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Creatine metabolism in patients with urea cycle disorders
- Source :
- Molecular Genetics and Metabolism Reports, Vol 29, Iss, Pp 100791-(2021), Molecular Genetics and Metabolism Reports
- Publication Year :
- 2021
- Publisher :
- Elsevier BV, 2021.
-
Abstract
- The urea cycle generates arginine that is one of the major precursors for creatine biosynthesis. Here we evaluate levels of creatine and guanidinoacetate (the precursor in the synthesis of creatine) in plasma samples (ns = 207) of patients (np = 73) with different types of urea cycle disorders (ornithine transcarbamylase deficiency (ns = 22; np = 7), citrullinemia type 1 (ns = 60; np = 22), argininosuccinic aciduria (ns = 81; np = 31), arginase deficiency (ns = 44; np = 13)). The concentration of plasma guanidinoacetate positively correlated (p<br />Graphical abstract Unlabelled Image
- Subjects :
- Medicine (General)
medicine.medical_specialty
Low protein
UCD, urea cycle disorders
QH301-705.5
Guanidinoacetate methyltransferase deficiency
GAA, guanidinoacetate
ORNT1, ornithine transporter 1
Arginine
Creatine
CT1, creatine transporter 1
chemistry.chemical_compound
R5-920
Endocrinology
AGAT, arginine glycine amidinotransferase
Arginase deficiency
Internal medicine
Genetics
medicine
Creatine deficiency
Biology (General)
NOS, nitric oxide synthase
Molecular Biology
Ornithine transcarbamylase deficiency
Guanidinoacetate
Argininosuccinic acid
Chemistry
medicine.disease
SLC6A8, solute carrier family 6 member 8 gene
ASL, argininosuccinate lyase
Arginase
Urea cycle defect
Argininosuccinic aciduria
Urea cycle
GAMT, guanidino acetate methyltransferase
OTC, ornithine transcarbamylase
ASS, argininosuccinate synthase
Research Paper
Subjects
Details
- ISSN :
- 22144269
- Volume :
- 29
- Database :
- OpenAIRE
- Journal :
- Molecular Genetics and Metabolism Reports
- Accession number :
- edsair.doi.dedup.....d49bc8bafb1f878f5faa68759920ec6a
- Full Text :
- https://doi.org/10.1016/j.ymgmr.2021.100791