1. Creatine metabolism in patients with urea cycle disorders
- Author
-
Nicola Longo, Jean-Leon Chong, Marzia Pasquali, and Filippo Ingoglia
- 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 - 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, Graphical abstract Unlabelled Image
- Published
- 2021
- Full Text
- View/download PDF