Literature DB >> 18722797

Technical and biochemical factors affecting cerebrospinal fluid 5-MTHF, biopterin and neopterin concentrations.

M M Verbeek1, A M Blom, R A Wevers, A J Lagerwerf, J van de Geer, M A A P Willemsen.   

Abstract

BACKGROUND: The diagnosis of pediatric neurologic disorders with a deficiency in the biosynthesis of either the neurotransmitters serotonin and dopamine, or the co-factor tetrahydrobiopterin or a cerebral 5-methyltetrahydrofolate (5-MTHF) deficiency, strongly relies on a robust analysis of neurotransmitter metabolites, pterins and 5-MTHF in the cerebrospinal fluid (CSF). The aim of this study was to investigate which technical and biochemical factors affect the CSF concentration of 5-MTHF, neopterin and biopterin in a pediatric population.
METHODS: We studied effects of the ventriculo-spinal gradient, total protein concentration, pretreatment with ascorbic acid (in case of 5-MTHF analysis), pretreatment of CSF with trichloro acetic acid (TCA)/dithiotreitol (DTE) and oxidation with either iodine or manganese oxide (in case of pterin analysis), storage time and age of the patients. We included CSF samples from children until the age of 18 years and analysed 5-MTHF, neopterin, biopterin, homovanillic acid (HVA), 5-hydroxy-indoleacetic acid (5-HIAA) and total protein.
RESULTS: The major findings of our study are: (1) CSF 5-MTHF, neopterin and biopterin concentrations are not affected by the ventriculo-spinal gradient; (2) pretreatment of CSF with ascorbic acid has negligible effects on 5-MTHF concentrations; (3) pretreatment of CSF with TCA/DTE and oxidation with iodine results in the most accurate determination of neopterin and biopterin; (4) when adjusted for age and total protein, CSF 5-MTHF correlated with 5-HIAA, but not with HVA; (5) the reference value of 5-MTHF in CSF in childhood is age-dependent (r=-0.634; p0.001); (6) we did not observe an age-dependency for neopterin and biopterin in CSF.
CONCLUSION: 5-MTHF, neopterin and biopterin can be analysed in any volume of CSF that is collected. For correct analysis of pterins, CSF will have to be pretreated to stabilize the concentrations and stored properly, whereas such pretreatment is not necessary for 5-MTHF.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18722797     DOI: 10.1016/j.ymgme.2008.07.004

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  12 in total

1.  Simultaneous determination of all forms of biopterin and neopterin in cerebrospinal fluid.

Authors:  Pierre Guibal; Nathalie Lévêque; Diane Doummar; Nicolas Giraud; Emmanuel Roze; Diana Rodriguez; Rémy Couderc; Thierry Billette De Villemeur; Fathi Moussa
Journal:  ACS Chem Neurosci       Date:  2014-04-08       Impact factor: 4.418

Review 2.  Mechanisms of membrane transport of folates into cells and across epithelia.

Authors:  Rongbao Zhao; Ndeye Diop-Bove; Michele Visentin; I David Goldman
Journal:  Annu Rev Nutr       Date:  2011-08-21       Impact factor: 11.848

Review 3.  The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption.

Authors:  Rongbao Zhao; Srinivas Aluri; I David Goldman
Journal:  Mol Aspects Med       Date:  2016-09-21

4.  Sulfa drugs inhibit sepiapterin reduction and chemical redox cycling by sepiapterin reductase.

Authors:  Shaojun Yang; Yi-Hua Jan; Vladimir Mishin; Jason R Richardson; Muhammad M Hossain; Ned D Heindel; Diane E Heck; Debra L Laskin; Jeffrey D Laskin
Journal:  J Pharmacol Exp Ther       Date:  2014-12-30       Impact factor: 4.030

5.  Identification of novel mutations in the proton-coupled folate transporter (PCFT-SLC46A1) associated with hereditary folate malabsorption.

Authors:  Daniel Sanghoon Shin; Kris Mahadeo; Sang Hee Min; Ndeye Diop-Bove; Peter Clayton; Rongbao Zhao; I David Goldman
Journal:  Mol Genet Metab       Date:  2011-01-25       Impact factor: 4.797

6.  Functional roles of aspartate residues of the proton-coupled folate transporter (PCFT-SLC46A1); a D156Y mutation causing hereditary folate malabsorption.

Authors:  Daniel Sanghoon Shin; Sang Hee Min; Laura Russell; Rongbao Zhao; Andras Fiser; I David Goldman
Journal:  Blood       Date:  2010-08-30       Impact factor: 22.113

7.  Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism.

Authors:  Robert Steinfeld; Marcel Grapp; Ralph Kraetzner; Steffi Dreha-Kulaczewski; Gunther Helms; Peter Dechent; Ron Wevers; Salvatore Grosso; Jutta Gärtner
Journal:  Am J Hum Genet       Date:  2009-09       Impact factor: 11.025

8.  A novel deletion mutation in the proton-coupled folate transporter (PCFT; SLC46A1) in a Nicaraguan child with hereditary folate malabsorption.

Authors:  N Diop-Bove; M Jain; F Scaglia; I D Goldman
Journal:  Gene       Date:  2013-06-28       Impact factor: 3.688

9.  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

10.  Single-Step Rapid Diagnosis of Dopamine and Serotonin Metabolism Disorders.

Authors:  Aurélien Lo; Pierre Guibal; Diane Doummar; Diana Rodriguez; Jean-Yves Hautem; Rémy Couderc; Thierry Billette De Villemeur; Emmanuel Roze; Pierre Chaminade; Fathi Moussa
Journal:  ACS Omega       Date:  2017-09-19
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.