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Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging

Background: A molecular biomarker of physiologic age, as opposed to chronologic age, is needed in clinical medicine. 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodGsn) and 8-oxo-7, 8-dihydroguanosine (8-oxoGsn) are two promising aging biomarkers. Methods: A total of 1,228 healthy Chinese residents (613...

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Autores principales: Gan, Wei, Liu, Xin-Le, Yu, Ting, Zou, Yuan-Gao, Li, Ting-Ting, Wang, Shuang, Deng, Jin, Wang, Lan-Lan, Cai, Jian-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835306/
https://www.ncbi.nlm.nih.gov/pubmed/29535624
http://dx.doi.org/10.3389/fnagi.2018.00034
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author Gan, Wei
Liu, Xin-Le
Yu, Ting
Zou, Yuan-Gao
Li, Ting-Ting
Wang, Shuang
Deng, Jin
Wang, Lan-Lan
Cai, Jian-Ping
author_facet Gan, Wei
Liu, Xin-Le
Yu, Ting
Zou, Yuan-Gao
Li, Ting-Ting
Wang, Shuang
Deng, Jin
Wang, Lan-Lan
Cai, Jian-Ping
author_sort Gan, Wei
collection PubMed
description Background: A molecular biomarker of physiologic age, as opposed to chronologic age, is needed in clinical medicine. 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodGsn) and 8-oxo-7, 8-dihydroguanosine (8-oxoGsn) are two promising aging biomarkers. Methods: A total of 1,228 healthy Chinese residents (613 males and 615 females) 2–90 years of age were randomly selected. Spot urine samples were collected, and the concentrations of 8-oxodGsn and 8-oxoGsn were measured using ultra-high-performance liquid chromatography with a triple quadrupole mass spectrometer (UPLC-MS/MS). Method validation, including accuracy, precision, linearity and quantification limit, was performed. The relationship between oxidized guanosine and age/gender was evaluated. Results: 8-oxodGsn and 8-oxoGsn were eluted at 1.61 and 1.30 min, respectively. The calibration curve was linear in the range of 0.2–500 ng/ml for both analytes. The lowest limit of quantification (LLOQ) was 0.2 ng/ml for 8-oxodGsn and 0.1 ng/ml for 8-oxoGsn. There was an age-dependent increase in the biomarkers from the 21- to 30-year-old group to the 81- to 90-year-old group in both genders. In the subjects older than 61 years of age, the levels of 8-oxodGsn as well as 8-oxoGsn in urine were much higher in females than in males. The content of 8-oxoGsn correlated more closely with age and was higher (approximately 2-fold) than that of 8-oxodGsn for a given individual. Conclusions: 8-oxodGsn and 8-oxoGsn can be easily measured by UPLC-MS/MS. Urinary 8-oxoGsn may be a potential biomarker to determine a person's physiologic age and identify individuals at high risk of developing age-associated disease.
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spelling pubmed-58353062018-03-13 Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging Gan, Wei Liu, Xin-Le Yu, Ting Zou, Yuan-Gao Li, Ting-Ting Wang, Shuang Deng, Jin Wang, Lan-Lan Cai, Jian-Ping Front Aging Neurosci Neuroscience Background: A molecular biomarker of physiologic age, as opposed to chronologic age, is needed in clinical medicine. 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodGsn) and 8-oxo-7, 8-dihydroguanosine (8-oxoGsn) are two promising aging biomarkers. Methods: A total of 1,228 healthy Chinese residents (613 males and 615 females) 2–90 years of age were randomly selected. Spot urine samples were collected, and the concentrations of 8-oxodGsn and 8-oxoGsn were measured using ultra-high-performance liquid chromatography with a triple quadrupole mass spectrometer (UPLC-MS/MS). Method validation, including accuracy, precision, linearity and quantification limit, was performed. The relationship between oxidized guanosine and age/gender was evaluated. Results: 8-oxodGsn and 8-oxoGsn were eluted at 1.61 and 1.30 min, respectively. The calibration curve was linear in the range of 0.2–500 ng/ml for both analytes. The lowest limit of quantification (LLOQ) was 0.2 ng/ml for 8-oxodGsn and 0.1 ng/ml for 8-oxoGsn. There was an age-dependent increase in the biomarkers from the 21- to 30-year-old group to the 81- to 90-year-old group in both genders. In the subjects older than 61 years of age, the levels of 8-oxodGsn as well as 8-oxoGsn in urine were much higher in females than in males. The content of 8-oxoGsn correlated more closely with age and was higher (approximately 2-fold) than that of 8-oxodGsn for a given individual. Conclusions: 8-oxodGsn and 8-oxoGsn can be easily measured by UPLC-MS/MS. Urinary 8-oxoGsn may be a potential biomarker to determine a person's physiologic age and identify individuals at high risk of developing age-associated disease. Frontiers Media S.A. 2018-02-27 /pmc/articles/PMC5835306/ /pubmed/29535624 http://dx.doi.org/10.3389/fnagi.2018.00034 Text en Copyright © 2018 Gan, Liu, Yu, Zou, Li, Wang, Deng, Wang and Cai. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Gan, Wei
Liu, Xin-Le
Yu, Ting
Zou, Yuan-Gao
Li, Ting-Ting
Wang, Shuang
Deng, Jin
Wang, Lan-Lan
Cai, Jian-Ping
Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging
title Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging
title_full Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging
title_fullStr Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging
title_full_unstemmed Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging
title_short Urinary 8-oxo-7,8-dihydroguanosine as a Potential Biomarker of Aging
title_sort urinary 8-oxo-7,8-dihydroguanosine as a potential biomarker of aging
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5835306/
https://www.ncbi.nlm.nih.gov/pubmed/29535624
http://dx.doi.org/10.3389/fnagi.2018.00034
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