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自闭症儿童氧化还原代谢异常与线粒体疾病有关。

Redox metabolism abnormalities in autistic children associated with mitochondrial disease.

机构信息

Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR, USA.

出版信息

Transl Psychiatry. 2013 Jun 18;3(6):e273. doi: 10.1038/tp.2013.51.

Abstract

Research studies have uncovered several metabolic abnormalities associated with autism spectrum disorder (ASD), including mitochondrial disease (MD) and abnormal redox metabolism. Despite the close connection between mitochondrial dysfunction and oxidative stress, the relation between MD and oxidative stress in children with ASD has not been studied. Plasma markers of oxidative stress and measures of cognitive and language development and ASD behavior were obtained from 18 children diagnosed with ASD who met criteria for probable or definite MD per the Morava et al. criteria (ASD/MD) and 18 age and gender-matched ASD children without any biological markers or symptoms of MD (ASD/NoMD). Plasma measures of redox metabolism included reduced free glutathione (fGSH), oxidized glutathione (GSSG), the fGSH/GSSG ratio and 3-nitrotyrosine (3NT). In addition, a plasma measure of chronic immune activation, 3-chlorotyrosine (3CT), was also measured. Language was measured using the preschool language scale or the expressive one-word vocabulary test (depending on the age), adaptive behaviour was measured using the Vineland Adaptive Behavior Scale (VABS) and core autism symptoms were measured using the Autism Symptoms Questionnaire and the Social Responsiveness Scale. Children with ASD/MD were found to have lower scores on the communication and daily living skill subscales of the VABS despite having similar language and ASD symptoms. Children with ASD/MD demonstrated significantly higher levels of fGSH/GSSG and lower levels of GSSG as compared with children with ASD/NoMD, suggesting an overall more favourable glutathione redox status in the ASD/MD group. However, compare with controls, both ASD groups demonstrated lower fGSH and fGSH/GSSG, demonstrating that both groups suffer from redox abnormalities. Younger ASD/MD children had higher levels of 3CT than younger ASD/NoMD children because of an age-related effect in the ASD/MD group. Both ASD groups demonstrated significantly higher 3CT levels than control subjects, suggesting that chronic inflammation was present in both groups of children with ASD. Interestingly, 3NT was found to correlate positively with several measures of cognitive function, development and behavior for the ASD/MD group, but not the ASD/NoMD group, such that higher 3NT concentrations were associated with more favourable adaptive behaviour, language and ASD-related behavior. To determine whether difference in receiving medications and/or supplements could account for the differences in redox and inflammatory biomarkers across ASD groups, we examined differences in medication and supplements across groups and their effect of redox and inflammatory biomarkers. Overall, significantly more participants in the ASD/MD group were receiving folate, vitamin B12, carnitine, co-enzyme Q10, B vitamins and antioxidants. We then determined whether folate, carnitine, co-enzyme Q10, B vitamins and/or antioxidants influenced redox or inflammatory biomarkers. Antioxidant supplementation was associated with a significantly lower GSSG, whereas antioxidants, co-enzyme Q10 and B vitamins were associated with a higher fGSH/GSSG ratio. There was no relation between folate, carnitine, co-enzyme Q10, B vitamins and antioxidants with 3NT, 3CT or fGSH. Overall, our findings suggest that ASD/MD children with a more chronic oxidized microenvironment have better development. We interpret this finding in light of the fact that more active mitochondrial can create a greater oxidized microenvironment especially when dysfunctional. Thus, compensatory upregulation of mitochondria which are dysfunctional may both increase activity and function at the expense of a more oxidized microenvironment. Although more ASD/MD children were receiving certain supplements, the use of such supplements were not found to be related to the redox biomarkers that were related to cognitive development or behavior in the ASD/MD group but could possibly account for the difference in glutathione metabolism noted between groups. This study suggests that different subgroups of children with ASD have different redox abnormalities, which may arise from different sources. A better understanding of the relationship between mitochondrial dysfunction in ASD and oxidative stress, along with other factors that may contribute to oxidative stress, will be critical to understanding how to guide treatment and management of ASD children. This study also suggests that it is important to identify ASD/MD children as they may respond differently to specific treatments because of their specific metabolic profile.

摘要

研究发现,自闭症谱系障碍(ASD)与几种代谢异常有关,包括线粒体疾病(MD)和异常氧化还原代谢。尽管线粒体功能障碍和氧化应激之间存在密切联系,但 ASD 儿童中 MD 与氧化应激之间的关系尚未得到研究。从符合 Morava 等人标准的可能或确定 MD 的 18 名 ASD 儿童(ASD/MD)和 18 名年龄和性别匹配的无任何生物标志物或 MD 症状的 ASD 儿童(ASD/NoMD)中获得了氧化应激的血浆标志物以及认知和语言发展和 ASD 行为的测量。氧化还原代谢的血浆测量包括还原型游离谷胱甘肽(fGSH)、氧化型谷胱甘肽(GSSG)、fGSH/GSSG 比值和 3-硝基酪氨酸(3NT)。此外,还测量了一种血浆慢性免疫激活标志物 3-氯酪氨酸(3CT)。语言使用学前语言量表或表达性单字词汇测试(取决于年龄)进行测量,适应行为使用 Vineland 适应行为量表(VABS)进行测量,核心自闭症症状使用自闭症症状问卷和社会反应量表进行测量。尽管 ASD/MD 儿童的语言和 ASD 症状相似,但他们的 VABS 沟通和日常生活技能子量表得分较低。与 ASD/NoMD 儿童相比,ASD/MD 儿童的 fGSH/GSSG 比值更高,GSSG 水平更低,表明 ASD/MD 组谷胱甘肽氧化还原状态总体更为有利。然而,与对照组相比,两个 ASD 组的 fGSH 和 fGSH/GSSG 都较低,表明两组都存在氧化还原异常。由于 ASD/MD 组存在年龄相关的影响,因此较年轻的 ASD/MD 儿童的 3CT 水平高于较年轻的 ASD/NoMD 儿童。两组 ASD 儿童的 3CT 水平均明显高于对照组,表明两组 ASD 儿童均存在慢性炎症。有趣的是,3NT 与 ASD/MD 组的认知功能、发育和行为的几个测量值呈正相关,但与 ASD/NoMD 组没有相关性,即较高的 3NT 浓度与更有利的适应行为、语言和 ASD 相关行为相关。为了确定接受药物和/或补充剂的差异是否可以解释 ASD 组之间氧化还原和炎症生物标志物的差异,我们检查了组间药物和补充剂的差异及其对氧化还原和炎症生物标志物的影响。总的来说,ASD/MD 组中接受叶酸、维生素 B12、肉碱、辅酶 Q10、B 族维生素和抗氧化剂的参与者明显更多。然后,我们确定了叶酸、肉碱、辅酶 Q10、B 族维生素和/或抗氧化剂是否会影响氧化还原或炎症生物标志物。抗氧化剂补充剂与 GSSG 显著降低有关,而抗氧化剂、辅酶 Q10 和 B 族维生素与 fGSH/GSSG 比值升高有关。叶酸、肉碱、辅酶 Q10、B 族维生素与 3NT、3CT 或 fGSH 之间没有关系。总的来说,我们的研究结果表明,具有更慢性氧化微环境的 ASD/MD 儿童具有更好的发育。我们根据这样一个事实来解释这一发现,即更活跃的线粒体可以产生更大的氧化微环境,特别是在功能失调时。因此,功能失调的线粒体的代偿性上调可能会以牺牲更氧化的微环境为代价,同时增加活性和功能。尽管更多的 ASD/MD 儿童正在接受某些补充剂,但这些补充剂的使用与与认知发展或行为相关的 ASD/MD 组中的氧化还原生物标志物无关,但可能与两组之间谷胱甘肽代谢的差异有关。这项研究表明,不同亚组的 ASD 儿童有不同的氧化还原异常,这可能来自不同的来源。更好地了解 ASD 中线粒体功能障碍与氧化应激之间的关系,以及可能导致氧化应激的其他因素,对于理解如何指导 ASD 儿童的治疗和管理至关重要。这项研究还表明,识别 ASD/MD 儿童非常重要,因为他们可能会因为特定的代谢特征而对特定的治疗反应不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/337c/3693408/db8e4e288b82/tp201351f1.jpg

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