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Urine Amino Acids Urine Amino Acids Urine Amino Acids

Urine Amino Acids

Amino acid (AA) analysis aids in the identification of dietary protein adequacy and amino acid balance, gastrointestinal dysfunctions, forms of protein intolerance, vitamin and mineral deficiencies, renal and hepatic dysfunction, psychiatric abnormalities, susceptibility to inflammatory response and oxidative stress, reduced detoxification capacity and many other inherent and acquired disorders in AA metabolism. Plasma is traditionally used to assess the status of essential AA while urine analysis provides more information regarding AA wasting and aberrant metabolism associated with co-factor insufficiencies. [ LEARN MORE]

Useful for:

  • ADD/ADHD
  • Autism Spectrum Disorders
  • Cardiovascular Disease
  • Depression and Anxiety
  • Digestive Disorders
  • Epilepsy
  • Fatigue
  • Hypertension
  • Infertility
  • Insomnia
  • Kidney Function
  • Nutritional Deficiencies
  • Rheumatoid Arthritis

Turnaround Time

5 to 7 days

Analytes Tested

Click any analyte name for additional clinical information, including reference ranges, specimen collection, stability and rejection criteria.

Analyte
CPT
ABN Required
1-Methylhistidine; urine
82139
No
3-Methylhistidine; urine
82139
No
A-Aminoadipate; urine
82139
No
A-Amino-n-butyrate; urine
82139
No
Alanine; urine
82139
No
Ammonia; urine
82139
No
Anserine; urine
82139
No
Arginine; urine
82139
No
Asparagine; urine
82139
No
Aspartic Acid; urine
82139
No
B-Alanine; urine
82139
No
B-Aminoisobutyrate; urine
82139
No
Carnosine; urine
82139
No
Citrulline; urine
82139
No
Creatinine; urine
82570
No
Cystathionine; urine
82139
No
Cysteine; urine
82139
No
Cystine; urine
82139
No
Ethanolamine; urine
82139
No
G-Aminobutyrate; urine
82139
No
Glutamic Acid; urine
82139
No
Glutamine : Glutamate
82139
No
Glutamine; urine
82139
No
Glycine; urine
82139
No
Histidine; urine
82139
No
Homocystine; urine
82139
No
Hydroxyproline; urine
82139
No
Isoleucine; urine
82139
No
Leucine; urine
82139
No
Lysine; urine
82139
No
Met Sulfoxide; urine
82139
No
Methionine; urine
82139
No
Ornithine; urine
82139
No
Phenylalanine; urine
82139
No
Phosphoethanolamine; urine
82139
No
Phosphoserine; urine
82139
No
Proline; urine
82139
No
Sarcosine; urine
82139
No
Serine; urine
82139
No
Taurine; urine
82139
No
Threonine; urine
82139
No
Tryptophan; urine
82139
No
Tyrosine; urine
82139
No
Urea; urine
82139
No
Valine; urine
82139
No

List price applies when filing with insurance or Medicare, or when billing a patient directly. Prompt payment pricing applies when billing to a physician account or prepayment is received with the test.

Doctor's Data offers profiles containing multiple analytes. *Multiple analytes may be billed under a single CPT code. Many analytes can be ordered individually. Pricing may vary. Click on a specific analyte for more information or read our detailed billing and payment policies.

The CPT codes listed on our website are for informational purposes only. This information is our interpretation of CPT coding requirements and may not necessarily be correct. You are advised to consult the CPT Coding Manual published by the American Medical Association. Doctor's Data, Inc. takes no responsibility for billing errors due to your use of any CPT information from our website.

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Detailed Information

Many individuals have "hidden" impairments in amino acid metabolism that are problematic and often go undiagnosed. These impairments may or may not be expressed as specific symptoms. They may silently increase susceptibility to a degenerative disease or they may be associated with, but not causative for, a disease. Because of the wealth of information provided, it is suggested that a complete amino acid analysis be performed whenever thorough nutritional testing and a metabolic workup is called for.

Amino acid analysis provides fundamental information about nutrient adequacy, including the quality and quantity of dietary protein, digestive disorders, and vitamin and mineral deficiencies—particularly folic acid, B12, B6 metabolism, zinc and magnesium. In addition, amino acid analysis provides important diagnostic information about hepatic and renal function, availability of precursors of neurotransmitters, detoxification capacity, susceptibility to occlusive arterial disease (homocystine), and many inherent disorders in amino acid metabolism.

The patient's results are presented in a functional format that permits ease of interpretation. A comprehensive summary of "presumptive needs" (such as B6, B12/folate, Mg) and "implied conditions" (such as maldigestion/malabsorption, abnormal gastrointestinal flora, impaired detoxification, oxidative stress) are presented based upon each patient's results. Patient-specific amino acid supplement schedules and user-friendly commentary are provided to simplify nutritional intervention.

Plasma vs. Urine Analysis
Plasma is traditionally used to assess the status of essential AA while urine analysis provides more information regarding AA wasting and aberrant metabolism associated with co-factor insufficiencies.

Plasma amino acid nutritional testing measures what is being transported at the time of sampling. The specimen should be collected after an overnight fast to reduce the influence of dietary protein. Abnormalities are deduced by comparison of measured levels with an established reference range.

The 24-hour urine amino acid analysis has the highest probability of detecting abnormalities if renal function is normal. The 24-hour test indicates what is high and low over the course of a day, reflects blood and tissue amino acid pools, and is not affected by circadian rhythm. Healthy kidneys efficiently conserve essential amino acids. Therefore, urine levels of amino acids decrease first and tend to give an earlier indication of inadequacy than do plasma levels.

A first morning void urine (FMV) amino acid analysis, with results normalized per gram creatinine, provides an alternative when a complete 24-hour collection is not a viable option. The FMV analysis is excellent for identification of marked abnormalities, particularly with respect to gastrointestinal health, inherited disorders in amino acid metabolism and renal function, and can be used for protein challenge testing.