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Test ID ACHS Acetylcholinesterase, Erythrocytes

Useful For

Detecting effects of remote (months) past exposure to cholinesterase inhibitors (organophosphate insecticide poisoning)

Method Name

Spectrophotometric-Thiocholine Production

Reporting Name

Acetylcholinesterase, RBC

Specimen Type

Whole Blood EDTA

Specimen must arrive within 72 hours of draw.

 

Container/Tube: Lavender top (EDTA)

Specimen Volume: 4 mL

Additional Information: Date of draw is required.

Specimen Minimum Volume

2.5 mL

Specimen Stability Information

Specimen Type Temperature Time
Whole Blood EDTA Refrigerated

Clinical Information

Acetylcholinesterase (AChE) is anchored to the external surface of the RBC. Its appearance in a lysate of red cells is diminished in paroxysmal nocturnal hemoglobinuria (PNH). The use of red cell AChE for PNH has not gained widespread acceptance, and flow cytometry testing is most often used for PNH (see PANH/81156 PI-Linked Antigen, Blood).

 

Red cell AChE is most often used to detect past exposure to organophosphate insecticides with resultant inhibition of the enzyme. Both the pseudocholinesterase activity in serum and red cell AChE are inhibited by these insecticides, but they are dramatically different vis-a-vis the temporal aspect of the exposure. The half-life of the pseudo-enzyme in serum is about 8 days, and the "true" cholinesterase (AChE) of red cells is over 3 months (determined by erythropoietic activity). Recent exposure up to several weeks is determined by assay of the pseudo-enzyme and months after exposure by measurement of the red cell enzyme. The effect of the specific insecticides may be important to know prior to testing.

Reference Values

31.2-61.3 U/g of hemoglobin

Cautions

Make sure the potential offending agent is, indeed, an acetylcholinesterase inhibitor.

 

Pseudocholinesterase acitivity in serum is the appropriate test for succinylcholine sensitivity to anesthesia.

Day(s) Performed

Tuesday, Friday; 10 a.m.

Report Available

4 days

Performing Laboratory

Mayo Medical Laboratories in Rochester

Test Classification

This test has been cleared or approved by the U.S. Food and Drug Administration and is used per manufacturer's instructions. Performance characteristics were verified by Mayo Clinic in a manner consistent with CLIA requirements.

CPT Code Information

82482

NY State Approved

Yes