Lupus & antiphospholipid syndrome

High burden and unique pattern of cerebral small vessel disease in antiphospholipid syndrome: MRI subtypes and risk profile in a large cohort

LupusPublished Retrospective cohort study

Authors' conclusion

cSVD is a common feature in patients with APS and often occurs in the absence of neurological manifestations.

Study context

Population
Patients with antiphospholipid syndrome (APS) and age- and sex-matched healthy controls132 APS patients
Exposure
APS vs age- and sex-matched healthy controls
  • APSn = 132
Outcome
Burden and MRI subtypes of cerebral small vessel disease (cSVD; lacunes, EPVS, microbleeds, WMH; total cSVD score 0-4)
Methodological detailsage- and sex-matched healthy controls, logistic regression adjusted for age, sex and disease duration
  • Age- and sex-matched healthy controls
  • Logistic regression adjusted for age, sex and disease duration

Main finding

As reported in the abstract

cSVD in APS
GroupValueLacunesWhite matter hyperintensities (WMH)Enlarged perivascular spaces (EPVS)Microbleeds
APS51.5%46.2%16.7%14.4%12.1%

APS

Value51.5%
Lacunes46.2%
White matter hyperintensities (WMH)16.7%
Enlarged perivascular spaces (EPVS)14.4%
Microbleeds12.1%
History of stroke
24.2%

Observational data: associations, not effects.

Further findings

Factors independently associated with cerebral small vessel disease (cSVD) in APS

OR (95% CI)P value
HypertensionAdjusted for age, sex, and disease duration3.69 (1.17–11.65)P = 0.026
Prior thrombosisAdjusted for age, sex, and disease duration22.15 (2.11–232.27)P = 0.010
Prior strokeAdjusted for age, sex, and disease duration10.71 (2.47–46.36)P = 0.002
Subclinical cSVD in APS without neurological symptoms
34.8%

Factors independently associated with cSVD in APS

Individual aPL profiles not independently associated with cSVD

Original publication

High burden and unique pattern of cerebral small vessel disease in antiphospholipid syndrome: MRI subtypes and risk profile in a large cohort. Lupus. Published 29 September 2026. doi:10.1177/09612033261494025

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