Literature DB >> 27940130

Simultaneous measurement of monoamine metabolites and 5-methyltetrahydrofolate in the cerebrospinal fluid of children.

Tomoyuki Akiyama1, Yumiko Hayashi2, Yoshiyuki Hanaoka3, Takashi Shibata3, Mari Akiyama2, Kazuyuki Nakamura4, Yu Tsuyusaki5, Masaya Kubota6, Harumi Yoshinaga3, Katsuhiro Kobayashi3.   

Abstract

BACKGROUND: We describe a new method for simultaneous measurement of monoamine metabolites (3-O-methyldopa [3-OMD], 3-methoxy-4-hydroxyphenylethyleneglycol [MHPG], 5-hydroxyindoleacetic acid [5-HIAA], and homovanillic acid [HVA]) and 5-methyltetrahydrofolate (5-MTHF) and its use on cerebrospinal fluid (CSF) samples from pediatric patients.
METHODS: Monoamine metabolites and 5-MTHF were measured by high-performance liquid chromatography with fluorescence detection. CSF samples were prospectively collected from children according to a standardized collection protocol in which the first 1-ml fraction was used for analysis.
RESULTS: Monoamine metabolites and 5-MTHF were separated within 10min. They showed linearity from the limit of detection to 1024nmol/l. The limit of quantification of each metabolite was sufficiently low for the CSF sample assay. In 42 CSF samples after excluding cases with possibly altered neurotransmitter profiles, the concentrations of 3-OMD, MHPG, 5-HIAA, HVA, and 5-MTHF showed significant age dependence and their ranges were comparable with the reference values in the literature. The metabolite profiles of aromatic l-amino acid decarboxylase deficiency, Segawa disease, and folate receptor α defect by this method were compatible with those in the literature.
CONCLUSIONS: This method is a simple means of measuring CSF monoamine metabolites and 5-MTHF, and is especially useful for laboratories not equipped with electrochemical detectors.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  3-O-methyldopa; 3-methoxy-4-hydroxyphenylethyleneglycol; 5-hydroxyindoleacetic acid; 5-methyltetrahydrofolate; Aromatic l-amino acid decarboxylase deficiency; Cerebral folate deficiency; Folate receptor α defect; Homovanillic acid; Neurotransmitters

Mesh:

Substances:

Year:  2016        PMID: 27940130     DOI: 10.1016/j.cca.2016.12.005

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN: 0009-8981            Impact factor:   3.786


  3 in total

1.  Analysis of human cerebrospinal fluid monoamines and their cofactors by HPLC.

Authors:  Marta Batllori; Marta Molero-Luis; Aida Ormazabal; Mercedes Casado; Cristina Sierra; Angels García-Cazorla; Manju Kurian; Simon Pope; Simon J Heales; Rafael Artuch
Journal:  Nat Protoc       Date:  2017-10-19       Impact factor: 13.491

2.  Impact of Nitisinone on the Cerebrospinal Fluid Metabolome of a Murine Model of Alkaptonuria.

Authors:  Andrew S Davison; Brendan P Norman; Hazel Sutherland; Anna M Milan; James A Gallagher; Jonathan C Jarvis; Lakshminarayan R Ranganath
Journal:  Metabolites       Date:  2022-05-25

3.  Hereditary folate malabsorption due to a mutation in the external gate of the proton-coupled folate transporter SLC46A1.

Authors:  Srinivas Aluri; Rongbao Zhao; Charlotte Lubout; Susanna M I Goorden; Andras Fiser; I David Goldman
Journal:  Blood Adv       Date:  2018-01-05
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.