conducted comprehensive, non‐targeted, non‐invasive metabolomic analysis of urine from 27 healthy human subjects, comprising 13 young adults (30 ± 3 years) and 14 seniors (76 ± 4 years). Quantitative analysis of 99 metabolites revealed 55 that displayed significant differences in abundance between the two groups. Forty‐four did not show a statistically significant relationship with age. These include 13 standard amino acids, 5 methylated, 4 acetylated, and 9 other amino acids, 6 nucleosides, nucleobases, and derivatives, 4 sugar derivatives, 5 sugar phosphates, 4 carnitines, 2 hydroxybutyrates, 1 choline, and 1 ethanolamine derivative, and glutathione disulfide. Abundances of 53 compounds decreased, while 2 (glutathione disulfide, myo‐inositol) increased in elderly people. The great majority of age‐linked markers were highly correlated with creatinine. In contrast, 44 other urinary metabolites, including urate, carnitine, hippurate, and betaine, were not age‐linked, neither declining nor increasing in elderly subjects. As metabolite profiles of urine and blood are quite different, age‐related information in urine offers additional valuable insights into aging mechanisms of endocrine system. Correlation analysis of urinary metabolites revealed distinctly inter‐related groups of compounds. |
format | Online Article Text |
id | pubmed-7734427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77344272020-12-16 Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study Teruya, Takayuki Goga, Haruhisa Yanagida, Mitsuhiro FASEB Bioadv Research Articles Metabolites in human biofluids document the physiological status of individuals. We conducted comprehensive, non‐targeted, non‐invasive metabolomic analysis of urine from 27 healthy human subjects, comprising 13 young adults (30 ± 3 years) and 14 seniors (76 ± 4 years). Quantitative analysis of 99 metabolites revealed 55 that displayed significant differences in abundance between the two groups. Forty‐four did not show a statistically significant relationship with age. These include 13 standard amino acids, 5 methylated, 4 acetylated, and 9 other amino acids, 6 nucleosides, nucleobases, and derivatives, 4 sugar derivatives, 5 sugar phosphates, 4 carnitines, 2 hydroxybutyrates, 1 choline, and 1 ethanolamine derivative, and glutathione disulfide. Abundances of 53 compounds decreased, while 2 (glutathione disulfide, myo‐inositol) increased in elderly people. The great majority of age‐linked markers were highly correlated with creatinine. In contrast, 44 other urinary metabolites, including urate, carnitine, hippurate, and betaine, were not age‐linked, neither declining nor increasing in elderly subjects. As metabolite profiles of urine and blood are quite different, age‐related information in urine offers additional valuable insights into aging mechanisms of endocrine system. Correlation analysis of urinary metabolites revealed distinctly inter‐related groups of compounds. John Wiley and Sons Inc. 2020-10-21 /pmc/articles/PMC7734427/ /pubmed/33336159 http://dx.doi.org/10.1096/fba.2020-00047 Text en © 2020 The Authors. FASEB BioAdvances published by the Federation of American Societies for Experimental Biology This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Teruya, Takayuki Goga, Haruhisa Yanagida, Mitsuhiro Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study |
title | Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study |
title_full | Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study |
title_fullStr | Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study |
title_full_unstemmed | Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study |
title_short | Aging markers in human urine: A comprehensive, non‐targeted LC‐MS study |
title_sort | aging markers in human urine: a comprehensive, non‐targeted lc‐ms study |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7734427/ https://www.ncbi.nlm.nih.gov/pubmed/33336159 http://dx.doi.org/10.1096/fba.2020-00047 |
work_keys_str_mv | AT teruyatakayuki agingmarkersinhumanurineacomprehensivenontargetedlcmsstudy AT gogaharuhisa agingmarkersinhumanurineacomprehensivenontargetedlcmsstudy AT yanagidamitsuhiro agingmarkersinhumanurineacomprehensivenontargetedlcmsstudy |