Complement C1q, Quantitative

CPT: 86160
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Special Instructions

State patient's sex on the request form.


Expected Turnaround Time

7 - 11 days


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Specimen Requirements


Specimen

Serum


Volume

1 mL


Minimum Volume

0.1 mL (Note: This volume does not allow for repeat testing.)


Container

Red-top tube or gel-barrier tube


Collection

Separate serum from cells.


Storage Instructions

Room temperature


Stability Requirements

Temperature

Period

Room temperature

14 days

Refrigerated

14 days

Frozen

14 days

Freeze/thaw cycles

Stable x3


Causes for Rejection

Chylous or lipemic serum; hemolysis; gross bacterial contamination. Plasma should be avoided since fibrin may result in the appearance of nonspecific precipitation, which may adversely affect interpretation.


Test Details


Use

This test is used as an aid in the diagnosis and treatment of systemic lupus erythematosus (SLE).


Methodology

Radial immunodiffusion (RID)


Reference Interval

See table.

Age

Male (mg/dL)

Female (mg/dL)

0 to 1 y

Not established

Not established

2 to 5 y

9.8-18.5

9.7-19.1

6 to 17 y

10.2-19.6

10.2-19.4

>17 y

10.2-20.3

10.3-20.5


Additional Information

Serum levels of C1q are reduced in immune complex disease, SLE and meningitis. An undetectable C1q (a subunit of the first component of complement) in the presence of an absent total complement (CH50) and normal C2, C3 and C4 suggests a congenital deficiency. A low C1q in combination with a low C1 esterase inhibitor and low C4 suggests an acquired C1 esterase inhibitor deficiency.


LOINC® Map

Order Code Order Code Name Order Loinc Result Code Result Code Name UofM Result LOINC
016824 Complement C1q, Quantitative 4478-4 016824 Complement C1q, Quantitative mg/dL 4478-4

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