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靶向分析揭示了5号染色体短臂缺失个体中通路的改变。

Targeted analysis reveals alteration in pathway in 5p minus individuals.

作者信息

Furtado Danielle Zildeana Sousa, Leite Fernando Brunale Vilela de Moura, Jedlicka Leticia Dias Lima, Souza Danilo Santos, Barreto Cleber Nunes, da Silva Heron Dominguez Torres, Assunção Nilson Antonio

机构信息

Laboratório de Radicais Livres em Sistemas Biológicos e Bioanalítica, Instituto de Ciências Ambientais, Químicas e Farmacêuticas, Universidade Federal de São Paulo, Brazil.

Instituto de Estudos em Saúde e Biológicas, Saúde Coletiva, Universidade Federal do Sul e Sudeste do Pará, Brazil.

出版信息

Biomed Chromatogr. 2020 Jan;34(1):e4673. doi: 10.1002/bmc.4673. Epub 2020 Jan 2.

Abstract

Cri du Chat or 5p minus (5p-) syndrome is characterized by a deletion located on the chromosome 5 short (-p) arm and has an incidence rate of 1 in 50,000 individuals worldwide. This disease manifests in disturbances across a range of systems biochemicals. Therefore, a targeted metabolomics analysis was evaluated in patients with 5p- syndrome to help unravel the biochemical changes that occur in this disease. Urine samples were collected from people of both sexes aged 1-38 years old and analyzed by ultra-performance liquid chromatography coupled to mass spectrometry. Student' statistical test, metabolomic pathway analysis and metabolite set enrichment analysis were applied to the data. Alterations of some amino acids and amine biogenics levels were found in Cri du Chat Syndrome individuals. The alteration of most of these metabolites is associated with energy recuperation and glycolysis. In general, we found the catabolism of some metabolic pathways to be affected in 5p- patients.

摘要

猫叫综合征或5号染色体短臂缺失(5p-)综合征的特征是5号染色体短(-p)臂上存在缺失,全球发病率为五万分之一。这种疾病表现为一系列系统生化过程的紊乱。因此,对5p-综合征患者进行了靶向代谢组学分析,以帮助揭示该疾病中发生的生化变化。收集了年龄在1至38岁的男女尿液样本,并通过超高效液相色谱-质谱联用进行分析。将学生统计检验、代谢组学通路分析和代谢物集富集分析应用于数据。在猫叫综合征个体中发现了一些氨基酸和胺类生物合成水平的改变。这些代谢物中的大多数改变与能量恢复和糖酵解有关。总体而言,我们发现5p-患者的一些代谢途径分解代谢受到影响。

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