Lab Test

Anti Cardiolipin Antibodies (IgG, IgM)

Anti-Cardiolipin Antibodies, ACL-IgG, ACL-IgM, ACL-IgA, Cardiolipin Antibodies, IgG, IgM, IgA

Test Codes

EPIC: LAB5166, Beaker: ACL, Antrim #30954

Department

Special Chemistry

Specimen Collection Criteria

Collect: One Gold-top SST tube. (Minimum Whole Blood 2.0 mL)

Physician Office/Draw Specimen Preparation

Let specimen clot 30-60 minutes then immediately centrifuge to separate serum from cells. Refrigerate (2-8°C or 36-46°F) the centrifuged collection tube within two hours of collection. (Minimum Serum: 0.5 mL)

Preparation for Courier Transport

Transport: Centrifuged collection tube, refrigerated (2-8°C or 36-46°F). (Minimum Serum: 0.5 mL)

Rejection Criteria

  • Plasma specimens.
  • Severely hemolyzed, lipemic or icteric specimens.   

In-Lab Processing

Let specimen clot 30-60 minutes then immediately centrifuge to separate serum from cells. Room temperature is acceptable for a maximum of two hours. (Minimum Serum: 0.5 mL)


Storage

Specimen Stability for Testing:

Centrifuged SST Tubes and Microtainers® with Separator Gel
Room Temperature (20-26°C or 68-78.8°F): 2 hours
Refrigerated (2-8°C or 36-46°F): 7 days
Frozen (-20°C/-4°F or below): Unacceptable

Red-top Tubes and Microtainers® without Separator Gel
Room Temperature (20-26°C or 68-78.8°F): 2 hours
Refrigerated (2-8°C or 36-46°F): 7 days
Frozen (-20°C/-4°F or below): Unacceptable

Serum Specimens (Pour-Overs)
Room Temperature (20-26°C or 68-78.8°F): 2 hours
Refrigerated (2-8°C or 36-46°F): 7 days
Frozen (-20°C/-4°F or below): 7 days

Specimen Storage in Department Prior to Disposal:

Refrigerated (2-8°C or 36-46°F): 7 days

Laboratory

Royal Oak Special Testing Laboratory

Performed

Monday, Wednesday, Friday.
Results available within 2 business days.

Reference Range

 Cardiolipin IgG (GPL-U/mL)Cardiolipin IgM (MPL-U/mL)
Negative< 20< 20
EquivocalNANA
Positive≥ 20≥ 20

Test Methodology

Multiplex Flow Assay.

Interpretation

Elevated cardiolipin antibodies (aCL) are seen in antiphospholipid syndrome (APS), greater than 20% of patients with SLE, 40-46% of rheumatoid arthritis patients, 50% of AIDS patients, patients with viral, bacterial, protozoan infections and malignancies (e.g., hairy cell leukemia, malignant lymphoma, and Waldenstrom's macrglobulinemia). Medications including quinidine, procainamide, chlorpromazine, phenytoin, and many antibiotics have been associated with increased aCL levels.

According to the most recent international consensus statement (see reference), the Antiphospholipid syndrome (APS) is present if at least one clinical criterion and one laboratory criterion are present.

Clinical criteria include:

  1. Vascular thrombosis (arterial, venous, small vessel).
  2. Pregnancy morbidities with fetal loss.

Laboratory criteria: these must occur on 2 or more occasions, at least 12 weeks apart and include:

  1. Anticardiolipin antibodies positive with IgG greater than 40 GPL and/or IgM greater than 40 MPL. (NOTE: IgA anticardiolipin antibodies are not currently considered to be a laboratory criterion.)
  2. Anti-beta 2 glycoprotein I antibodies positive with IgG greater than 20 GPL and/or IgM greater than 10 MPL.
  3. Lupus anticoagulant detected in plasma.

A diagnosis of APS is discouraged if less than 12 weeks or more than 5 years separates the positive laboratory and clinical criteria.

NOTE: Anticardiolipin antibodies may occur following acute bacterial or viral infections and in syphilis. Patients with such a history, who test positive, should be retested in 6-8 weeks to exclude transient antibodies that are usually not clinically significant.

Clinical Utility

To aid in the diagnosis of antiphospholipid syndrome.

Reference

  1. J. Thrombosis and Haemostasis 2006; 4:295-306.

CPT Codes

86147 x 3.
LOINC: 3182-3, 3181-5, 8063-0

Contacts

Last Updated

2/10/2024

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