The Effect of Dietary Antioxidant Supplementation in Patients with Glaucoma.

8-OHdG glaucoma oxidative stress supplement

Journal

Clinical ophthalmology (Auckland, N.Z.)
ISSN: 1177-5467
Titre abrégé: Clin Ophthalmol
Pays: New Zealand
ID NLM: 101321512

Informations de publication

Date de publication:
2021
Historique:
received: 04 04 2021
accepted: 18 05 2021
entrez: 11 6 2021
pubmed: 12 6 2021
medline: 12 6 2021
Statut: epublish

Résumé

Oxidative stress may be a risk factor for glaucoma, and many previous reports have suggested that antioxidants could be a promising treatment. Here, we investigated the effects of a novel supplement containing three food-derived antioxidants (hesperidin, crocetin, and This study had a prospective, single arm design. Thirty Japanese glaucoma patients were recruited and given 4 tablets with ample water twice a day for 8 weeks. The treatment was stopped, and the subjects were followed for an additional 8 weeks. We measured biological antioxidant potential (BAP) with a free radical analyzer. We also measured urinary 8-hydroxy-2'-deoxyguanosine (8-OHdG; a marker of oxidative DNA damage). Clinical laboratory data were measured in venous blood samples. Clinical parameters were also recorded. Comparisons used a one-way analysis of variance (ANOVA) followed by Dunnett's test. The 8-OHdG level was not reduced. We also divided the patients into groups with high or low oxidative stress. In patients with relatively high oxidative stress, the 8-OHdG level was significantly reduced at weeks 4, 8, 12, and 16 ( An 8-week oral course of antioxidant supplementation was effective in patients with a high oxidative stress level. Dietary supplementation could hold promise in the treatment of systemic oxidative stress-related diseases.

Identifiants

pubmed: 34113073
doi: 10.2147/OPTH.S314288
pii: 314288
pmc: PMC8183457
doi:

Types de publication

Case Reports Clinical Trial

Langues

eng

Pagination

2293-2300

Informations de copyright

© 2021 Himori et al.

Déclaration de conflit d'intérêts

Professor Toru Nakazawa reports grants from Wakamoto Pharmaceutical Co., Ltd. during the conduct of this study;  grants and personal fees from Santen Pharmaceutical Co., Ltd., Senju Pharmaceutical Co., Ltd., and Topcon Corporation, outside the submitted work;  grants from Nidek Co., Ltd.  This research was supported by Wakamoto Pharmaceutical Co., Ltd. The authors report no other conflicts of interest in this work.

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Auteurs

Noriko Himori (N)

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Maki Inoue Yanagimachi (M)

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Kazuko Omodaka (K)

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Ophthalmic Imaging and Information Analytics, Tohoku University Graduate School of Medicine, Sendai, Japan.

Yukihiro Shiga (Y)

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Satoru Tsuda (S)

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Hiroshi Kunikata (H)

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Retinal Disease Control, Tohoku University Graduate School of Medicine, Sendai, Japan.

Toru Nakazawa (T)

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Ophthalmic Imaging and Information Analytics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Retinal Disease Control, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Advanced Ophthalmic Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.

Classifications MeSH