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Test ID LBCS Labile Bound Copper, Serum


Ordering Guidance


If CUS1 / Copper, Serum is ordered with this test, it will be canceled, as copper testing will be automatically added as a part of this test order.



Specimen Required


Patient Preparation: High concentrations of gadolinium and iodine are known to potentially interfere with most inductively coupled plasma mass spectrometry-based metal tests. If either gadolinium- or iodine-containing contrast media has been administered, a specimen should not be collected for at least 96 hours.

Supplies:

-Metal Free Specimen Vial (T173)

-Metal Free B-D Tube (No Additive), 6 mL (T184)

Collection Container/Tube: 6-mL Plain, royal blue-top Vacutainer plastic trace element blood collection tube

Submission Container/Tube: 7-mL Metal-free, screw-capped, polypropylene vial

Specimen Volume: 0.75 mL serum

Collection Instructions:

1. For complete instructions, see Metals Analysis Specimen Collection and Transport.

2. Allow the specimen to clot for 30 minutes; then centrifuge the specimen to separate serum from the cellular fraction.

3. Remove the stopper. Carefully pour specimen into metal-free, polypropylene vial, avoiding transfer of the cellular components of blood. Do not insert a pipet into the serum to accomplish transfer, and do not ream the specimen with a wooden stick to assist with serum transfer.

4. Freeze sample on dry ice immediately after pouring off the serum.


Reporting Name

Labile Bound Copper, S

Specimen Type

Serum

Specimen Stability Information

Specimen Type Temperature Time Special Container
Serum Frozen 28 days METAL FREE

Report Available

7 to 15 days

Performing Laboratory

Mayo Clinic Laboratories in Rochester

LOINC Code Information

Test ID Test Order Name Order LOINC Value
LBCS Labile Bound Copper, S 105459-2

 

Result ID Test Result Name Result LOINC Value
620895 Labile Bound Copper, S 96257-1
620896 Labile Bound Copper Fraction 96463-5

Forms

If not ordering electronically, complete, print, and send a Biochemical Genetics Test Request (T798) with the specimen.

Useful For

May be useful in the evaluation of copper-related disorders, including Wilson disease

Day(s) Performed

Wednesday

Test Classification

This test was developed and its performance characteristics determined by Mayo Clinic in a manner consistent with CLIA requirements. It has not been cleared or approved by the US Food and Drug Administration.

CPT Code Information

82525

Specimen Minimum Volume

Serum: 0.5 mL

Reference Values

Labile Bound Copper: <105 ng/mL

 

Labile Bound Copper Fraction:

Males: <10.5 %

Females: <8.1 %

 

Copper, Total:

0-2 months: 40-140 mcg/dL

3-6 months: 40-160 mcg/dL

7-9 months: 40-170 mcg/dL

10-12 months: 80-170 mcg/dL

13 months-10 years: 80-180 mcg/dL

11-17 years: 75-145 mcg/dL

Males:

≥18 years: 73-129 mcg/dL

Females:

≥18 years: 77-206 mcg/dL

Method Name

Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

Additional Tests

Test ID Reporting Name Available Separately Always Performed
CUS1 Copper, S Yes Yes

Testing Algorithm

After a labile-bound copper serum result is obtained, a total copper serum test will be performed at an additional charge. The labile-bound copper concentration will be divided by the total copper concentration to calculate the labile-bound copper fraction result.