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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Metabolic profiling of organic acids in urine samples of Cri Du Chat syndrome individuals by gas chromatography-mass spectrometry
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Metabolic profiling of organic acids in urine samples of Cri Du Chat syndrome individuals by gas chromatography-mass spectrometry

机译:通过气相色谱 - 质谱法测定CRI du聊天综合征个体尿液样本中有机酸的代谢分析

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Cri Du Chat (CDC) syndrome is a rare genetic condition caused by the deletion of genetic material on the small arm (the p arm) of chromosome 5. A high-pitched cry that sounds like that of a cat, dysmorphic characteristics, and cytogenetic methods are often used for diagnosing the syndrome. In this study, we applied GC-MS analysis for determining organic acids in urine from 17 control volunteers without CDC syndrome, and from 16 in-dividuals with the CDC syndrome in order to determine the profile of organic acids and biochemical pathways alterations resulting from this genetic condition. First, performing multivariate data analysis selected the best method for extracting organic acids with greater signal intensities and good reproducibility. After selection, multivariate (PLS-DA) and univariate (Mann-Whitney test) data analysis discriminated the metabolites re-sponsible for separation between groups. Nine organic acid metabolites had values of VIP >= 1.0 and p-va-lues <= 0.05, with highest intensities in the samples from CDC individuals, indicating the strongest discriminative power (tricarballylic acid, indoleacetic acid, anthranilic acid, 4-hydroxyphenylacetic acid, 4-hydroxybenzoic acid, 4-hydroxyhippuric acid, pantothenic acid, homovanillic acid, and vanillylmandelic acid). These metabo-lites are involved in several biochemical pathways like in the tyrosine and phenylalanine metabolism, as well as the tryptophan metabolism, which could be associated (i) to some neuropsychiatric alterations commonly ob-served in CDC individuals, (ii) to exogenous compounds related to transformation products by intestinal mi-crobial, and (iii) to a possible deficiency in enzyme activity due to the syndrome.
机译:CRI du聊天(CDC)综合征是一种稀有遗传条件,染色体的小臂(P臂)缺失遗传物质引起的5.一种高音哭泣,听起来像猫,疑难生特征和细胞遗传学的那样方法通常用于诊断综合症。在该研究中,我们应用GC-MS分析来确定从无CDC综合征的17个对照志愿者确定尿液中的有机酸,以及从CDC综合征的16种分类,以确定有机酸和生物化学途径改变的概况遗传条件。首先,进行多变量数据分析选择具有更大信号强度和良好再现性的有机酸提取有机酸的最佳方法。选择后,多变量(PLS-DA)和单变量(MANN-WHITNEY测试)数据分析鉴定了代谢物重新发出的代谢物,以便在组之间分离。九九有机酸代谢物具有VIP> = 1.0和p-Va-Lues <= 0.05的值,具有来自CDC个体的样品中的最高强度,表明最强的辨别力(三碱酸,吲哚乙酸,蒽酸,4-羟基苯基乙酸,4-羟基苯甲酸,4-羟基水平酸,泛酸,同源酸和vanillylmandelic酸)。这些元稀土涉及酪氨酸和苯丙氨酸代谢中的几种生化途径,以及色氨酸代谢,其可以将(i)与一些神经精神改变相关,其在Cdc个体中常见于CDC个体,(ii)到外源化合物与肠道颅颅的转化产物有关,(iii)由于综合征,酶活性的可能缺乏。

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