Vial

INDIVIDUAL TEST 517

Beta-2-Glycoprotein 1 Antibodies (IgG, IgM)

Indication

Suspicion of primary antiphospholipid syndrome (APS) and systemic lupus erythematous with secondary antiphospholipid syndrome (APS)

Sample material

Serum

  • Minim. volume: 0,5 mL

Transport

  • Within Sweden: room temperature
  • International: cold

Method

ELISA

Reference interval

< 20 U/mL negative

Result

Results are reported as negative or positive with a concentration (U/mL).

Interpretation

Elevated levels of IgM and IgG antibodies against Beta-2-Glycoprotein-1 are included in the laboratory criteria for the antiphospholipid syndrome (APS), characterized by thrombotic tendency (arterial and/or venous), and/or pregnancy morbidity (miscarriage/preeclampsia/placental insufficiency).

The syndrome can be associated with SLE (secondary APS) but also occurs without signs of inflammatory systemic disease (primary APS). The highest risk for APS is triple positivity, i.e., the presence of antibodies against Beta-2-Glycoprotein-1 in combination with lupus anticoagulant and antibodies against Cardiolipin.

References

  • Barbhaiya M et al. Ann Rheum Dis. 2023. 2023 ACR/EULAR antiphospholipid syndrome classification criteria. PMID: 37640450
  • Cabrera-Marante O et al. Front Immunol. 2025. Criteria and non-criteria anti-phospholipid antibodies in the different clinical forms of antiphospholipid syndrome. PMID: 40821829
  • Van Hoovels L et al. J Thromb Haemost. 2025. Multicenter study to improve clinical interpretation of anticardiolipin and anti-β2-glycoprotein I antibody test results for diagnosis of antiphospholipid syndrome. PMID: 40383153

Last updated: 2025-12-01

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Vial

ENSKILD ANALYS 517

Beta-2-Glykoprotein 1-antikroppar (IgG, IgM)

Indikation

Misstanke om primärt antifosfolipidsyndrom (APS) och systemisk lupus erytematosus.

Provmaterial

Serum

  • Minim. volym: 0,5 mL

Transport

  • Inom Sverige: rumstemperatur
  • Internationellt: kylt

Metod

ELISA

Referensintervall

< 20 U/mL negativt

Resultat

Resultatet anges som negativt eller positivt med koncentration (U/mL).

Tolkning

Förhöjda nivåer av IgG- och IgM-antikroppar mot beta-2-glykoprotein-1 ingår i laboratoriekriterierna för antifosfolipidsyndrom (APS) som karakteriseras av trombosbenägenhet (arteriell och/eller venös) och/eller graviditetsmorbiditet (missfall/preeklampsi/placentainsufficiens).

Syndromet kan vara associerat med SLE (sekundärt APS), men förekommer även utan tecken på inflammatorisk systemsjukdom (primärt APS). Högst risk för APS utgör trippelpositivitet dvs förekomst av antikroppar mot beta-2-glykoprotein-1 i kombination med lupus antikoagulans och antikroppar mot kardiolipin.

Referenser

  • Barbhaiya M et al. Ann Rheum Dis. 2023. 2023 ACR/EULAR antiphospholipid syndrome classification criteria. PMID: 37640450
  • Cabrera-Marante O et al. Front Immunol. 2025. Criteria and non-criteria anti-phospholipid antibodies in the different clinical forms of antiphospholipid syndrome. PMID: 40821829
  • Van Hoovels L et al. J Thromb Haemost. 2025. Multicenter study to improve clinical interpretation of anticardiolipin and anti-β2-glycoprotein I antibody test results for diagnosis of antiphospholipid syndrome. PMID: 40383153

Senast uppdaterat: 2025-12-01

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