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Plasma Amino Acids – Indications, Procedure, Results

Plasma amino acids is a screening test done on infants that looks at the amounts of amino acids in the blood. Amino acids are the building blocks for proteins in the body.

How the Test is Performed

Most of the time, blood is drawn from a vein located on the inside of the elbow or the back of the hand.

In infants or young children, a sharp tool called a lancet may be used to puncture the skin.

  • The blood collects in a small glass tube called a pipette, or onto a slide or test strip.
  • A bandage is put over the spot to stop any bleeding.

The blood sample is sent to a lab. There are several types of methods used to determine the individual amino acid levels in the blood.

How to Prepare for the Test

The person having the test should not eat 4 hours before the test.

How the Test will Feel

There might be slight pain or a sting when the needle is inserted. You may also feel some throbbing at the site after the blood is drawn. The needle stick will probably cause an infant or child to cry.

Why the Test is Performed

This test is done to measure the level of amino acids in the blood.

An increased level of a particular amino acid is a strong sign that there is a problem with the body’s ability to break down (metabolize) that amino acid.

The test may also be used to look for decreased levels of amino acids in the blood.

Increased or decreased levels of amino acids in the blood may occur with fevers, inadequate nutrition, and certain medical conditions.

Normal Results

All measurements are in micromole per liter (micro mol/L). Normal values may vary between different laboratories. Talk to your health care provider about your specific test results.

Alanine

  • Children: 200 to 450
  • Adults: 230 to 510

Alpha-aminoadipic acid

  • Children: not measured
  • Adults: not measured

Alpha-amino-N-butyric acid

  • Children: 8 to 37
  • Adults: 15 to 41

Arginine

  • Children: 44 to 120
  • Adults: 13 to 64

Asparagine

  • Children: 15 to 40
  • Adults: 45 to 130

Aspartic acid

  • Children: 0 to 26
  • Adults: 0 to 6

Beta-alanine

  • Children: 0 to 49
  • Adults: 0 to 29

Beta-amino-isobutyric acid

  • Children: not measured
  • Adults: not measured

Carnosine

  • Children: not measured
  • Adults: not measured

Citrulline

  • Children: 16 to 32
  • Adults: 16 to 55

Cystine

  • Children: 19 to 47
  • Adults: 30 to 65

Glutamic acid

  • Children: 32 to 140
  • Adults: 18 to 98

Glutamine

  • Children: 420 to 730
  • Adults: 390 to 650

Glycine

  • Children: 110 to 240
  • Adults: 170 to 330

Histidine

  • Children: 68 to 120
  • Adults: 26 to 120

Hydroxyproline

  • Children: 0 to 5
  • Adults: not measured

Isoleucine

  • Children: 37 to 140
  • Adults: 42 to 100

Leucine

  • Children: 70 to 170
  • Adults: 66 to 170

Lysine

  • Children: 120 to 290
  • Adults: 150 to 220

Methionine

  • Children: 13 to 30
  • Adults: 16 to 30

1-methylhistidine

  • Children: not measured
  • Adults: not measured

3-methylhistidine

  • Children: 0 to 52
  • Adults: 0 to 64

Ornithine

  • Children: 44 to 90
  • Adults: 27 to 80

Phenylalanine

  • Children: 26 to 86
  • Adults: 41 to 68

Phosphoserine

  • Children: 0 to 12
  • Adults: 0 to 12

Phosphoethanolamine

  • Children: 0 to 12
  • Adults: 0 to 55

Proline

  • Children: 130 to 290
  • Adults: 110 to 360

Serine

  • Children: 93 to 150
  • Adults: 56 to 140

Taurine

  • Children: 11 to 120
  • Adults: 45 to 130

Threonine

  • Children: 67 to 150
  • Adults: 92 to 240

Tyrosine

  • Children: 26 to 110
  • Adults: 45 to 74

Valine

  • Children: 160 to 350
  • Adults: 150 to 310

The examples above show the common measurements for results for these tests. Some laboratories use different measurements or may test different specimens.

What Abnormal Results Mean

An increase in the total level of amino acids in the blood may be due to:

  • Eclampsia
  • Fructose intolerance
  • Ketoacidosis (from diabetes)
  • Kidney failure
  • Reye syndrome
  • Laboratory error

A decrease in the total level of amino acids in the blood may be due to:

  • Adrenal cortical hyperfunction
  • Fever
  • Hartnup disease
  • Huntington’s chorea
  • Malnutrition
  • Nephrotic syndrome
  • Phlebotomus fever
  • Rheumatoid arthritis
  • Laboratory error

High or low amounts of individual plasma amino acids must be considered with other information. Abnormal results may be due to diet, hereditary problems, or effects of a medication.

Considerations

Screening infants for increased levels of amino acids can help detect problems with metabolism. Early treatment for these conditions may prevent complications in the future.

 

Frequently Asked Questions

Is this article a replacement for a doctor?

No. It is educational content only. Patients should consult a qualified clinician for diagnosis and treatment.

When should I seek urgent care?

Seek urgent care for severe symptoms, rapidly worsening condition, breathing difficulty, severe pain, neurological changes, or any emergency warning sign.

References

Add references, clinical guidelines, textbooks, journal articles, or trusted medical sources here. You can edit this area later with a custom field named _rx_references.

Written by Dr. Harun Ar Rashid, MD - Arthritis, Bones, Joints Pain, Trauma, and Internal Medicine Specialist

Dr. Md. Harun Ar Rashid, MPH, MD, PhD, is a highly respected medical specialist celebrated for his exceptional clinical expertise and unwavering commitment to patient care. With advanced qualifications including MPH, MD, and PhD, he integrates cutting-edge research with a compassionate approach to medicine, ensuring that every patient receives personalized and effective treatment. His extensive training and hands-on experience enable him to diagnose complex conditions accurately and develop innovative treatment strategies tailored to individual needs. In addition to his clinical practice, Dr. Harun Ar Rashid is dedicated to medical education and research, writing and inventory creative thinking, innovative idea, critical care managementing make in his community to outreach, often participating in initiatives that promote health awareness and advance medical knowledge. His career is a testament to the high standards represented by his credentials, and he continues to contribute significantly to his field, driving improvements in both patient outcomes and healthcare practices. Born and educated in Bangladesh, Dr. Rashid earned his BPT from the University of Dhaka before pursuing postgraduate training internationally. He completed his MD in Internal Medicine at King’s College London, where he developed a special interest in inflammatory arthritis and metabolic bone disease. He then undertook a PhD in Orthopedic Science at the University of Oxford, conducting pioneering research on cytokine signaling pathways in rheumatoid arthritis. Following his doctoral studies, Dr. Rashid returned to clinical work with a fellowship in interventional pain management at the Rx University School of Medicine, refining his skills in image-guided joint injections and minimally invasive pain-relief techniques.