Lupus & antiphospholipid syndrome

A one-point increase in the Damage Index for Antiphospholipid Syndrome (DIAPS) predicts mortality in thrombotic antiphospholipid syndrome

Clin Exp RheumatolPublished Retrospective cohort study

Main finding · MortalityResult — go to the resultHazard ratio 5.40 95% CI 2.33–12.52

Authors' conclusion

Evolving damage in the first five years of illness, but not early damage, predicted mortality regardless of the nature of the first thrombotic event, sex, APS category and age.

Study context

Population
Thrombotic APS patients (2006 Sydney criteria), single centre; 71.1% female, 65.9% primary APS, 72.4% Caucasianfollowed up to 43 years (median 10)
Participants
197 patients
Exposure
Early damage and early damage increase (delta-DIAPS) vs none, as predictors of mortality
  • Delta-DIAPSn = 53/181
  • Early damagen = 69
Outcome
Mortality
Methodological detailssingle-centre, Kaplan-Meier survival analysis, Cox regression
  • Single-centre
  • Kaplan-Meier survival analysis
  • Cox regression

Main finding

As reported in the abstract

Hazard ratio

5.40

95% CI 2.33–12.52

P < 0.001

Delta-DIAPS
HR 5.40 (95% CI 2.33–12.52); P < 0.001
Deaths
23 (12%)

Observational data: associations, not effects.

Further findings

Risk factors for death

HR (95% CI)P value
Secondary APS3.07 (1.32–7.12)P = 0.009
Male sex3.14 (1.35–7.33)P = 0.008
Age at APS onset ≥40 years5.34 (1.96–14.53)P = 0.001
OutcomeP value
First arterial event: association with early damage, delta-DIAPS and deathFirst arterial eventP < 0.001
First arterial event: association with early damage, delta-DIAPS and deathFirst arterial event · not associatedP = 0.539
First arterial event: association with early damage, delta-DIAPS and deathFirst arterial event · not associatedP = 0.151

Damage development

Damage developed
143 (73.6%)

Original publication

A one-point increase in the Damage Index for Antiphospholipid Syndrome (DIAPS) predicts mortality in thrombotic antiphospholipid syndrome. Clin Exp Rheumatol. Published 28 February 2022. doi:10.55563/clinexprheumatol/0gs167

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