Comparison of Glutathione, Retinol and α- and γ-Tocopherols Concentrations Between Children with and Without Epilepsy: A Single-Center Case-Control Study.

IF 2.7 3区 医学 Q3 NEUROSCIENCES
Izabela Szołtysek-Bołdys, Wioleta Zielińska-Danch, Łucja Gajowska, Ilona Kopyta, Beata Sarecka-Hujar
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引用次数: 0

Abstract

Background: Oxidative stress is associated with the pathogenesis of epilepsy. Long-term treatment with anti-seizure medications (ASMs) may reduce antioxidant levels, which consequently impairs the brain's ability to counteract oxidative damage. This study aimed to assess the concentrations of selected antioxidants (i.e., glutathione, retinol, and α- and γ-tocopherols) in children with epilepsy treated with polytherapy.

Methods: The study included 21 children with epilepsy treated with ≥2 ASMs for at least 6 months (mean age 7.1 ± 4.4 years) and 23 control children without epilepsy (mean age 7.4 ± 3.9 years). Both groups were recruited at the Department of Pediatric Neurology, the Medical University of Silesia in Katowice (Poland). The concentrations of glutathione, retinol, and α- and γ-tocopherols were determined in blood serum by HPLC. The antioxidant levels were compared between sex and age subgroups of individuals with epilepsy.

Results: In the group of individuals with epilepsy, the percentage of females was 38% and in the control group it was 30%. There were no differences in antioxidant levels between female and male individuals with epilepsy, nor between younger epileptic children (0-6 years) and older children (>6 years). Individuals with epilepsy had significantly lower glutathione levels than the control group (1.5 ± 0.3 µmol/L vs. 2.4 ± 1.2 µmol/L, respectively, p < 0.001). In turn, the ratios of both α-tocopherol/glutathione and γ-tocopherol/glutathione were higher in individuals with epilepsy than in the control group (p = 0.042 and p = 0.004, respectively). Individuals with epilepsy taking ASM combinations other than valproic acid (VPA) and levetiracetam (LEV) had a lower level of both retinol and glutathione than individuals on VPA and LEV treatment (for retinol 0.44 ± 0.13 µmol/L vs. 0.6 ± 0.1 µmol/L, respectively, p = 0.047, and for glutathione 1.3 ± 0.3 µmol/L vs. 1.8 ± 0.3 µmol/L, respectively, p = 0.003). In the individuals with epilepsy, the level of α-tocopherol decreased with age (r = -0.505, p = 0.019). In turn, in the control group, the levels of retinol and γ-tocopherol increased with age (r = 0.573, p = 0.004 and r = 0.461, p = 0.027, respectively).

Conclusions: Glutathione levels significantly differed between children with and without epilepsy. The concentration of α-tocopherol decreased with age in pediatric individuals with epilepsy. The levels of both retinol and glutathione were higher in individuals with epilepsy taking VPA and LEV treatment compared to individuals on ASMs combination other than VPA and LEV.

癫痫患儿与非癫痫患儿谷胱甘肽、视黄醇、α-和γ-生育酚浓度的比较:一项单中心病例对照研究
背景:氧化应激与癫痫的发病机制有关。长期服用抗癫痫药物(asm)可能会降低抗氧化水平,从而损害大脑抵抗氧化损伤的能力。本研究旨在评估接受综合治疗的癫痫患儿中选定抗氧化剂(即谷胱甘肽、视黄醇、α-和γ-生育酚)的浓度。方法:研究对象为21例≥2次asm治疗至少6个月的癫痫患儿(平均年龄7.1±4.4岁)和23例非癫痫患儿(平均年龄7.4±3.9岁)。两组都是在卡托维兹(波兰)西里西亚医科大学儿科神经内科招募的。采用高效液相色谱法测定血清中谷胱甘肽、视黄醇、α-和γ-生育酚的浓度。对不同性别和年龄的癫痫患者进行抗氧化水平的比较。结果:在癫痫个体组中,女性比例为38%,对照组为30%。抗氧化剂水平在女性和男性癫痫患者之间没有差异,在年龄较小的癫痫儿童(0-6岁)和年龄较大的儿童(0-6岁)之间也没有差异。癫痫患者的谷胱甘肽水平显著低于对照组(分别为1.5±0.3µmol/L和2.4±1.2µmol/L, p < 0.001)。癫痫患者α-生育酚/谷胱甘肽和γ-生育酚/谷胱甘肽比值均高于对照组(p = 0.042和p = 0.004)。除丙戊酸(VPA)和左乙拉西坦(LEV)外,ASM联合用药的癫痫患者视黄醇和谷胱甘肽水平均低于VPA和LEV组(视黄醇分别为0.44±0.13µmol/L vs. 0.6±0.1µmol/L, p = 0.047;谷胱甘肽分别为1.3±0.3µmol/L vs. 1.8±0.3µmol/L, p = 0.003)。癫痫患者α-生育酚水平随年龄增长而降低(r = -0.505, p = 0.019)。在对照组中,视黄醇和γ-生育酚水平随年龄增长而升高(r = 0.573, p = 0.004和r = 0.461, p = 0.027)。结论:谷胱甘肽水平在癫痫患儿和非癫痫患儿之间存在显著差异。α-生育酚浓度随儿童癫痫患者年龄的增长而下降。服用VPA和LEV的癫痫患者视黄醇和谷胱甘肽水平高于服用asm而非VPA和LEV的癫痫患者。
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来源期刊
Brain Sciences
Brain Sciences Neuroscience-General Neuroscience
CiteScore
4.80
自引率
9.10%
发文量
1472
审稿时长
18.71 days
期刊介绍: Brain Sciences (ISSN 2076-3425) is a peer-reviewed scientific journal that publishes original articles, critical reviews, research notes and short communications in the areas of cognitive neuroscience, developmental neuroscience, molecular and cellular neuroscience, neural engineering, neuroimaging, neurolinguistics, neuropathy, systems neuroscience, and theoretical and computational neuroscience. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files or software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
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