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Prolidase, Serum or Plasma

Published: August 9, 2026Updated: August 16, 2026

This test measures the amount of the enzyme prolidase in a sample of serum or plasma, usually to help evaluate a rare inherited condition called prolidase deficiency.

Quick summary

["Prolidase testing helps detect a rare enzyme deficiency that can cause skin ulcers, recurrent infections, and other health problems."]

Medically reviewed by WellAlly Editorial TeamLast reviewed August 16, 2026Editorial policy

Key facts at a glance

LOINC
47735-6
Short code
Proline SFr SerPl
Synonyms
Proline SFr SerPl
Category
chemistry
Sample
serum
Container
Red-top tube (SST)
Units
N/A
Fasting
false
Population
adult
Sex
all
Age range
18–65 years
Specimen volume
5 mL
Stability
Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
Hemolysis max
500
Lipemia max
1000
Icterus max
500
TAT
4–24 hours
Order
routine

What Is Prolidase?

Prolidase is an enzyme that helps break down certain protein building blocks, particularly dipeptides that contain the amino acid proline. This enzyme is important for normal recycling of collagen and for many cellular processes. It is found in tissues throughout the body and small amounts can be measured in blood.

Why This Test Is Ordered

Doctors may order a prolidase level when a person has signs that could suggest prolidase deficiency, a rare inherited disorder. Features can include long-lasting skin ulcers, frequent infections, distinctive facial features, and developmental problems. Testing may also be used to help confirm a suspected diagnosis or to monitor someone known to have the condition.

How the Test Is Performed

This test uses a blood sample, typically drawn from a vein in your arm. The sample is collected into a tube and then sent to a laboratory that measures enzyme activity in serum or plasma. In some cases, testing may also be done on other samples, such as skin cells, but the serum or plasma test is one way to look at prolidase.

What the Results Mean

A low prolidase level can support a diagnosis of prolidase deficiency, while a normal level generally makes that diagnosis less likely. Results are interpreted together with symptoms, family history, and other tests, and sometimes genetic testing is needed to confirm the diagnosis. Because this is a specialized test, your care team will explain what your specific result means for you.

Clinical interpretation

How abnormal results are interpreted and what conditions they suggest.

◆Associated findings1

Short name

Prolidase

Frequently asked questions

Is prolidase deficiency common?
No. Prolidase deficiency is a very rare inherited condition, so this test is usually only ordered when a person has specific symptoms or a family history that raises suspicion.
Do I need to fast before a prolidase blood test?
Fasting is generally not required for this test, but follow any instructions your healthcare provider or laboratory gives you, since preparation can depend on the specific lab method being used.
Can a low prolidase result confirm the diagnosis on its own?
Not usually. A low result can support the diagnosis, but doctors typically combine it with symptoms, family history, and often genetic testing to confirm prolidase deficiency.
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy