Skip to content
PubMed This is a summary of 12 peer-reviewed journal articles Updated
Antiphospholipid Syndrome

How Do I Interpret Antiphospholipid IgG and IgM Levels?

At a Glance

A positive or high antiphospholipid antibody result does not by itself diagnose antiphospholipid syndrome (APS). Doctors consider the antibody type and level, whether it remains positive at least 12 weeks later, and whether you have had a documented blood clot or specific pregnancy complication.

Antiphospholipid antibody lab reports can be overwhelming, full of acronyms and numbers. Interpreting them requires understanding which specific tests were run, the amount of antibody found, and whether the results remain positive over time. Most importantly, having positive antibodies on a lab report does not automatically mean you have Antiphospholipid Syndrome (APS). Doctors use medical classification criteria as a framework, which look for both a qualifying clinical event and persistent laboratory evidence [1].

The Three Core APS Tests

A comprehensive APS laboratory evaluation typically involves three main tests. The first two count the amount of antibodies in your blood, while the third tests how your blood functions:

  • Anticardiolipin (aCL) and Anti-β2-glycoprotein I (anti-β2GPI): These tests use laboratory methods (like ELISA) to detect specific antibodies in your blood serum [2]. They are reported by their type (IgG or IgM) and their concentration.
  • Lupus Anticoagulant (LA): Despite its name, this is not a test for lupus. Rather than counting antibodies, it is a functional test that measures how long it takes your blood to clot in a test tube (often appearing on reports as “dRVVT” or aPTT) [3]. LA results are usually reported as positive or negative, rather than as an IgG or IgM level.

Interpreting Antibody Risk Profiles

For aCL and anti-β2GPI, laboratories test for two classes of antibodies: IgG and IgM [2].
While both can be important, your overall clinical risk is not determined by a single test. Instead, doctors look at your complete antibody profile. Being “triple positive” (testing persistently positive for LA, aCL, and anti-β2GPI) is associated with the highest clinical risk [4]. Isolated or low-level results generally carry a lower risk, but your personal risk also depends heavily on your medical history, such as prior blood clots or other health conditions [4].

Understanding Titers, Units, and Thresholds

The “titer” refers to the concentration of aCL or anti-β2GPI antibodies detected.

  • Units: Anticardiolipin is often reported in GPL (for IgG) or MPL (for IgM) units [5]. Anti-β2GPI tests use different, assay-specific units [6].
  • Thresholds and the 99th Percentile: Different medical guidelines use specific cutoffs for research and classification. The traditional guidelines (often called the Sydney criteria) consider an aCL result positive if it is greater than 40 GPL/MPL or above the 99th percentile of a healthy population [7]. Newer 2023 classification criteria (for specific testing methods) categorize 40 to 79 units as “medium” and 80 or above as “high” [7] [6].

Because laboratories use different chemical kits and equipment, a “40” in one lab might not mean the same thing as a “40” in another [8]. There is no universal standard, so you must always interpret your numbers using the specific reference range provided on your individual lab report [5] [8].

The 12-Week Rule: Assessing Persistence

A single positive test result does not confirm persistent antibodies. Antiphospholipid antibodies can be temporary, sometimes spiking during acute infections (like viruses) or periods of inflammation [9].

Because temporary spikes happen, medical guidelines require repeating the tests at least 12 weeks later [1]. If the second test is negative, it means the required persistence has not been demonstrated.

Important Safety Note: Blood thinners (anticoagulants like warfarin, heparin, or DOACs) can severely interfere with Lupus Anticoagulant (LA) testing, causing false-positive or false-negative results [10]. Never stop or alter your anticoagulant medication for a blood test without explicit instructions from your prescribing doctor.

Antibodies vs. Clinical Guidelines

Having high or persistent antibodies means you carry them, but an APS diagnosis also requires a qualifying clinical event [1]. In standard classification guidelines, these events include:

  • An objectively confirmed blood clot (venous, arterial, or small-vessel) [11].
  • Specific pregnancy complications, such as one or more unexplained fetal deaths at or beyond 10 weeks, premature birth before 34 weeks due to severe preeclampsia or placental insufficiency, or three or more consecutive unexplained miscarriages before 10 weeks [12].

These criteria help standardize research, but real-life diagnosis relies on a specialist’s judgment of your entire health history. Do not start, stop, or change aspirin, blood thinners, or other medications based solely on a lab number; always consult your doctor to discuss what your specific results mean for you.

Common questions in this guide

What do IgG and IgM mean on an antiphospholipid antibody report?
IgG and IgM are two classes of antibodies measured in anticardiolipin and anti-β2-glycoprotein I testing. The report may list the amount of each class, but one result should not be interpreted alone; clinicians consider your complete antibody profile and medical history.
How should I understand the titer or number on my report?
A titer is the amount of anticardiolipin or anti-β2-glycoprotein I antibody detected. Results may use GPL or MPL units, or assay-specific units, and laboratories use different methods, so compare the number with the reference range from that laboratory rather than another report.
Does a high or positive antiphospholipid antibody result mean I have APS?
No. APS is not diagnosed from a single high or positive antibody result; clinicians look for persistent laboratory positivity and a qualifying clinical event, such as an objectively confirmed blood clot or certain pregnancy complications. Your clinician must interpret the result with your medical history.
Why do I need repeat antiphospholipid testing after 12 weeks?
Antiphospholipid antibodies can temporarily increase during an infection or other inflammation. Testing again at least 12 weeks later shows whether the antibody remains positive; if the repeat result is negative, the required persistence has not been demonstrated.
Can blood thinners affect my lupus anticoagulant test?
Yes. Warfarin, heparin, and direct oral anticoagulants can interfere with lupus anticoagulant testing and may cause a false-positive or false-negative result. Never stop or change a blood thinner for testing unless the prescribing clinician specifically tells you to do so.
What does triple-positive antiphospholipid testing mean?
Triple positivity means that lupus anticoagulant, anticardiolipin, and anti-β2-glycoprotein I antibodies are all positive and remain positive on repeat testing. This pattern is associated with the highest clinical risk among the antibody profiles, but your personal risk also depends on your history, including prior clots and other health conditions.
What is the lupus anticoagulant test measuring?
Lupus anticoagulant is a functional blood test that measures how long blood takes to clot in the laboratory, often using tests such as dRVVT or aPTT. It is usually reported as positive or negative rather than as an IgG or IgM level, and its name does not mean it is a test for lupus.

Questions to Ask Your Doctor

Curated prompts to bring to your next appointment.

  1. 1.Which of the three core APS tests (LA, aCL, or anti-β2GPI) were positive, and what is my overall antibody profile?
  2. 2.Are my results based on the laboratory's specific cutoff, or do they meet the medium/high thresholds used in clinical criteria?
  3. 3.How do my current medications, including any blood thinners, affect the accuracy of my Lupus Anticoagulant (LA) results?
  4. 4.When should we schedule my 12-week repeat testing, and do we need to use the exact same laboratory to ensure the results are comparable?

Questions For You

Tap a prompt to share your answer — we'll use it plus this page's context to start a tailored conversation.

References

References (12)
  1. 1

    Cardiac Manifestations of Antiphospholipid Syndrome: Clinical Presentation, Role of Cardiac Imaging, and Treatment Strategies.

    Tufano A, Di Minno MND, Guida A, et al.

    Seminars in thrombosis and hemostasis 2019; (45(5)):468-477 doi:10.1055/s-0039-1692702.

    PMID: 31216589
  2. 2

    Laboratory Diagnosis of Antiphospholipid Syndrome: Insights and Hindrances.

    Vandevelde A, Devreese KMJ

    Journal of clinical medicine 2022; (11(8)) doi:10.3390/jcm11082164.

    PMID: 35456258
  3. 3

    The role of different aPL subpopulations in the lupus anticoagulant phenomenon.

    Arachchillage DJ, Efthymiou M, Cohen H

    Current opinion in immunology 2026; (100()):102784 doi:10.1016/j.coi.2026.102784.

    PMID: 42085810
  4. 4

    Antiphospholipid Syndrome: Thrombotic and Vascular Complications.

    Windisch S, Ash JY, Frishman WH

    Cardiology in review 2025; (33(2)):139-144 doi:10.1097/CRD.0000000000000590.

    PMID: 37607079
  5. 5

    Brief Report: Changes in Antiphospholipid Antibody Titers During Pregnancy: Effects on Pregnancy Outcomes.

    Yelnik CM, Porter TF, Branch DW, et al.

    Arthritis & rheumatology (Hoboken, N.J.) 2016; (68(8)):1964-9 doi:10.1002/art.39668.

    PMID: 26990620
  6. 6

    An update on laboratory detection and interpretation of antiphospholipid antibodies for diagnosis of antiphospholipid syndrome: guidance from the ISTH-SSC Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibodies.

    Devreese KMJ, Bertolaccini ML, Branch DW, et al.

    Journal of thrombosis and haemostasis : JTH 2025; (23(2)):731-744 doi:10.1016/j.jtha.2024.10.022.

    PMID: 39510414
  7. 7

    New ACR/EULAR 2023 classification criteria for antiphospholipid syndrome, what should a gynaecologist know in 2025.

    Murarasu A, de Frémont GM, Guettrot-Imbert G, et al.

    Journal of gynecology obstetrics and human reproduction 2026; (55(2)):103095 doi:10.1016/j.jogoh.2025.103095.

    PMID: 41422861
  8. 8

    Reporting and Establishment of Reference Intervals for Antiphospholipid Antibody Immunoassays: A Survey of Participants in the College of American Pathologists Proficiency Testing Program.

    Tebo AE, Willis R, Nwosu A, et al.

    Archives of pathology & laboratory medicine 2024; (148(6)):686-693 doi:10.5858/arpa.2023-0095-CP.

    PMID: 37756558
  9. 9

    Systematic review of case reports of antiphospholipid syndrome following infection.

    Abdel-Wahab N, Lopez-Olivo MA, Pinto-Patarroyo GP, Suarez-Almazor ME

    Lupus 2016; (25(14)):1520-1531 doi:10.1177/0961203316640912.

    PMID: 27060064
  10. 10

    Testing for the lupus anticoagulant: the good, the bad, and the ugly.

    Favaloro EJ, Pasalic L, Selby R

    Research and practice in thrombosis and haemostasis 2024; (8(3)):102385 doi:10.1016/j.rpth.2024.102385.

    PMID: 38623474
  11. 11

    Antiphospholipid syndrome.

    Sammaritano LR

    Best practice & research. Clinical rheumatology 2020; (34(1)):101463 doi:10.1016/j.berh.2019.101463.

    PMID: 31866276
  12. 12

    Obstetric antiphospholipid syndrome.

    Antovic A, Sennström M, Bremme K, Svenungsson E

    Lupus science & medicine 2018; (5(1)):e000197 doi:10.1136/lupus-2016-000197.

    PMID: 30364418

This page is for informational purposes only and does not constitute medical advice or diagnose antiphospholipid syndrome. Your clinician should interpret your results, medications, and clinical history.

Get notified when new evidence is published on familial antiphospholipid syndrome.

We monitor PubMed for new peer-reviewed studies on this topic and email a short summary when something meaningful changes.