Phophoethanolamine, a nonessential phosphorous bearing amino acid, is low in this urine specimen.
Phosphoethanolamine is derived from dietary sources and is also formed endogenously from serine via phosphorylation of ethanolamine.
When ethanolamine is high or normal and phosphoethanolamine is low there is a presumptive need for magnesium (magnesium dependent kinase). Phosphoethanolamine is a precursor of phosphotidyl choline, choline and the neurotransmitter acetylcholine. If low phosphoethanolamine results in low acetylcholine, and there is insufficient choline from dietary lecithin, there may be depressed activity of the parasympathetic nervous system (eg. decreased peristalsis, ability to sweat), and poor memory and cognitive function. Low phosphoethanolamine is usually the result of magnesium deficiency or protein malnutrition.
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1-Methylhistidine, 3-Methylhistidine, Alanine, Alpha-amino-N-butyrate, Alpha-aminoadipate, Ammonia (NH4), Ammonia Level (NH4), Anserine, Arginine, Asparagine, Aspartate, Beta-alanine, Beta-aminoisobutyrate, Carnosine, Citrulline, Creatinine, Cystathionine, Cysteine, Cystine, Ethanolamine, Gamma-aminobutyrate, Glutamate, Glutamine, Glutamine/Glutamate, Glycine, Histidine, Homocystine, Hydroxyproline, Isoleucine, Leucine, Lysine, Methionine, Methionine Sulfoxide, Ornithine, Phenylalanine, Phosphoethanolamine, Phosphoserine, Proline, Sarcosine, Serine, Taurine, Threonine, Tryptophan, Tyrosine, Urea, Valine
