Increased amounts of dicarboxylic acids are excreted in human urine under conditions of medium-chain triglyceride (MCT) feeding, abnormal fatty acid oxidation (FAO) and fasting. Criteria to distinguish dicarboxylic aciduria originating from MCT feeding and other conditions are needed in urinary organic acid profiling for detecting inborn errors of metabolism. Patterns of dicarboxylic aciduria in children under various conditions were compared. The relative amounts of medium-chain saturated dicarboxylic acids in urine are not reliable for identifying MCT-induced dicarboxylic aciduria. On the other hand, low ratios of unsaturated to saturated dicarboxylic acids (<0.1) and 3- hydroxydecenedioic to 3-hydroxydecanedioic acids were found to be useful in identifying dicarboxylic aciduria due to MCT ingestion. Additional unique features of dicarboxylic aciduria from MCT are low ratios of 3-hydroxydodecanedioic to 3-hydroxydecanedioic acid (<0.14) and 3-hydroxyadipic to adipic acid (<0.02).

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0026-0495(96)90047-5DOI Listing

Publication Analysis

Top Keywords

dicarboxylic aciduria
16
dicarboxylic acids
12
medium-chain triglyceride
8
feeding abnormal
8
abnormal fatty
8
fatty acid
8
acid oxidation
8
mct feeding
8
saturated dicarboxylic
8
dicarboxylic
6

Similar Publications

Objective: To report a case of glycogen storage disease (GSD) type Ia misdiagnosed as multiple acyl-coenzyme a dehydrogenase deficiency (MADD) by mass spectrometry.

Methods: A 7 months old boy was admitted to our hospital for elevated transaminase levels lasting more than 1 month. His blood biochemistry showed hypoglycemia, metabolic acidosis, hyperlipidemia, elevated lactate and uric acid, elevated alanine amino transferase (ALT), aspartate amino transaminase (AST) and gamma-glutamyl transferase (GGT).

View Article and Find Full Text PDF
Article Synopsis
  • Inborn errors of ketogenesis are rare, serious metabolic disorders that typically cause acute health crises in infants and children due to lipolytic stress, specifically HMGCS and HMGCL deficiencies.* -
  • The study analyzed four patients, their clinical and biochemical data, and utilized advanced genetic testing techniques like whole-exome sequencing to diagnose and understand these conditions, noting that three cases were life-threatening.* -
  • Dietary interventions were implemented, including moderated fat intake and low leucine diets, resulting in no major health issues for the patients in the long-term follow-up, with all living individuals doing well without neurological damage.*
View Article and Find Full Text PDF

Murine deficiency of peroxisomal L-bifunctional protein (EHHADH) causes medium-chain 3-hydroxydicarboxylic aciduria and perturbs hepatic cholesterol homeostasis.

Cell Mol Life Sci

July 2021

Department of Genetics and Genomic Sciences, Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai, 1425 Madison Avenue, Box 1498, New York, NY, 10029, USA.

Peroxisomes play an essential role in the β-oxidation of dicarboxylic acids (DCAs), which are metabolites formed upon ω-oxidation of fatty acids. Genetic evidence linking transporters and enzymes to specific DCA β-oxidation steps is generally lacking. Moreover, the physiological functions of DCA metabolism remain largely unknown.

View Article and Find Full Text PDF

trans-3-Methylglutaconyl CoA isomerization-dependent protein acylation.

Biochem Biophys Res Commun

January 2021

Department of Biochemistry and Molecular Biology, Mail Stop 0330, 1664 N. Virginia Street, University of Nevada, Reno, NV, 89557, USA. Electronic address:

3-methylglutaconic (3MGC) aciduria is associated with a growing number of discrete inborn errors of metabolism. Herein, an antibody-based approach to detection/quantitation of 3MGC acid has been pursued. When trans-3MGC acid conjugated keyhole limpet hemocyanin (KLH) was inoculated into rabbits a strong immune response was elicited.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!