Lupus & antiphospholipid syndrome

Immune thrombocytopenia is rare in patients with antiphospholipid syndrome without systemic lupus erythematosus: insights from a series of 351 patients

Lupus Sci MedPublished Retrospective cohort study

Authors' conclusion

In patients with APS, the underlying cause of thrombocytopenia can be identified in most cases through careful review of medical records. True ITP is uncommon and appears to be exceptionally rare in patients with APS without concomitant SLE.

Study context

Population
Patients with antiphospholipid syndrome (APS) with at least one episode of thrombocytopenia (platelet count <100 x 10ˆ9/L), tertiary referral cohort102 with thrombocytopenia included
Participants
351 patients
Exposure
Catastrophic antiphospholipid syndrome (CAPS) vs immune thrombocytopenia (ITP)
  • CAPSn = 75reference
  • ITPn = 12
Outcome
Aetiologies of thrombocytopenia and frequency and characteristics of ITP, including association with SLE
Methodological detailssingle-centre tertiary referral cohort, enriched in severe cases
  • Single-centre tertiary referral cohort
  • Enriched in severe cases

Main finding

As reported in the abstract

Causes of thrombocytopenia
Thrombocytopenia among APS patients
102 (29.1%)
CAPS
n=75, 73.5%
ITP (including two with both CAPS and ITP)
n=12, 11.8%
Other identified causes
11 (10.8%)
Unexplained
six patients (5.9%)
Isolated ITP without SLE, share of entire APS cohort
0.6%

Observational data: associations, not effects.

Further findings

Associated SLE

P = 0.013

Platelet nadir and severity

Median platelet nadir (x 10ˆ9/L)
34.5
Severe thrombocytopenia (<20 x 10ˆ9/L)
33 (32.4%)

Safety

OutcomeHR (95% CI)
Severe haemorrhagic events, platelet nadir <20vs >100 x 10ˆ9/LGraded increase with severity; not statistically significant2.55 (0.94–6.94)

Original publication

Immune thrombocytopenia is rare in patients with antiphospholipid syndrome without systemic lupus erythematosus: insights from a series of 351 patients. Lupus Sci Med. Published 11 August 2026. doi:10.1136/lupus-2026-002084

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