Lupus & antiphospholipid syndrome

Clinical, serological and haemodynamic factors associated with poor outcomes in systemic lupus erythematosus-associated pulmonary arterial hypertension: a multicentre retrospective study from Korea

Rheumatology (Oxford)Published Retrospective cohort study

Authors' conclusion

Elevated mPAP, active lupus and use of combination PAH therapy were independently associated with poor outcomes in SLE-PAH

Study context

Population
Korean patients with SLE-associated PAH confirmed by right heart catheterization, eight tertiary centres
Participants
68 patients
Exposure
Patients with vs without composite outcomes
  • Composite outcomesn = 35
Outcome
Composite of:
  • Worsening PAH symptoms requiring treatment escalation
  • Lung transplantation
  • Death
  • Hospitalization
Methodological detailsmulticentre, univariable and multivariable logistic regression
  • Multicentre
  • Univariable and multivariable logistic regression

Main finding

As reported in the abstract

Composite outcome

Composite outcomes

51.3%

35

Independent predictor (multivariable): elevated mean pulmonary arterial pressure (mPAP), OR 5.401 (95% CI 1.129-25.837)
P = 0.035
Independent predictor (multivariable): higher SLE Disease Activity Index (SLEDAI), OR 5.495 (95% CI 1.041-29.012)
P = 0.045
Independent predictor (multivariable): combination PAH therapy, OR 1.695 (95% CI 1.015-3.267)
P = 0.017

Observational data: associations, not effects.

Further findings

Univariable differences, composite outcomes vs without

Shorter baseline 6-min walk distance
P = 0.024
Higher tricuspid regurgitation velocity
P = 0.032
Higher right ventricular systolic pressure
P = 0.035
Higher mPAP
P < 0.001
Higher mean PGA scores
P = 0.001
Higher mean SLEDAI scores
P = 0.005
More frequent combination PAH therapy
P = 0.033

Original publication

Clinical, serological and haemodynamic factors associated with poor outcomes in systemic lupus erythematosus-associated pulmonary arterial hypertension: a multicentre retrospective study from Korea. Rheumatology (Oxford). Published 30 March 2026. doi:10.1093/rheumatology/keag148

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