Literature DB >> 31385327

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

Danielle Zildeana Sousa Furtado1, Fernando Brunale Vilela de Moura Leite1, Leticia Dias Lima Jedlicka1,2, Danilo Santos Souza1,3, Cleber Nunes Barreto1, Heron Dominguez Torres da Silva1, Nilson Antonio Assunção1.   

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.
© 2019 John Wiley & Sons, Ltd.

Entities:  

Keywords:  Cri du Chat Syndrome; metabolism; metabolites; pathways

Year:  2020        PMID: 31385327     DOI: 10.1002/bmc.4673

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  1 in total

1.  Contribution of Congenital Heart Disorders Associated With Copy Number Variants in Mediating Risk for Brain Developmental Disorders: Evidence From 20-Year Retrospective Cohort Study.

Authors:  Luke Dowden; David Tucker; Sian Morgan; Orhan Uzun; Yasir Ahmed Syed
Journal:  Front Cardiovasc Med       Date:  2021-07-15
  1 in total

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