Anticardiolipin Antibodies (ACA), IgG, IgM, Quantitative
Anticardiolipin Antibodies (ACA), IgG, IgM, Quantitative | | | |
| Number | | 161802 |
| CPT | | 86147 (x2) |
Related Information | | Antiphosphatidylserine, IgG,
IgM, IgA
Beta-2 Glycoprotein I
Antibodies, IgG, IgA, IgM |
| Synonyms | | ACA; Antiphospholipids; Cardiolipin Antibodies |
| Test Includes | | IgG and IgM anticardiolipin antibodies |
| Specimen | | Serum |
| Volume | | 1 mL |
| Minimum Volume | | 0.5 mL |
Container | | Red-top tube or gel-barrier tube |
| Storage Instructions | | Refrigerate |
Causes for Rejection | | Hemolysis; lipemia; icteric specimen |
| Reference Interval | | Normal: 0-10 GPL and 0-9 MPL; see also Anticardiolipin Antibodies (ACA), IgA, IgG, IgM. |
Use | | Anticardiolipin antibodies are often present in individuals
with the antiphospholipid antibody syndrome.
1,2 |
Limitations | | ACA can often be observed during the convalescent phase of
acute bacterial and viral infections and in individuals
with syphilis. These infection-induced antibodies are
usually transient and are not associated with an increased
risk of clinical complications. In general, all patients
that test positive for ACA should be retested after six to
eight weeks to rule out transient antibodies that are
usually of no clinical significance. |
Methodology | | Enzyme-linked immunosorbent assay (ELISA) detecting isotype-
specific ACA binding to a microtiter plate coated with
purified cardiolipin antigen. |
Additional Information | | Individuals with the antiphospholipid antibody syndrome
(APS) have an increased risk for stroke, myocardial
infarction, venous thrombosis, thromboembolism,
thrombocytopenia, and/or recurrent miscarriages. In 1999,
an international consensus conference found that one
criterion for the serologic diagnosis of "definite
antiphospholipid syndrome" is the presence of
anticardiolipin antibody of IgG and/or IgM isotype, at
medium or high titer, on two or more occasions, at least
six weeks apart.3 The
presence of ACA of moderate to high
titer for IgG is strongly associated with both arterial and
venous thrombosis and recurrent pregnancy
loss.2,7,8 The IgM
isotype of ACA has also been shown to
be associated with venous thrombosis.
7 Other studies
found that ACA of
the IgA isotype at moderate to high titer can also be
associated with increased risk of APS.
2,12
ACA antibodies are quite common in the general population
and are not always associated with APS. Studies indicate
that there is a higher prevalence of IgM positives than IgG
in the general population with these isotypes occurring in
9.4% and 6.5% of the population, respectively.
4 The
incidence of these ACA is even higher in normal pregnancy
with detection rates of 17% for IgM and 10.6% for IgG.
5
Many of these antibodies are transient and not associated
with APS. The diagnosis of APS should not be made on the
basis of a single ACA result but rather on repeated
positive results obtained at least six weeks apart.
1
The Venereal Disease Research Laboratory (VDRL)
agglutination test that has been used for decades in the
diagnosis of syphilis is based on the detection of
antibodies to cardiolipin.
6 The first solid-phase
immunoassays for ACA were developed in the early
1980's.6 These solid-
phase assays are at least 100 fold
more sensitive than the classical VDRL assay and produce
many more positive results. In general, ACA are considered
to be more sensitive than lupus anticoagulants (LA) for the
detection of APS.7 The
ACA test is positive in 80% to 90%
percent of patients with APS
9 and ACA are implicated
in
approximately five times more cases of APS than are LA.
2
However, LA are considered to be more specific for APS than
ACA.2,9 Due to the
heterogeneity of antibodies
associated with APS, both LA and ACA testing is recommended
when APS is suspected.
7,10
ACA are frequently observed in patients with other
autoimmune disorders and malignancies. Individuals with
ACA secondary to these other conditions are at increased
risk of developing APS. A variety of therapeutic drugs can
induce the production of ACA. These drug-induced
antibodies may be clinically significant if they persist.
2,11 |
Footnotes | | 1. Adcock DM, Jensen R, Johns
CS, Macy PA. Coagulation Handbook. Austin Texas:
Esoterix Coagulation; 2002.
2. Bick RL. Antiphospholipid thrombosis
syndromes. Clin Appl Thromb Hemost. 2001 Oct; 7
(4):241-258.
3. Wilson WA, Gharavi AE, Koike T, et al.
International consensus statement on preliminary
classification criteria for definite antiphospholipid
syndrome: report of an international workshop. Arthritis
Rheum. 1999 Jul; 42(7):1309-1311.
4. Vila P, Hernandez MC, Lopez-Fernandez MF,
Batlle J. Prevalence, follow-up and clinical significance
of the anticardiolipin antibodies in normal subjects.
Thromb Haemost. 1994 Aug; 72(2):209-213.
5. Soloninka CA, Laskin CA, Wither J.
Clinical utility and specificity of anticardiolipin
antibodies. J Rheumatol.
1991 Dec; 18(12):1849-1855.
6. Levine JS, Branch DW, Rauch J. The
antiphospholipid syndrome. N Engl J Med. 2002 Mar 7;
346(10):752-763.
7. Carreras LO, Forastiero RR, Martinuzzo ME.
Which are the best biological markers of the
antiphospholipid syndrome?
J Autoimmun. 2000; 15(2):163-172.
8. Reddel SW, Krilis SA. Testing for and
clinical significance of anticardiolipin antibodies.
Clin Diagn Lab Immunol. 1999; 6(6):775-782.
9. Harris EN, Pierangeli SS, Gharavi AE.
Diagnosis of the antiphospholipid syndrome: a proposal for
use of laboratory tests. Lupus. 1998; 7(Suppl
2):S144-S148.
10. Brandt JT, Triplett DA, Alving B, Scharrer
I. Criteria for the diagnosis of lupus anticoagulants: An
update. On behalf of the Subcommittee on Lupus
Anticoagulant/Antiphospholipid Antibody of the Scientific
and Standardization Committee of the ISTH. Thromb
Haemost. 1995; 74(4):1185-1190.
11. Jenson R. The antiphospholipid antibody
syndrome. Clin Hemost Rev. November 2001; 15(11).
12. Lopez LR, Santos ME, Espinoza LR. Clinical
significance of immunoglobulin A versus immunoglobulins G
and M anticardiolipin antibodies in patients with systemic
lupus erythematosus. Correlation with thrombosis, thrombo-
cytopenia, and recurrent abortion. Am J Clin Pathol.
1992; 98(4):449-454. |
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