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Cholinesterase


Also known as: pseudocholinesterase
Formal name: Butyrylcholinesterase; BChE; acylcholine acylhydrolase; EC 3.1.1.8

At a Glance

Why Get Tested?

To find out if you are likely to have temporary paralysis after being given a muscle relaxant called suxamethonium during surgery. This temporary paralysis is called suxamethonium apnoea.

Cholinesterase can also be used to screen for exposure to the effects of organic phosphorus insecticides.

When to Get Tested?

If you or a close relative have experienced suxamethonium apnoea after a surgical operation.

To indicate possible insecticide poisoning with recent or frequent use of organic phosphorus insecticides. Occupational exposure can occur in workers involved with agriculture or the organic chemical industry.

Sample Required?

A blood sample taken from a vein in your arm

Test Preparation Needed?

None.

The Test Sample

What is being tested?

There are two similar cholinesterase enzymes in the body; butyrylcholinesterase (pseudocholinesterase) found in the blood plasma, intestine and white matter, and acetylcholinesterase found in red blood cells, grey matter and nerve endings.

Since butyrylcholinesterase is the enzyme which is involved with the metabolism of the muscle relaxant suxamethonium and affected by exposure to organic phosphorus insecticides, it is this enzyme which is measured in these situations.

The laboratory measures the total activity of cholinesterase in the patient’s blood plasma. This is useful because it indicates whether butyrylcholinesterase levels are low and can quickly find out if the patient is at risk. Low levels can be inherited or acquired as described above.

If the butyrylcholinesterase activity is low the then phenotype studies may be used to help confirm the presence of an unusual (atypical) enzyme, provide more information about any potential risk and assist in family studies.

In order to identify the cholinesterase phenotype the enzyme is incubated with inhibitors such as dibucaine and fluoride. The percentage of the enzyme activity remaining is referred to as a ‘number’ e.g. ‘dibucaine number’, ‘fluoride number’ and is used to assess the phenotype. In this way the laboratory can determine whether the patient has a usual (normal) or an atypical enzyme.

Genetic studies can also be necessary as second-line tests if an atypical variant is difficult for the laboratory to identify or if a silent S gene is suspected. Some laboratories perform these instead of phenotype studies. However in Australia there is currently no Medicare rebate for cholinesterase genetic studies.

How is the sample collected for testing?

A blood sample drawn from a vein in your arm

Is any test preparation needed to ensure the quality of the sample?

No test preparation is needed.

The Test

Common Questions

Ask a Laboratory Scientist

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NOTE: This article is based on research that utilizes the sources cited here as well as the collective experience of the Lab Tests Online Editorial Review Board. This article is periodically reviewed by the Editorial Board and may be updated as a result of the review. Any new sources cited will be added to the list and distinguished from the original sources used.