Literature DB >> 831385

Low molecular weight organic acids in the urine of the newborn.

N Gregersen, J Ingerslev, K Rasmussen.   

Abstract

The urinary excretion of seven selected low molecular weight organic acids in normal neonates was measured by gas chromatography. First and third to fourth day of life excretion of the following compounds was significantly unchanged: 3-OH-butyric acid (less than 13 mumol/mmol creatinine), succinic acid (approx. 43 mumol/mmol creatinine), adipic acid (approx. 12 mumol/mmol creatinine), 2-OH-glutaric acid (approx. 23 mumol/mmol creatinine), 3-OH-3-Me-glutaric acid (approx. 25 mumol/mmol creatinine) and citric acid (approx. 115 mumol/mmol creatinine). The excretion of 4-OH-phenyl-acetic acid increased during the first four days of life (from less than 8 mumol/mmol creatinine to approx. 20 mumol/mmol creatinine). It is postulated that urinary orgainc acid excretion in the neonate, which is clearly different from the adult urinary pattern, is a reflection of the specific neonatal metabolic situation, including a high fatty acid utilisation and a low protein catabolism.

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Year:  1977        PMID: 831385     DOI: 10.1111/j.1651-2227.1977.tb07812.x

Source DB:  PubMed          Journal:  Acta Paediatr Scand        ISSN: 0001-656X


  12 in total

1.  Generalised dicarboxylic aciduria: a common finding in neonates.

Authors:  M Downing; P Rose; M J Bennett; N J Manning; R J Pollitt
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

Review 2.  D-2-Hydroxyglutaric aciduria: unravelling the biochemical pathway and the genetic defect.

Authors:  Eduard A Struys
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

3.  Saccharomyces cerevisiae Forms D-2-Hydroxyglutarate and Couples Its Degradation to D-Lactate Formation via a Cytosolic Transhydrogenase.

Authors:  Julia Becker-Kettern; Nicole Paczia; Jean-François Conrotte; Daniel P Kay; Cédric Guignard; Paul P Jung; Carole L Linster
Journal:  J Biol Chem       Date:  2016-01-16       Impact factor: 5.157

4.  Biochemical studies in a patient with defects in the metabolism of acyl-CoA and sarcosine: another possible case of glutaric aciduria type II.

Authors:  N Gregersen; S Kølvraa; K Rasmussen; E Christensen; N J Brandt; F Ebbesen; F H Hansen
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

Review 5.  Progress in understanding 2-hydroxyglutaric acidurias.

Authors:  Martijn Kranendijk; Eduard A Struys; Gajja S Salomons; Marjo S Van der Knaap; Cornelis Jakobs
Journal:  J Inherit Metab Dis       Date:  2012-03-06       Impact factor: 4.982

6.  An interesting case of metabolic dystonia: L-2 hydroxyglutaric aciduria.

Authors:  Padma Balaji; V Viswanathan; Amarnath Chellathurai; Debasis Panigrahi
Journal:  Ann Indian Acad Neurol       Date:  2014-01       Impact factor: 1.383

7.  Exploring the Role of Different Neonatal Nutrition Regimens during the First Week of Life by Urinary GC-MS Metabolomics.

Authors:  Angelica Dessì; Antonio Murgia; Rocco Agostino; Maria Grazia Pattumelli; Andrea Schirru; Paola Scano; Vassilios Fanos; Pierluigi Caboni
Journal:  Int J Mol Sci       Date:  2016-02-22       Impact factor: 5.923

8.  Evidence that 2-hydroxyglutarate is not readily metabolized in colorectal carcinoma cells.

Authors:  Susan J Gelman; Nathaniel G Mahieu; Kevin Cho; Elizabeth M Llufrio; Timothy A Wencewicz; Gary J Patti
Journal:  Cancer Metab       Date:  2015-12-01

9.  The Urinary Metabolome of Healthy Newborns.

Authors:  Yamilé López-Hernández; Juan José Oropeza-Valdez; Jorge O Blanco-Sandate; Ana Sofia Herrera-Van Oostdam; Jiamin Zheng; An Chi Guo; Victoria Lima-Rogel; Rahmatollah Rajabzadeh; Mariana Salgado-Bustamante; Jesus Adrian-Lopez; C G Castillo; Emilia Robles Arguelles; Joel Monárrez-Espino; Rupasri Mandal; David S Wishart
Journal:  Metabolites       Date:  2020-04-23

Review 10.  Metabolism, Activity, and Targeting of D- and L-2-Hydroxyglutarates.

Authors:  Dan Ye; Kun-Liang Guan; Yue Xiong
Journal:  Trends Cancer       Date:  2018-01-05
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