Lupus & antiphospholipid syndrome

Significance of the weighted complement domain of the EULAR/ACR classification criteria in juvenile onset systemic lupus erythematosus

LupusPublished Retrospective cohort study

Authors' conclusion

Observation of more frequent clinical and serological activity with higher total scores from the EULAR/ACR classification criteria supported the higher scoring of patients with low C3 and C4 in the weighted criteria.

Study context

Population
Patients with juvenile onset SLE fulfilling the 2019 EULAR/ACR classification criteria
Participants
43 patients
Exposure
Low C3 and C4 vs other complement status at onset
Outcome
Hypocomplementemia
Follow-up
Disease onset

Main finding

As reported in the abstract

Observational data: associations, not effects.

Further findings

OutcomeValuesP value
Cutaneous involvementvs 28.6%Low C3 and C4 65.2%p: 0.045
Musculoskeletal involvementvs 42.9%Low C3 and C4 78.3%p: 0.039
Autoimmune hemolytic anemiavs 14.3%Low C3 and C4 52.2%p: 0.035
Positive anti-dsDNAvs 21.4%Low C3 and C4 65.2%p: 0.017
Anti-Sm antibodiesvs 21.4%Low C3 and C4 60.9%p: 0.04
2019 EULAR/ACR classification criteria scorevs 15.5Low C3 and C4 26p: < 0.0001

Remission, flare rates and SLE-associated damage (patients with hypocomplementemia)

Did not differ according to complement status

Original publication

Significance of the weighted complement domain of the EULAR/ACR classification criteria in juvenile onset systemic lupus erythematosus. Lupus. Published 17 April 2023. doi:10.1177/09612033231171343

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