Journal of Inherited Metabolic Disease · 2000 · 21 citations · 6 references
MedicineNephrologyRenal PathophysiologyEnzyme DeficienciesRenal DiseaseRenal Function TestsRenal ImpairmentBlood Urea Nitrogen To Creatinine RatioCreatine Metabolism DisordersCreatinine Analysis In Body FluidsCreatinine Clearance MonitoringCreatinine-based BiomarkersSerum Creatine Kinase AssessmentSerum Creatinine Assessment
Guanidinoacetate methyltransferase (GAMT) deficiency (creatine deficiency syndrome) is a recently discovered inborn error of creatine biosynthesis. Affected patients have elevated concentrations of guanidino-acetate, the metabolic precursor of creatine, in urine, plasma and cerebrospinal fluid. In addition, urinary creatinine excretion and plasma creatinine concentration are decreased. For biochemical evaluation of patients suspected to suffer from GAMT deficiency, correct quantification of creatinine in plasma is important. Here we report our experience with different quantification techniques. We found that creatinine in plasma from two GAMT-deficient patients appeared normal when measured by the Jaffé method but was decreased when measured enzymatically or by HPLC. The apparently normal levels of creatinine as measured by the Jaffé method were not caused by guanidinoacetate. In urine, the Jaffé method and the enzymatic method gave similar results, indicating that in urine no false elevations of creatinine can be expected. As the Jaffé method is still widely used for routine plasma creatinine measurements, it is important to realize it cannot be used to exclude GAMT deficiency.
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Guanidinoacetate methyltransferase deficiency: New clinical features
Vijeya Ganesan, Andrew Johnson, Alan Connelly et al. · Pediatric Neurology · 1997 · 108 citations
Eduard A. Struys, Erwin E. W. Jansen, H.J. ten Brink et al. · Journal of Pharmaceutical and Biomedical Analysis · 1998 · 81 citations