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Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage

Systemic oxidative stress is thought to be an important factor in the pathogenesis of glaucoma. In particular, low systemic antioxidative capacity, which normally counters oxidative stress, may contribute to glaucoma. Thus, we investigated the association between biological antioxidant potential (BA...

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Autores principales: Asano, Yoshimi, Himori, Noriko, Kunikata, Hiroshi, Yamazaki, Mai, Shiga, Yukihiro, Omodaka, Kazuko, Takahashi, Hidetoshi, Nakazawa, Toru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556047/
https://www.ncbi.nlm.nih.gov/pubmed/28808277
http://dx.doi.org/10.1038/s41598-017-08624-4
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author Asano, Yoshimi
Himori, Noriko
Kunikata, Hiroshi
Yamazaki, Mai
Shiga, Yukihiro
Omodaka, Kazuko
Takahashi, Hidetoshi
Nakazawa, Toru
author_facet Asano, Yoshimi
Himori, Noriko
Kunikata, Hiroshi
Yamazaki, Mai
Shiga, Yukihiro
Omodaka, Kazuko
Takahashi, Hidetoshi
Nakazawa, Toru
author_sort Asano, Yoshimi
collection PubMed
description Systemic oxidative stress is thought to be an important factor in the pathogenesis of glaucoma. In particular, low systemic antioxidative capacity, which normally counters oxidative stress, may contribute to glaucoma. Thus, we investigated the association between biological antioxidant potential (BAP), a biomarker of systemic antioxidative capacity, and glaucoma severity in patients with open-angle glaucoma (OAG). This study included 480 eyes of 240 patients with OAG and 66 healthy control eyes. We measured the BAP serum level with a free radical analyzer and compared it with a weighted estimate of the number of retinal ganglion cells (wrgc), derived from circumpapillary retinal nerve fiber layer thickness and visual field mean deviation. We found that wrgc was uncorrelated with BAP in the overall, male, and female OAG patients, but was correlated in young (aged ≤ 65 years) male OAG patients (better eye: r = 0.33, P = 0.02; worse eye: r = 0.27, P = 0.047). Furthermore, a mixed-effects regression analysis revealed that BAP was an independent contributing factor to wrgc in young male OAG patients (P = 0.02). Thus, systemic antioxidant capacity was associated with glaucomatous damage in relatively young male patients, suggesting that anti-oxidant therapy might be more effective in these patients.
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spelling pubmed-55560472017-08-16 Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage Asano, Yoshimi Himori, Noriko Kunikata, Hiroshi Yamazaki, Mai Shiga, Yukihiro Omodaka, Kazuko Takahashi, Hidetoshi Nakazawa, Toru Sci Rep Article Systemic oxidative stress is thought to be an important factor in the pathogenesis of glaucoma. In particular, low systemic antioxidative capacity, which normally counters oxidative stress, may contribute to glaucoma. Thus, we investigated the association between biological antioxidant potential (BAP), a biomarker of systemic antioxidative capacity, and glaucoma severity in patients with open-angle glaucoma (OAG). This study included 480 eyes of 240 patients with OAG and 66 healthy control eyes. We measured the BAP serum level with a free radical analyzer and compared it with a weighted estimate of the number of retinal ganglion cells (wrgc), derived from circumpapillary retinal nerve fiber layer thickness and visual field mean deviation. We found that wrgc was uncorrelated with BAP in the overall, male, and female OAG patients, but was correlated in young (aged ≤ 65 years) male OAG patients (better eye: r = 0.33, P = 0.02; worse eye: r = 0.27, P = 0.047). Furthermore, a mixed-effects regression analysis revealed that BAP was an independent contributing factor to wrgc in young male OAG patients (P = 0.02). Thus, systemic antioxidant capacity was associated with glaucomatous damage in relatively young male patients, suggesting that anti-oxidant therapy might be more effective in these patients. Nature Publishing Group UK 2017-08-14 /pmc/articles/PMC5556047/ /pubmed/28808277 http://dx.doi.org/10.1038/s41598-017-08624-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Asano, Yoshimi
Himori, Noriko
Kunikata, Hiroshi
Yamazaki, Mai
Shiga, Yukihiro
Omodaka, Kazuko
Takahashi, Hidetoshi
Nakazawa, Toru
Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage
title Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage
title_full Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage
title_fullStr Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage
title_full_unstemmed Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage
title_short Age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage
title_sort age- and sex-dependency of the association between systemic antioxidant potential and glaucomatous damage
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556047/
https://www.ncbi.nlm.nih.gov/pubmed/28808277
http://dx.doi.org/10.1038/s41598-017-08624-4
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