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Journal ArticleDOI

Vitamin E supplementation in chronically hemodialyzed patients - influence on blood hemoglobin and plasma (anti)oxidant status.

TLDR
When treated with ESA and iron on a long-term basis, the response to the vitamin E supplementation in chronically hemodialyzed patients is largely dependent on their basal blood hemoglobin and serum vitamin E concentrations.
Abstract
Background: Disturbed oxidant/antioxidant status is involved in pathogenesis of anemia in end stage renal disease. There is evidence that vitamin E supplementation can increase blood hemoglobin in chronically hemodialyzed patients. However, the interindividual variation in response to the supplementation has not been fully addressed. Methods: 24 chronically hemodialyzed patients were supplemented with vitamin E (400 IU/day) in a period of two months. They had already been treated with erythropoiesis stimulating agents (ESA) and iron on a long-term basis, which was continued during the study period. A group of 20 healthy volunteers served as control subjects. Complete blood count, general biochemistry assays, the redox status by total thiols, oxidative stress by reactive oxygen metabolites, antioxidant status by biological antioxidant potential, and vitamin E (α- and γ- tocopherol) were measured before the start of supplementation, one month and two months later. Results: Overall, the vitamin E supplementation did not cause an increase of blood hemoglobin, hematocrit or red blood cells. However, 50 % of the patients with basal blood hemoglobin below 12.0 g/dL (N = 10) responded to the supplementation with its continuous increase. In addition, vitamin E exhibited a slight prooxidant effect only in the subgroup of patients with basal blood hemoglobin of ≥ 12.0 g/dL, two months after the start of supplementation (decreased total thiols: 300 ± 31 vs. 277 ± 36 µmol/L, p 0.05; decreased biological antioxidant potential: 2278 ± 150 vs. 2171 ± 126 µEq/L, p < 0.025), which coincided with their significantly increased serum α-tocopherol concentrations in comparison to the patients with basal blood hemoglobin below 12.0 g/dL (41.3 ± 7.2 vs. 59.9 ± 19.2 µmol/L, p < 0.025). Conclusions: When treated with ESA and iron on a long-term basis, the response to the vitamin E supplementation in chronically hemodialyzed patients is largely dependent on their basal blood hemoglobin and serum vitamin E concentrations.

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Polyphenols in human nutrition: from the in vitro antioxidant capacity to the beneficial effects on cardiometabolic health and related inter-individual variability - an overview and perspective.

TL;DR: The phenomenon of inter-individual variability in response to consumption of polyphenols is of relevance for supplementation with antioxidant (pro)vitamins and will potentially lead to personalised dietary recommendations.
Journal ArticleDOI

Circadian rhythm and time-of-day-effects of (anti)oxidant biomarkers for epidemiological studies.

TL;DR: Diurnal variations in some of the studied biomarkers of oxidative stress, redox and antioxidant status in serum/plasma should be taken into account when designing and conducting clinical and epidemiological studies.
References
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Journal ArticleDOI

Antioxidant and prooxidant activity of (alpha)-tocopherol in human plasma and low density lipoprotein

TL;DR: The results indicate that the level of oxidative stress and concentration of co-antioxidants, such as ascorbate, capable of regenerating alpha-tocopherol in the oxidizing lipoprotein particle, appear to represent major factors determining alpha-ocopherol activity towards oxidation both in human plasma and LDL.
Journal ArticleDOI

Suicidal erythrocyte death in end-stage renal disease

TL;DR: Both, dialyzable components of uremic plasma and dialysis procedure, trigger eryptosis at least in part by increasing erythrocyte [Ca2+]i, ROS, and ceramide formation.
Journal ArticleDOI

Antioxidants for chronic kidney disease

TL;DR: Antioxidant therapy was found to significantly reduce development of end-stage of kidney disease (ESKD) and lower serum creatinine levels and there was significant heterogeneity for cardiovascular disease when studies were analysed by CKD stage.
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