High sensitivity C-reactive protein in systemic lupus erythematosus: relation to disease activity, clinical

E V Barnes1, S Narain, A Naranjo

  • 1Department of Medicine, Division of Rheumatology & Clinical Immunology, University of Florida, Gainesville, FL 32610-0221, USA.

Lupus
|September 24, 2005
PubMed

Insights

High sensitivity C-reactive protein (hs-CRP) does not effectively track disease activity in systemic lupus erythematosus (SLE). However, hs-CRP may help assess cardiovascular risk in SLE patients, with antimalarials potentially reducing this risk.

Area of Science:

  • Rheumatology
  • Immunology
  • Cardiovascular Medicine

Background:

  • High sensitivity C-reactive protein (hs-CRP) is utilized in assessing rheumatic disease activity.
  • Its specific utility in systemic lupus erythematosus (SLE) for disease activity, severity, and cardiovascular risk assessment remains uncertain.

Purpose of the Study:

  • To investigate the role of hs-CRP in evaluating disease activity, severity, and cardiovascular risk in SLE patients.
  • To determine the correlation between hs-CRP levels and established cardiovascular risk factors within the SLE cohort.

Main Methods:

  • Serum samples from 213 SLE patients (601 visits) and 134 controls were analyzed for hs-CRP using nephelometry.
  • Demographic data, medication history, and laboratory parameters were collected.
  • Disease activity was quantified using the SLE Disease Activity Index (SLEDAI).

Main Results:

  • hs-CRP levels showed no association with SLEDAI scores, ACR SLE criteria, or specific organ involvement.
  • hs-CRP levels significantly correlated with cardiovascular risk factors: body weight, hypertension, and apolipoprotein A-I.
  • An inverse correlation was observed between hs-CRP levels and the use of antimalarial medications.

Conclusions:

  • hs-CRP is not a reliable marker for assessing disease activity in SLE.
  • hs-CRP may hold value in evaluating cardiovascular risk in SLE patients.
  • Antimalarial use might contribute to reduced cardiovascular risk in individuals with SLE.

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